TY  - JOUR
AU  - Vajs, Vlatka
AU  - Jeremić, Dragoslav
AU  - Milosavljević, Slobodan
AU  - Macura, Slobodan
PY  - 1989
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2792
AB  - The isolation of 11(13)-dehydrocriolin [a germacranolide also known as 11(13)-dehydroivaxillin], 2α-hydroxyalantolactone, 4α,5α-epoxy-10α,14-H-inuviscolide (the major component) and carabrone from the aerial parts of Inula helenium is reported. The first two lactones were isolated for the first time from this plant. © 1989.
PB  - Pergamon Press
T2  - Phytochemistry
T1  - Sesquiterpene lactones from Inula helenium
VL  - 28
IS  - 6
SP  - 1763
EP  - 1764
DO  - 10.1016/S0031-9422(00)97842-7
ER  - 

@article{
author = "Vajs, Vlatka and Jeremić, Dragoslav and Milosavljević, Slobodan and Macura, Slobodan",
year = "1989",
abstract = "The isolation of 11(13)-dehydrocriolin [a germacranolide also known as 11(13)-dehydroivaxillin], 2α-hydroxyalantolactone, 4α,5α-epoxy-10α,14-H-inuviscolide (the major component) and carabrone from the aerial parts of Inula helenium is reported. The first two lactones were isolated for the first time from this plant. © 1989.",
publisher = "Pergamon Press",
journal = "Phytochemistry",
title = "Sesquiterpene lactones from Inula helenium",
volume = "28",
number = "6",
pages = "1763-1764",
doi = "10.1016/S0031-9422(00)97842-7"
}

Vajs, V., Jeremić, D., Milosavljević, S.,& Macura, S.. (1989). Sesquiterpene lactones from Inula helenium. in Phytochemistry
Pergamon Press., 28(6), 1763-1764.
https://doi.org/10.1016/S0031-9422(00)97842-7

Vajs V, Jeremić D, Milosavljević S, Macura S. Sesquiterpene lactones from Inula helenium. in Phytochemistry. 1989;28(6):1763-1764.
doi:10.1016/S0031-9422(00)97842-7 .

Vajs, Vlatka, Jeremić, Dragoslav, Milosavljević, Slobodan, Macura, Slobodan, "Sesquiterpene lactones from Inula helenium" in Phytochemistry, 28, no. 6 (1989):1763-1764,
https://doi.org/10.1016/S0031-9422(00)97842-7 . .

TY  - JOUR
AU  - Janković, B D
AU  - Korolija, P
AU  - Isaković, K
AU  - Popesković, L J
AU  - Pešić, M. Č.
AU  - Horvat, J
AU  - Jeremić, Dragoslav
AU  - Vajs, Vlatka
PY  - 1988
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2793
PB  - The New York Academy of Sciences
T2  - Annals of the New York Academy of Sciences
T1  - Immunorestorative Effects in Elderly Humans of Lipid and Protein Fractions from the Calf Thymus: A Double‐Blind Study
VL  - 521
IS  - 1
SP  - 247
EP  - 259
DO  - 10.1111/j.1749-6632.1988.tb35283.x
ER  - 

@article{
author = "Janković, B D and Korolija, P and Isaković, K and Popesković, L J and Pešić, M. Č. and Horvat, J and Jeremić, Dragoslav and Vajs, Vlatka",
year = "1988",
publisher = "The New York Academy of Sciences",
journal = "Annals of the New York Academy of Sciences",
title = "Immunorestorative Effects in Elderly Humans of Lipid and Protein Fractions from the Calf Thymus: A Double‐Blind Study",
volume = "521",
number = "1",
pages = "247-259",
doi = "10.1111/j.1749-6632.1988.tb35283.x"
}

Janković, B. D., Korolija, P., Isaković, K., Popesković, L. J., Pešić, M. Č., Horvat, J., Jeremić, D.,& Vajs, V.. (1988). Immunorestorative Effects in Elderly Humans of Lipid and Protein Fractions from the Calf Thymus: A Double‐Blind Study. in Annals of the New York Academy of Sciences
The New York Academy of Sciences., 521(1), 247-259.
https://doi.org/10.1111/j.1749-6632.1988.tb35283.x

Janković BD, Korolija P, Isaković K, Popesković LJ, Pešić MČ, Horvat J, Jeremić D, Vajs V. Immunorestorative Effects in Elderly Humans of Lipid and Protein Fractions from the Calf Thymus: A Double‐Blind Study. in Annals of the New York Academy of Sciences. 1988;521(1):247-259.
doi:10.1111/j.1749-6632.1988.tb35283.x .

Janković, B D, Korolija, P, Isaković, K, Popesković, L J, Pešić, M. Č., Horvat, J, Jeremić, Dragoslav, Vajs, Vlatka, "Immunorestorative Effects in Elderly Humans of Lipid and Protein Fractions from the Calf Thymus: A Double‐Blind Study" in Annals of the New York Academy of Sciences, 521, no. 1 (1988):247-259,
https://doi.org/10.1111/j.1749-6632.1988.tb35283.x . .

TY  - JOUR
AU  - Vajs, Vlatka
AU  - Jeremić, Dragoslav
AU  - Milosavljević, Slobodan
AU  - Macura, Slobodan
PY  - 1987
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2784
AB  - The application of two‐dimensional NOE NMR spectroscopy (NOESY) for the stereochemical assignment of isomeric 14‐acetoxy‐13‐hydroxy‐ and 13‐acetoxy‐14‐hydroxy‐5,6‐caryophyllen‐7‐ones, and their acetylation products, is reported. Copyright © 1987 John Wiley & Sons Ltd.
PB  - John Wiley & Sons Ltd.
T2  - Magnetic Resonance in Chemistry
T1  - Two‐dimensional NMR spectra of sesquiterpenes. I—NOESY study of caryophyllenes from Inula spiraeifolia
VL  - 25
IS  - 10
SP  - 889
EP  - 891
DO  - 10.1002/mrc.1260251012
ER  - 

@article{
author = "Vajs, Vlatka and Jeremić, Dragoslav and Milosavljević, Slobodan and Macura, Slobodan",
year = "1987",
abstract = "The application of two‐dimensional NOE NMR spectroscopy (NOESY) for the stereochemical assignment of isomeric 14‐acetoxy‐13‐hydroxy‐ and 13‐acetoxy‐14‐hydroxy‐5,6‐caryophyllen‐7‐ones, and their acetylation products, is reported. Copyright © 1987 John Wiley & Sons Ltd.",
publisher = "John Wiley & Sons Ltd.",
journal = "Magnetic Resonance in Chemistry",
title = "Two‐dimensional NMR spectra of sesquiterpenes. I—NOESY study of caryophyllenes from Inula spiraeifolia",
volume = "25",
number = "10",
pages = "889-891",
doi = "10.1002/mrc.1260251012"
}

Vajs, V., Jeremić, D., Milosavljević, S.,& Macura, S.. (1987). Two‐dimensional NMR spectra of sesquiterpenes. I—NOESY study of caryophyllenes from Inula spiraeifolia. in Magnetic Resonance in Chemistry
John Wiley & Sons Ltd.., 25(10), 889-891.
https://doi.org/10.1002/mrc.1260251012

Vajs V, Jeremić D, Milosavljević S, Macura S. Two‐dimensional NMR spectra of sesquiterpenes. I—NOESY study of caryophyllenes from Inula spiraeifolia. in Magnetic Resonance in Chemistry. 1987;25(10):889-891.
doi:10.1002/mrc.1260251012 .

Vajs, Vlatka, Jeremić, Dragoslav, Milosavljević, Slobodan, Macura, Slobodan, "Two‐dimensional NMR spectra of sesquiterpenes. I—NOESY study of caryophyllenes from Inula spiraeifolia" in Magnetic Resonance in Chemistry, 25, no. 10 (1987):889-891,
https://doi.org/10.1002/mrc.1260251012 . .

TY  - JOUR
AU  - Jeremić, Dragoslav
AU  - Macura, Slobodan
AU  - Milosavljević, Slobodan
AU  - Vajs, Vlatka
PY  - 1985
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2786
AB  - Identification of a novel trioxygenated Δ8(9),15_ pimaric acid methyl ester from plant species Lycopus europaeus by means of two-dimensional 1H NMR spectroscopy (COSY and NOESY) is reported. © 1985.
PB  - Pergamon Press
T2  - Tetrahedron
T1  - A novel pimara-8(9),15-diene from lycopus europaeus
VL  - 41
IS  - 2
SP  - 357
EP  - 364
DO  - 10.1016/S0040-4020(01)96427-0
ER  - 

@article{
author = "Jeremić, Dragoslav and Macura, Slobodan and Milosavljević, Slobodan and Vajs, Vlatka",
year = "1985",
abstract = "Identification of a novel trioxygenated Δ8(9),15_ pimaric acid methyl ester from plant species Lycopus europaeus by means of two-dimensional 1H NMR spectroscopy (COSY and NOESY) is reported. © 1985.",
publisher = "Pergamon Press",
journal = "Tetrahedron",
title = "A novel pimara-8(9),15-diene from lycopus europaeus",
volume = "41",
number = "2",
pages = "357-364",
doi = "10.1016/S0040-4020(01)96427-0"
}

Jeremić, D., Macura, S., Milosavljević, S.,& Vajs, V.. (1985). A novel pimara-8(9),15-diene from lycopus europaeus. in Tetrahedron
Pergamon Press., 41(2), 357-364.
https://doi.org/10.1016/S0040-4020(01)96427-0

Jeremić D, Macura S, Milosavljević S, Vajs V. A novel pimara-8(9),15-diene from lycopus europaeus. in Tetrahedron. 1985;41(2):357-364.
doi:10.1016/S0040-4020(01)96427-0 .

Jeremić, Dragoslav, Macura, Slobodan, Milosavljević, Slobodan, Vajs, Vlatka, "A novel pimara-8(9),15-diene from lycopus europaeus" in Tetrahedron, 41, no. 2 (1985):357-364,
https://doi.org/10.1016/S0040-4020(01)96427-0 . .

TY  - JOUR
AU  - Došen-Mićović, Ljiljana
AU  - Jeremić, Dragoslav
AU  - Allinger, Norman L.
PY  - 1983
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4218
AB  - A model of intramolecular electrostatic effects (called the induced dipole moment and energy (IDME) method) was derived by extending the method originally proposed by Del Re for calculating dipole moments and charge distributions. The IDME procedure consists of taking bond dipoles, calculated by the Del Re procedure, and allowing for nonadjacent dipole interactions by taking all components of bond polarizabilities into account. The method is applied to some simple halides, ketones, and ethers. The total dipole moments are well calculated and charge distributions reproduce many known trends. The calculated energies agree better with experiment overall than those calculated earlier by the modified Smith-Eyring method.
PB  - American Chemical Society (ACS)
T2  - Journal of the American Chemical Society
T1  - Treatment of electrostatic effects within the molecular mechanics method. 1
VL  - 105
IS  - 7
SP  - 1716
EP  - 1722
DO  - 10.1021/ja00345a003
ER  - 

@article{
author = "Došen-Mićović, Ljiljana and Jeremić, Dragoslav and Allinger, Norman L.",
year = "1983",
abstract = "A model of intramolecular electrostatic effects (called the induced dipole moment and energy (IDME) method) was derived by extending the method originally proposed by Del Re for calculating dipole moments and charge distributions. The IDME procedure consists of taking bond dipoles, calculated by the Del Re procedure, and allowing for nonadjacent dipole interactions by taking all components of bond polarizabilities into account. The method is applied to some simple halides, ketones, and ethers. The total dipole moments are well calculated and charge distributions reproduce many known trends. The calculated energies agree better with experiment overall than those calculated earlier by the modified Smith-Eyring method.",
publisher = "American Chemical Society (ACS)",
journal = "Journal of the American Chemical Society",
title = "Treatment of electrostatic effects within the molecular mechanics method. 1",
volume = "105",
number = "7",
pages = "1716-1722",
doi = "10.1021/ja00345a003"
}

Došen-Mićović, L., Jeremić, D.,& Allinger, N. L.. (1983). Treatment of electrostatic effects within the molecular mechanics method. 1. in Journal of the American Chemical Society
American Chemical Society (ACS)., 105(7), 1716-1722.
https://doi.org/10.1021/ja00345a003

Došen-Mićović L, Jeremić D, Allinger NL. Treatment of electrostatic effects within the molecular mechanics method. 1. in Journal of the American Chemical Society. 1983;105(7):1716-1722.
doi:10.1021/ja00345a003 .

Došen-Mićović, Ljiljana, Jeremić, Dragoslav, Allinger, Norman L., "Treatment of electrostatic effects within the molecular mechanics method. 1" in Journal of the American Chemical Society, 105, no. 7 (1983):1716-1722,
https://doi.org/10.1021/ja00345a003 . .

TY  - JOUR
AU  - Došen-Mićović, Ljiljana
AU  - Jeremić, Dragoslav
AU  - Allinger, Norman L.
PY  - 1983
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4428
AB  - The previously developed general method, which includes induction by dipoles in polarizable bonds and the solvation of molecular dipoles and quadrupoles, was used to calculate molecular dipole moments and to predict conformational equilibria of polar compounds, both in the gas phase and in solution. The results are in good agreement with experimentally determined values for 35 compounds including dihalides, halo ketones, and halo ethers. More simplified calculations often lead to erroneous predictions of conformational equilibria.
PB  - American Chemical Society
T2  - Journal of the American Chemical Society
T1  - Treatment of electrostatic effects within the molecular mechanics Method. 2
VL  - 105
IS  - 7
SP  - 1723
EP  - 1733
DO  - 10.1021/ja00345a004
ER  - 

@article{
author = "Došen-Mićović, Ljiljana and Jeremić, Dragoslav and Allinger, Norman L.",
year = "1983",
abstract = "The previously developed general method, which includes induction by dipoles in polarizable bonds and the solvation of molecular dipoles and quadrupoles, was used to calculate molecular dipole moments and to predict conformational equilibria of polar compounds, both in the gas phase and in solution. The results are in good agreement with experimentally determined values for 35 compounds including dihalides, halo ketones, and halo ethers. More simplified calculations often lead to erroneous predictions of conformational equilibria.",
publisher = "American Chemical Society",
journal = "Journal of the American Chemical Society",
title = "Treatment of electrostatic effects within the molecular mechanics Method. 2",
volume = "105",
number = "7",
pages = "1723-1733",
doi = "10.1021/ja00345a004"
}

Došen-Mićović, L., Jeremić, D.,& Allinger, N. L.. (1983). Treatment of electrostatic effects within the molecular mechanics Method. 2. in Journal of the American Chemical Society
American Chemical Society., 105(7), 1723-1733.
https://doi.org/10.1021/ja00345a004

Došen-Mićović L, Jeremić D, Allinger NL. Treatment of electrostatic effects within the molecular mechanics Method. 2. in Journal of the American Chemical Society. 1983;105(7):1723-1733.
doi:10.1021/ja00345a004 .

Došen-Mićović, Ljiljana, Jeremić, Dragoslav, Allinger, Norman L., "Treatment of electrostatic effects within the molecular mechanics Method. 2" in Journal of the American Chemical Society, 105, no. 7 (1983):1723-1733,
https://doi.org/10.1021/ja00345a004 . .

TY  - JOUR
AU  - Jeremić, Dragoslav
AU  - Milosavljević, Slobodan
AU  - Vajs, Vlatka
PY  - 1982
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2787
AB  - The identification of two novel isomeric trioxygenated caryophyllenes from the plant species Inula Spiraefolia is reported. © 1982.
PB  - Pergamon Press
T2  - Tetrahedron Letters
T1  - Novel trioxygenated caryophyllenes from Inula Spiraefolia
VL  - 23
IS  - 9
SP  - 1009
EP  - 1012
DO  - 10.1016/S0040-4039(00)87007-0
ER  - 

@article{
author = "Jeremić, Dragoslav and Milosavljević, Slobodan and Vajs, Vlatka",
year = "1982",
abstract = "The identification of two novel isomeric trioxygenated caryophyllenes from the plant species Inula Spiraefolia is reported. © 1982.",
publisher = "Pergamon Press",
journal = "Tetrahedron Letters",
title = "Novel trioxygenated caryophyllenes from Inula Spiraefolia",
volume = "23",
number = "9",
pages = "1009-1012",
doi = "10.1016/S0040-4039(00)87007-0"
}

Jeremić, D., Milosavljević, S.,& Vajs, V.. (1982). Novel trioxygenated caryophyllenes from Inula Spiraefolia. in Tetrahedron Letters
Pergamon Press., 23(9), 1009-1012.
https://doi.org/10.1016/S0040-4039(00)87007-0

Jeremić D, Milosavljević S, Vajs V. Novel trioxygenated caryophyllenes from Inula Spiraefolia. in Tetrahedron Letters. 1982;23(9):1009-1012.
doi:10.1016/S0040-4039(00)87007-0 .

Jeremić, Dragoslav, Milosavljević, Slobodan, Vajs, Vlatka, "Novel trioxygenated caryophyllenes from Inula Spiraefolia" in Tetrahedron Letters, 23, no. 9 (1982):1009-1012,
https://doi.org/10.1016/S0040-4039(00)87007-0 . .

TY  - JOUR
AU  - Milosavljević, Slobodan
AU  - Jeremić, Dragoslav
AU  - Mihailović, Milhailo Lj.
AU  - Wehrli, Felix W.
PY  - 1981
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4421
AB  - Unambiguous signal assignments in the 13C spectra of monodeuterated cyclooctanones derived from the lead tetraacetate or silver oxide/bromine oxidations of the corresponding 1‐monodeutero‐alcohols have been obtained from deuterium‐induced 13C isotope shifts and geminal and vicinal 13C-2H spin‐spin coupling constants. The label in the ketones is shown to be in position 5.
PB  - Wiley
T2  - Organic Magnetic Resonance
T1  - Deuterium‐induced 13C nuclear magnetic resonance isotope shifts and 13C-2H couplings for signal assignments and determination of deuteration site in cyclooctanone
VL  - 17
IS  - 4
SP  - 299
EP  - 300
DO  - 10.1002/mrc.1270170415
ER  - 

@article{
author = "Milosavljević, Slobodan and Jeremić, Dragoslav and Mihailović, Milhailo Lj. and Wehrli, Felix W.",
year = "1981",
abstract = "Unambiguous signal assignments in the 13C spectra of monodeuterated cyclooctanones derived from the lead tetraacetate or silver oxide/bromine oxidations of the corresponding 1‐monodeutero‐alcohols have been obtained from deuterium‐induced 13C isotope shifts and geminal and vicinal 13C-2H spin‐spin coupling constants. The label in the ketones is shown to be in position 5.",
publisher = "Wiley",
journal = "Organic Magnetic Resonance",
title = "Deuterium‐induced 13C nuclear magnetic resonance isotope shifts and 13C-2H couplings for signal assignments and determination of deuteration site in cyclooctanone",
volume = "17",
number = "4",
pages = "299-300",
doi = "10.1002/mrc.1270170415"
}

Milosavljević, S., Jeremić, D., Mihailović, M. Lj.,& Wehrli, F. W.. (1981). Deuterium‐induced 13C nuclear magnetic resonance isotope shifts and 13C-2H couplings for signal assignments and determination of deuteration site in cyclooctanone. in Organic Magnetic Resonance
Wiley., 17(4), 299-300.
https://doi.org/10.1002/mrc.1270170415

Milosavljević S, Jeremić D, Mihailović ML, Wehrli FW. Deuterium‐induced 13C nuclear magnetic resonance isotope shifts and 13C-2H couplings for signal assignments and determination of deuteration site in cyclooctanone. in Organic Magnetic Resonance. 1981;17(4):299-300.
doi:10.1002/mrc.1270170415 .

Milosavljević, Slobodan, Jeremić, Dragoslav, Mihailović, Milhailo Lj., Wehrli, Felix W., "Deuterium‐induced 13C nuclear magnetic resonance isotope shifts and 13C-2H couplings for signal assignments and determination of deuteration site in cyclooctanone" in Organic Magnetic Resonance, 17, no. 4 (1981):299-300,
https://doi.org/10.1002/mrc.1270170415 . .

TY  - JOUR
AU  - Došen-Mićović, Ljiljana
AU  - Jeremić, Dragoslav
AU  - Allinger, Norman L.
PY  - 1981
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4423
AB  - Two of the stereoisomers of the title compound were prepared and their dipole moments were measured. For the r-1,c-3-dichloro-t-5-methylcyclohexane, the free energy difference between conformers with axial-axial (aa) and equatorial-equatorial (ee) chlorines was measured by a variable temperature NMR method, and the value found was 1.3 ± 0.2 Kcal/mol-1 (in acetone) favoring the latter. Molecular mechanics studies show that the solvation energy and the electrostatics are of major importance in understanding this equilibrium. Calculations show the effect of the methyl group is essentially additive, and give for cis-1,3-dichlorocyclohexane itself ee{measured angle}aa DH+ 3.0 kcal mol-1 (acetone).
PB  - Elsevier
T2  - Tetrahedron
T1  - The conformational equilibrium of 1,3-dichloro-5-methylcyclohexane
VL  - 37
IS  - 20
SP  - 3455
EP  - 3461
DO  - 10.1016/S0040-4020(01)98859-3
ER  - 

@article{
author = "Došen-Mićović, Ljiljana and Jeremić, Dragoslav and Allinger, Norman L.",
year = "1981",
abstract = "Two of the stereoisomers of the title compound were prepared and their dipole moments were measured. For the r-1,c-3-dichloro-t-5-methylcyclohexane, the free energy difference between conformers with axial-axial (aa) and equatorial-equatorial (ee) chlorines was measured by a variable temperature NMR method, and the value found was 1.3 ± 0.2 Kcal/mol-1 (in acetone) favoring the latter. Molecular mechanics studies show that the solvation energy and the electrostatics are of major importance in understanding this equilibrium. Calculations show the effect of the methyl group is essentially additive, and give for cis-1,3-dichlorocyclohexane itself ee{measured angle}aa DH+ 3.0 kcal mol-1 (acetone).",
publisher = "Elsevier",
journal = "Tetrahedron",
title = "The conformational equilibrium of 1,3-dichloro-5-methylcyclohexane",
volume = "37",
number = "20",
pages = "3455-3461",
doi = "10.1016/S0040-4020(01)98859-3"
}

Došen-Mićović, L., Jeremić, D.,& Allinger, N. L.. (1981). The conformational equilibrium of 1,3-dichloro-5-methylcyclohexane. in Tetrahedron
Elsevier., 37(20), 3455-3461.
https://doi.org/10.1016/S0040-4020(01)98859-3

Došen-Mićović L, Jeremić D, Allinger NL. The conformational equilibrium of 1,3-dichloro-5-methylcyclohexane. in Tetrahedron. 1981;37(20):3455-3461.
doi:10.1016/S0040-4020(01)98859-3 .

Došen-Mićović, Ljiljana, Jeremić, Dragoslav, Allinger, Norman L., "The conformational equilibrium of 1,3-dichloro-5-methylcyclohexane" in Tetrahedron, 37, no. 20 (1981):3455-3461,
https://doi.org/10.1016/S0040-4020(01)98859-3 . .

TY  - JOUR
AU  - Mihailović, Milhailo Lj.
AU  - Milosavljević, Slobodan
AU  - Jeremić, Dragoslav
AU  - Milovanović, Jovan N.
PY  - 1977
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4549
AB  - The configurational and conformational relationship at C‐2 and C‐α in the two racemic diastereomeric endo‐α‐methyl‐5‐norbornene‐2‐methanols and the corresponding saturated endo‐α‐methyl‐2‐norbornanemethanols were determined by first‐order analysis of the 1H n.m.r. spectra of these compounds and of their cyclization ether products, i.e. 3‐methyl‐2‐oxatricyclo[4.2.1.04,8]nonanes and 5‐methyl‐4‐oxatricyclo[4.3.0.03,8]nonanes. In addition, the conformational preference of the hydroxyl group in the unsaturated and saturated alcohols was confirmed by the lanthanide induced shift technique, using Eu(fod)3 as shift reagent, combined with a computer program involving various conformations of the –CHOHMe group.
PB  - Wiley
T2  - Organic Magnetic Resonance
T1  - 1H n.m.r. spectra of some bicyclic compounds: I—relative configurations of the diastereomeric endo‐α‐methyl‐5‐norbornene‐2‐methanols, the corresponding saturated analogues, and their cyclization ether products
VL  - 9
IS  - 4
SP  - 229
EP  - 234
DO  - 10.1002/mrc.1270090411
ER  - 

@article{
author = "Mihailović, Milhailo Lj. and Milosavljević, Slobodan and Jeremić, Dragoslav and Milovanović, Jovan N.",
year = "1977",
abstract = "The configurational and conformational relationship at C‐2 and C‐α in the two racemic diastereomeric endo‐α‐methyl‐5‐norbornene‐2‐methanols and the corresponding saturated endo‐α‐methyl‐2‐norbornanemethanols were determined by first‐order analysis of the 1H n.m.r. spectra of these compounds and of their cyclization ether products, i.e. 3‐methyl‐2‐oxatricyclo[4.2.1.04,8]nonanes and 5‐methyl‐4‐oxatricyclo[4.3.0.03,8]nonanes. In addition, the conformational preference of the hydroxyl group in the unsaturated and saturated alcohols was confirmed by the lanthanide induced shift technique, using Eu(fod)3 as shift reagent, combined with a computer program involving various conformations of the –CHOHMe group.",
publisher = "Wiley",
journal = "Organic Magnetic Resonance",
title = "1H n.m.r. spectra of some bicyclic compounds: I—relative configurations of the diastereomeric endo‐α‐methyl‐5‐norbornene‐2‐methanols, the corresponding saturated analogues, and their cyclization ether products",
volume = "9",
number = "4",
pages = "229-234",
doi = "10.1002/mrc.1270090411"
}

Mihailović, M. Lj., Milosavljević, S., Jeremić, D.,& Milovanović, J. N.. (1977). 1H n.m.r. spectra of some bicyclic compounds: I—relative configurations of the diastereomeric endo‐α‐methyl‐5‐norbornene‐2‐methanols, the corresponding saturated analogues, and their cyclization ether products. in Organic Magnetic Resonance
Wiley., 9(4), 229-234.
https://doi.org/10.1002/mrc.1270090411

Mihailović ML, Milosavljević S, Jeremić D, Milovanović JN. 1H n.m.r. spectra of some bicyclic compounds: I—relative configurations of the diastereomeric endo‐α‐methyl‐5‐norbornene‐2‐methanols, the corresponding saturated analogues, and their cyclization ether products. in Organic Magnetic Resonance. 1977;9(4):229-234.
doi:10.1002/mrc.1270090411 .

Mihailović, Milhailo Lj., Milosavljević, Slobodan, Jeremić, Dragoslav, Milovanović, Jovan N., "1H n.m.r. spectra of some bicyclic compounds: I—relative configurations of the diastereomeric endo‐α‐methyl‐5‐norbornene‐2‐methanols, the corresponding saturated analogues, and their cyclization ether products" in Organic Magnetic Resonance, 9, no. 4 (1977):229-234,
https://doi.org/10.1002/mrc.1270090411 . .

TY  - JOUR
AU  - Jeremić, Dragoslav
AU  - Jokić, Aleksandar M.
AU  - Behbud, A.
AU  - Stefanović, Milutin
PY  - 1973
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4207
AB  - The structure of a new sesquiterpene lactone, arteannuin B, isolated from Artemisia annua L. is reported.
PB  - Elsevier
T2  - Tetrahedron Letters
T1  - A new type of sesqiterpene lactone isolated from artemisia annua L. arteannuin B
VL  - 14
IS  - 32
SP  - 3039
EP  - 3042
DO  - 10.1016/S0040-4039(01)96314-2
ER  - 

@article{
author = "Jeremić, Dragoslav and Jokić, Aleksandar M. and Behbud, A. and Stefanović, Milutin",
year = "1973",
abstract = "The structure of a new sesquiterpene lactone, arteannuin B, isolated from Artemisia annua L. is reported.",
publisher = "Elsevier",
journal = "Tetrahedron Letters",
title = "A new type of sesqiterpene lactone isolated from artemisia annua L. arteannuin B",
volume = "14",
number = "32",
pages = "3039-3042",
doi = "10.1016/S0040-4039(01)96314-2"
}

Jeremić, D., Jokić, A. M., Behbud, A.,& Stefanović, M.. (1973). A new type of sesqiterpene lactone isolated from artemisia annua L. arteannuin B. in Tetrahedron Letters
Elsevier., 14(32), 3039-3042.
https://doi.org/10.1016/S0040-4039(01)96314-2

Jeremić D, Jokić AM, Behbud A, Stefanović M. A new type of sesqiterpene lactone isolated from artemisia annua L. arteannuin B. in Tetrahedron Letters. 1973;14(32):3039-3042.
doi:10.1016/S0040-4039(01)96314-2 .

Jeremić, Dragoslav, Jokić, Aleksandar M., Behbud, A., Stefanović, Milutin, "A new type of sesqiterpene lactone isolated from artemisia annua L. arteannuin B" in Tetrahedron Letters, 14, no. 32 (1973):3039-3042,
https://doi.org/10.1016/S0040-4039(01)96314-2 . .

TY  - JOUR
AU  - Stefanović, Milutin
AU  - Mićović, Ivan V.
AU  - Jeremić, Dragoslav
AU  - Miljković, Dušan
PY  - 1970
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4593
AB  - Intramolecular cyclization by catalytic hydrogenation of 3β-acetoxy-16-picolinylidene-5-androsten-17-one (IV) (80° and 50-60 atm of hydrogen pressure over Pd/C as catalyst) gives rise to the formation of two cyclic products, namely, 5′,6′,7′,8′-tetrahydro-2′αH-3′αH-9′αH-3β-acetoxy-androst-5-eno [16.17-b]indolizine (VII) and its 9′βH-isomer (VIII), in a total yield of over 80%, the ratio of the two isomers being 3:1. The cyclized products have structures similar to naturally occuring alkaloid solanidine. A mechanism is proposed for the cyclization.
PB  - Elsevier
T2  - Tetrahedron
T1  - Intramolecular cyclization of 3β-acetoxy-16-picolinylidene-5-androsten-17-one by catalytic hydrogenation
VL  - 26
IS  - 11
SP  - 2609
EP  - 2617
DO  - 10.1016/S0040-4020(01)92835-2
ER  - 

@article{
author = "Stefanović, Milutin and Mićović, Ivan V. and Jeremić, Dragoslav and Miljković, Dušan",
year = "1970",
abstract = "Intramolecular cyclization by catalytic hydrogenation of 3β-acetoxy-16-picolinylidene-5-androsten-17-one (IV) (80° and 50-60 atm of hydrogen pressure over Pd/C as catalyst) gives rise to the formation of two cyclic products, namely, 5′,6′,7′,8′-tetrahydro-2′αH-3′αH-9′αH-3β-acetoxy-androst-5-eno [16.17-b]indolizine (VII) and its 9′βH-isomer (VIII), in a total yield of over 80%, the ratio of the two isomers being 3:1. The cyclized products have structures similar to naturally occuring alkaloid solanidine. A mechanism is proposed for the cyclization.",
publisher = "Elsevier",
journal = "Tetrahedron",
title = "Intramolecular cyclization of 3β-acetoxy-16-picolinylidene-5-androsten-17-one by catalytic hydrogenation",
volume = "26",
number = "11",
pages = "2609-2617",
doi = "10.1016/S0040-4020(01)92835-2"
}

Stefanović, M., Mićović, I. V., Jeremić, D.,& Miljković, D.. (1970). Intramolecular cyclization of 3β-acetoxy-16-picolinylidene-5-androsten-17-one by catalytic hydrogenation. in Tetrahedron
Elsevier., 26(11), 2609-2617.
https://doi.org/10.1016/S0040-4020(01)92835-2

Stefanović M, Mićović IV, Jeremić D, Miljković D. Intramolecular cyclization of 3β-acetoxy-16-picolinylidene-5-androsten-17-one by catalytic hydrogenation. in Tetrahedron. 1970;26(11):2609-2617.
doi:10.1016/S0040-4020(01)92835-2 .

Stefanović, Milutin, Mićović, Ivan V., Jeremić, Dragoslav, Miljković, Dušan, "Intramolecular cyclization of 3β-acetoxy-16-picolinylidene-5-androsten-17-one by catalytic hydrogenation" in Tetrahedron, 26, no. 11 (1970):2609-2617,
https://doi.org/10.1016/S0040-4020(01)92835-2 . .

TY  - JOUR
AU  - Mićović, Vukić M.
AU  - Stojčić, S.
AU  - Bralović, M.
AU  - Mladenović, Slobodan
AU  - Jeremić, Dragoslav
AU  - Stefanović, Milutin
PY  - 1969
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4586
AB  - Unbranched α,ω-diols are mainly converted by means of lead tetra-acetate in refluxing benzene to the corresponding ethers of di-α-tetrahydrofuryl, di-α-tetrahydropyryl and/or α-tetrahydrofuryl-α′-tetrahydropyryl type. Thus, 1,6-hexanediol affords cis-1,4-dioxaperhydropentalene (Ia) in 15·2% yield; 1,7-heptanediol affords 1,6-dioxaspiro[4.4]nonane (II) in 29·2% yield; 1,8-octanediol cyclizes to 1,6-dioxaspiro[4.5]decane (IIIa) in 39·3% yield; 1,9-nonanediol affords a mixture of di-α-tetrahydrofurylmethane (IV, 33·2%), 2-(α-tetrahydrofuryl)α′-tetrahydropyran (IVa, 3·7%) and 1,7-di-oxaspiro[5.5]undecane (IVb, 3·3%); 1,10-decanediol is oxidized to a mixture of 1,2-di-α-tetrahydrofurylethane (V, 27·2%), and threo- and erythro-α-tetrahydrofuryl-α′-tetrahydropyrylmethanes (Va, 4·3%); and 1,11-undecanediol affords, as main product, 1,3-di-α-tetrahydrofurylpropane (VI) in 40·1% yield, together with small amounts of four other ethers which were not identified.
PB  - Elsevier
T2  - Tetrahedron
T1  - The reaction of lead tetra-acetate with some unbranched α,ω-diols
VL  - 25
IS  - 5
SP  - 985
EP  - 993
DO  - 10.1016/S0040-4020(01)82671-5
ER  - 

@article{
author = "Mićović, Vukić M. and Stojčić, S. and Bralović, M. and Mladenović, Slobodan and Jeremić, Dragoslav and Stefanović, Milutin",
year = "1969",
abstract = "Unbranched α,ω-diols are mainly converted by means of lead tetra-acetate in refluxing benzene to the corresponding ethers of di-α-tetrahydrofuryl, di-α-tetrahydropyryl and/or α-tetrahydrofuryl-α′-tetrahydropyryl type. Thus, 1,6-hexanediol affords cis-1,4-dioxaperhydropentalene (Ia) in 15·2% yield; 1,7-heptanediol affords 1,6-dioxaspiro[4.4]nonane (II) in 29·2% yield; 1,8-octanediol cyclizes to 1,6-dioxaspiro[4.5]decane (IIIa) in 39·3% yield; 1,9-nonanediol affords a mixture of di-α-tetrahydrofurylmethane (IV, 33·2%), 2-(α-tetrahydrofuryl)α′-tetrahydropyran (IVa, 3·7%) and 1,7-di-oxaspiro[5.5]undecane (IVb, 3·3%); 1,10-decanediol is oxidized to a mixture of 1,2-di-α-tetrahydrofurylethane (V, 27·2%), and threo- and erythro-α-tetrahydrofuryl-α′-tetrahydropyrylmethanes (Va, 4·3%); and 1,11-undecanediol affords, as main product, 1,3-di-α-tetrahydrofurylpropane (VI) in 40·1% yield, together with small amounts of four other ethers which were not identified.",
publisher = "Elsevier",
journal = "Tetrahedron",
title = "The reaction of lead tetra-acetate with some unbranched α,ω-diols",
volume = "25",
number = "5",
pages = "985-993",
doi = "10.1016/S0040-4020(01)82671-5"
}

Mićović, V. M., Stojčić, S., Bralović, M., Mladenović, S., Jeremić, D.,& Stefanović, M.. (1969). The reaction of lead tetra-acetate with some unbranched α,ω-diols. in Tetrahedron
Elsevier., 25(5), 985-993.
https://doi.org/10.1016/S0040-4020(01)82671-5

Mićović VM, Stojčić S, Bralović M, Mladenović S, Jeremić D, Stefanović M. The reaction of lead tetra-acetate with some unbranched α,ω-diols. in Tetrahedron. 1969;25(5):985-993.
doi:10.1016/S0040-4020(01)82671-5 .

Mićović, Vukić M., Stojčić, S., Bralović, M., Mladenović, Slobodan, Jeremić, Dragoslav, Stefanović, Milutin, "The reaction of lead tetra-acetate with some unbranched α,ω-diols" in Tetrahedron, 25, no. 5 (1969):985-993,
https://doi.org/10.1016/S0040-4020(01)82671-5 . .

TY  - JOUR
AU  - Mihailović, Milhailo Lj.
AU  - Maksimović, Z.
AU  - Jeremić, Dragoslav
AU  - Čeković, Živorad M.
AU  - Milovanović, Aleksandar Ž.
AU  - Lorenc, Ljubinka B.
PY  - 1965
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4542
AB  - The action of lead tetraacetate on ethanol, 1-propanol, 2-propanol and 2-butanol has been studied under various experimental conditions, and it was found that the tetravalent lead compound reacts with alcohols in ways not so far observed. The possible reaction schemes are discussed in terms of homolytic and heterolytic cleavage of the intermediate alkoxy lead acetate complexes.
PB  - Elsevier
T2  - Tetrahedron
T1  - Reactions with lead tetraacetate-IV. Oxidation of saturated aliphatic alcohols-II; Alcohols of low molecular weight
VL  - 21
IS  - 6
SP  - 1395
EP  - 1410
DO  - 10.1016/S0040-4020(01)98301-2
ER  - 

@article{
author = "Mihailović, Milhailo Lj. and Maksimović, Z. and Jeremić, Dragoslav and Čeković, Živorad M. and Milovanović, Aleksandar Ž. and Lorenc, Ljubinka B.",
year = "1965",
abstract = "The action of lead tetraacetate on ethanol, 1-propanol, 2-propanol and 2-butanol has been studied under various experimental conditions, and it was found that the tetravalent lead compound reacts with alcohols in ways not so far observed. The possible reaction schemes are discussed in terms of homolytic and heterolytic cleavage of the intermediate alkoxy lead acetate complexes.",
publisher = "Elsevier",
journal = "Tetrahedron",
title = "Reactions with lead tetraacetate-IV. Oxidation of saturated aliphatic alcohols-II; Alcohols of low molecular weight",
volume = "21",
number = "6",
pages = "1395-1410",
doi = "10.1016/S0040-4020(01)98301-2"
}

Mihailović, M. Lj., Maksimović, Z., Jeremić, D., Čeković, Ž. M., Milovanović, A. Ž.,& Lorenc, L. B.. (1965). Reactions with lead tetraacetate-IV. Oxidation of saturated aliphatic alcohols-II; Alcohols of low molecular weight. in Tetrahedron
Elsevier., 21(6), 1395-1410.
https://doi.org/10.1016/S0040-4020(01)98301-2

Mihailović ML, Maksimović Z, Jeremić D, Čeković ŽM, Milovanović AŽ, Lorenc LB. Reactions with lead tetraacetate-IV. Oxidation of saturated aliphatic alcohols-II; Alcohols of low molecular weight. in Tetrahedron. 1965;21(6):1395-1410.
doi:10.1016/S0040-4020(01)98301-2 .

Mihailović, Milhailo Lj., Maksimović, Z., Jeremić, Dragoslav, Čeković, Živorad M., Milovanović, Aleksandar Ž., Lorenc, Ljubinka B., "Reactions with lead tetraacetate-IV. Oxidation of saturated aliphatic alcohols-II; Alcohols of low molecular weight" in Tetrahedron, 21, no. 6 (1965):1395-1410,
https://doi.org/10.1016/S0040-4020(01)98301-2 . .

TY  - JOUR
AU  - Mihailović, Milhailo Lj.
AU  - Čeković, Živorad M.
AU  - Maksimović, Z.
AU  - Jeremić, Dragoslav
AU  - Lorenc, Ljubinka B.
AU  - Mamuzić, R. I.
PY  - 1965
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4553
AB  - The action of lead tetraacetate, in benzene solution, on various unbranched primary and secondary aliphatic alcohols containing 4 to 12 carbon atoms has been investigated and the ratio of carbonyl compounds, cyclic ethers and fragmentation products determined. The results obtained are discussed with regard to the number and length of the n-alkyl rests attached to the carbinol carbon atom of the starting alcohol.
PB  - Elsevier
T2  - Tetrahedron
T1  - Lead tetraacetate oxidation of saturated aliphatic alcohols.-III. Unbranched primary and secondary alcohols
VL  - 21
IS  - 10
SP  - 2799
EP  - 2812
DO  - 10.1016/S0040-4020(01)98365-6
ER  - 

@article{
author = "Mihailović, Milhailo Lj. and Čeković, Živorad M. and Maksimović, Z. and Jeremić, Dragoslav and Lorenc, Ljubinka B. and Mamuzić, R. I.",
year = "1965",
abstract = "The action of lead tetraacetate, in benzene solution, on various unbranched primary and secondary aliphatic alcohols containing 4 to 12 carbon atoms has been investigated and the ratio of carbonyl compounds, cyclic ethers and fragmentation products determined. The results obtained are discussed with regard to the number and length of the n-alkyl rests attached to the carbinol carbon atom of the starting alcohol.",
publisher = "Elsevier",
journal = "Tetrahedron",
title = "Lead tetraacetate oxidation of saturated aliphatic alcohols.-III. Unbranched primary and secondary alcohols",
volume = "21",
number = "10",
pages = "2799-2812",
doi = "10.1016/S0040-4020(01)98365-6"
}

Mihailović, M. Lj., Čeković, Ž. M., Maksimović, Z., Jeremić, D., Lorenc, L. B.,& Mamuzić, R. I.. (1965). Lead tetraacetate oxidation of saturated aliphatic alcohols.-III. Unbranched primary and secondary alcohols. in Tetrahedron
Elsevier., 21(10), 2799-2812.
https://doi.org/10.1016/S0040-4020(01)98365-6

Mihailović ML, Čeković ŽM, Maksimović Z, Jeremić D, Lorenc LB, Mamuzić RI. Lead tetraacetate oxidation of saturated aliphatic alcohols.-III. Unbranched primary and secondary alcohols. in Tetrahedron. 1965;21(10):2799-2812.
doi:10.1016/S0040-4020(01)98365-6 .

Mihailović, Milhailo Lj., Čeković, Živorad M., Maksimović, Z., Jeremić, Dragoslav, Lorenc, Ljubinka B., Mamuzić, R. I., "Lead tetraacetate oxidation of saturated aliphatic alcohols.-III. Unbranched primary and secondary alcohols" in Tetrahedron, 21, no. 10 (1965):2799-2812,
https://doi.org/10.1016/S0040-4020(01)98365-6 . .

TY  - JOUR
AU  - Mihailović, Milhailo Lj.
AU  - Čeković, Živorad M.
AU  - Jeremić, Dragoslav
PY  - 1965
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4628
AB  - The lead tetraacetate oxidation of saturated aliphatic alcohols, with structures which do not permit 1,5-cyclization, gave tetrahydropyran derivatives in yields not exceeding 16%. The formation of a small amount of the rearranged ether, 2-ethyl-2-methyltetrahydrofuran, from 4,4-dimethyl-1-pentanol indicates that the cyclization reaction proceeds via an intermediate with carbonium ion character.
PB  - Elsevier
T2  - Tetrahedron
T1  - Lead tetraacetate oxidation of saturated aliphatic alcohols-IV. The formation of six-membered cyclic ethers
VL  - 21
IS  - 10
SP  - 2813
EP  - 2821
DO  - 10.1016/S0040-4020(01)98366-8
ER  - 

@article{
author = "Mihailović, Milhailo Lj. and Čeković, Živorad M. and Jeremić, Dragoslav",
year = "1965",
abstract = "The lead tetraacetate oxidation of saturated aliphatic alcohols, with structures which do not permit 1,5-cyclization, gave tetrahydropyran derivatives in yields not exceeding 16%. The formation of a small amount of the rearranged ether, 2-ethyl-2-methyltetrahydrofuran, from 4,4-dimethyl-1-pentanol indicates that the cyclization reaction proceeds via an intermediate with carbonium ion character.",
publisher = "Elsevier",
journal = "Tetrahedron",
title = "Lead tetraacetate oxidation of saturated aliphatic alcohols-IV. The formation of six-membered cyclic ethers",
volume = "21",
number = "10",
pages = "2813-2821",
doi = "10.1016/S0040-4020(01)98366-8"
}

Mihailović, M. Lj., Čeković, Ž. M.,& Jeremić, D.. (1965). Lead tetraacetate oxidation of saturated aliphatic alcohols-IV. The formation of six-membered cyclic ethers. in Tetrahedron
Elsevier., 21(10), 2813-2821.
https://doi.org/10.1016/S0040-4020(01)98366-8

Mihailović ML, Čeković ŽM, Jeremić D. Lead tetraacetate oxidation of saturated aliphatic alcohols-IV. The formation of six-membered cyclic ethers. in Tetrahedron. 1965;21(10):2813-2821.
doi:10.1016/S0040-4020(01)98366-8 .

Mihailović, Milhailo Lj., Čeković, Živorad M., Jeremić, Dragoslav, "Lead tetraacetate oxidation of saturated aliphatic alcohols-IV. The formation of six-membered cyclic ethers" in Tetrahedron, 21, no. 10 (1965):2813-2821,
https://doi.org/10.1016/S0040-4020(01)98366-8 . .

TY  - JOUR
AU  - Mićović, Vukić M.
AU  - Mamuzić, R. I.
AU  - Jeremić, Dragoslav
AU  - Mihailović, Milhailo Lj.
PY  - 1964
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4627
AB  - When oxidized with lead tetraacetate 1-heptanol and 1-octanol undergo cyclization to give as major products the corresponding 2-alkyltetrahydrofurans, accompanied by a small amount of the isomeric tetrahydropyran derivatives. Secondary aliphatic alcohols, under similar conditions, are converted to a mixture of cis and trans 2,5-dialkyltetrahydrofurans.
PB  - Elsevier
T2  - Tetrahedron
T1  - Reactions with lead tetraacetate-I. Oxidation of saturated aliphatic alcohols part 1
VL  - 20
IS  - 10
SP  - 2279
EP  - 2287
DO  - 10.1016/S0040-4020(01)97615-X
ER  - 

@article{
author = "Mićović, Vukić M. and Mamuzić, R. I. and Jeremić, Dragoslav and Mihailović, Milhailo Lj.",
year = "1964",
abstract = "When oxidized with lead tetraacetate 1-heptanol and 1-octanol undergo cyclization to give as major products the corresponding 2-alkyltetrahydrofurans, accompanied by a small amount of the isomeric tetrahydropyran derivatives. Secondary aliphatic alcohols, under similar conditions, are converted to a mixture of cis and trans 2,5-dialkyltetrahydrofurans.",
publisher = "Elsevier",
journal = "Tetrahedron",
title = "Reactions with lead tetraacetate-I. Oxidation of saturated aliphatic alcohols part 1",
volume = "20",
number = "10",
pages = "2279-2287",
doi = "10.1016/S0040-4020(01)97615-X"
}

Mićović, V. M., Mamuzić, R. I., Jeremić, D.,& Mihailović, M. Lj.. (1964). Reactions with lead tetraacetate-I. Oxidation of saturated aliphatic alcohols part 1. in Tetrahedron
Elsevier., 20(10), 2279-2287.
https://doi.org/10.1016/S0040-4020(01)97615-X

Mićović VM, Mamuzić RI, Jeremić D, Mihailović ML. Reactions with lead tetraacetate-I. Oxidation of saturated aliphatic alcohols part 1. in Tetrahedron. 1964;20(10):2279-2287.
doi:10.1016/S0040-4020(01)97615-X .

Mićović, Vukić M., Mamuzić, R. I., Jeremić, Dragoslav, Mihailović, Milhailo Lj., "Reactions with lead tetraacetate-I. Oxidation of saturated aliphatic alcohols part 1" in Tetrahedron, 20, no. 10 (1964):2279-2287,
https://doi.org/10.1016/S0040-4020(01)97615-X . .

TY  - JOUR
AU  - Mićović, Vukić M.
AU  - Mamuzić, R. I.
AU  - Jeremić, Dragoslav
AU  - Mihailović, Milhailo Lj.
PY  - 1963
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4657
AB  - It was recently shown that various steroid alcohols could react with lead tetraacetate in non-polar solvents to give tetrahydrofuran and tetrahydropyran derivatives. cyclization occurring when the position of and the distance between the reacting hydroxyl group and the 8 - or d -methyl, methylene or methine group were favourable to ring closure.
PB  - Elsevier
T2  - Tetrahedron Letters
T1  - Reactions with lead tetraacetate. I. Oxidation of saturated aliphatic alcohols. Part 1
VL  - 4
IS  - 29
SP  - 2091
EP  - 2095
DO  - 10.1016/S0040-4039(01)90975-X
ER  - 

@article{
author = "Mićović, Vukić M. and Mamuzić, R. I. and Jeremić, Dragoslav and Mihailović, Milhailo Lj.",
year = "1963",
abstract = "It was recently shown that various steroid alcohols could react with lead tetraacetate in non-polar solvents to give tetrahydrofuran and tetrahydropyran derivatives. cyclization occurring when the position of and the distance between the reacting hydroxyl group and the 8 - or d -methyl, methylene or methine group were favourable to ring closure.",
publisher = "Elsevier",
journal = "Tetrahedron Letters",
title = "Reactions with lead tetraacetate. I. Oxidation of saturated aliphatic alcohols. Part 1",
volume = "4",
number = "29",
pages = "2091-2095",
doi = "10.1016/S0040-4039(01)90975-X"
}

Mićović, V. M., Mamuzić, R. I., Jeremić, D.,& Mihailović, M. Lj.. (1963). Reactions with lead tetraacetate. I. Oxidation of saturated aliphatic alcohols. Part 1. in Tetrahedron Letters
Elsevier., 4(29), 2091-2095.
https://doi.org/10.1016/S0040-4039(01)90975-X

Mićović VM, Mamuzić RI, Jeremić D, Mihailović ML. Reactions with lead tetraacetate. I. Oxidation of saturated aliphatic alcohols. Part 1. in Tetrahedron Letters. 1963;4(29):2091-2095.
doi:10.1016/S0040-4039(01)90975-X .

Mićović, Vukić M., Mamuzić, R. I., Jeremić, Dragoslav, Mihailović, Milhailo Lj., "Reactions with lead tetraacetate. I. Oxidation of saturated aliphatic alcohols. Part 1" in Tetrahedron Letters, 4, no. 29 (1963):2091-2095,
https://doi.org/10.1016/S0040-4039(01)90975-X . .