Andrejević, Vladimir

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Authority KeyName Variants
545c114a-f0da-461b-a8cd-22936c01ce0f
  • Andrejević, Vladimir (2)
  • Andrejević Vladimir (1)
Projects

Author's Bibliography

The Reductive Conversion of Some Cyclic and Acyclic vic-Epoxides to Alcohols by Means of Lithium Aluminium Hydride/Aluminium Trichloride

Andrejević Vladimir; Bjelaković, Mira; Mihailović, Milan M.; Mihailović, Milhailo Lj.

(Wiley, 1985)

TY  - JOUR
AU  - Andrejević Vladimir
AU  - Bjelaković, Mira
AU  - Mihailović, Milan M.
AU  - Mihailović, Milhailo Lj.
PY  - 1985
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4185
AB  - Unsubstituted medium‐ring 1,2‐epoxycycloalkanes and certain vic‐epoxyalkanes are reduced to the corresponding alcohols very slowly when LiAlH4 alone is used as reducing agent. However, the combination of LiAlH4 and AlCl3, in a 2:1 molar ratio (with respect to 1 mol‐equiv. of epoxide) used in refluxing Et2O, greatly enhances these reductions, rendering them of interest for practical purposes.
PB  - Wiley
T2  - Helvetica Chimica Acta
T1  - The Reductive Conversion of Some Cyclic and Acyclic vic-Epoxides to Alcohols by Means of Lithium Aluminium Hydride/Aluminium Trichloride
VL  - 68
IS  - 7
SP  - 2030
EP  - 2032
DO  - 10.1002/hlca.19850680727
ER  - 
@article{
author = "Andrejević Vladimir and Bjelaković, Mira and Mihailović, Milan M. and Mihailović, Milhailo Lj.",
year = "1985",
abstract = "Unsubstituted medium‐ring 1,2‐epoxycycloalkanes and certain vic‐epoxyalkanes are reduced to the corresponding alcohols very slowly when LiAlH4 alone is used as reducing agent. However, the combination of LiAlH4 and AlCl3, in a 2:1 molar ratio (with respect to 1 mol‐equiv. of epoxide) used in refluxing Et2O, greatly enhances these reductions, rendering them of interest for practical purposes.",
publisher = "Wiley",
journal = "Helvetica Chimica Acta",
title = "The Reductive Conversion of Some Cyclic and Acyclic vic-Epoxides to Alcohols by Means of Lithium Aluminium Hydride/Aluminium Trichloride",
volume = "68",
number = "7",
pages = "2030-2032",
doi = "10.1002/hlca.19850680727"
}
Andrejević Vladimir, Bjelaković, M., Mihailović, M. M.,& Mihailović, M. Lj.. (1985). The Reductive Conversion of Some Cyclic and Acyclic vic-Epoxides to Alcohols by Means of Lithium Aluminium Hydride/Aluminium Trichloride. in Helvetica Chimica Acta
Wiley., 68(7), 2030-2032.
https://doi.org/10.1002/hlca.19850680727
Andrejević Vladimir, Bjelaković M, Mihailović MM, Mihailović ML. The Reductive Conversion of Some Cyclic and Acyclic vic-Epoxides to Alcohols by Means of Lithium Aluminium Hydride/Aluminium Trichloride. in Helvetica Chimica Acta. 1985;68(7):2030-2032.
doi:10.1002/hlca.19850680727 .
Andrejević Vladimir, Bjelaković, Mira, Mihailović, Milan M., Mihailović, Milhailo Lj., "The Reductive Conversion of Some Cyclic and Acyclic vic-Epoxides to Alcohols by Means of Lithium Aluminium Hydride/Aluminium Trichloride" in Helvetica Chimica Acta, 68, no. 7 (1985):2030-2032,
https://doi.org/10.1002/hlca.19850680727 . .
13
10

The Reduction of Some 1, 2‐Epoxides with Lithium Aluminium Hydride. Preliminary Communication

Mihailović, Milhailo Lj.; Andrejević, Vladimir; Milovanović, Jovan N.; Janković, Jovan

(Wiley - VCH Verlag GmbH & Co, 1976)

TY  - JOUR
AU  - Mihailović, Milhailo Lj.
AU  - Andrejević, Vladimir
AU  - Milovanović, Jovan N.
AU  - Janković, Jovan
PY  - 1976
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4712
AB  - The factors influencing the ease of the lithium aluminium hydride reduction of various 1,2‐epoxycycloalkanes and 1,2‐epoxyalkanes are described and discussed.
PB  - Wiley - VCH Verlag GmbH & Co
T2  - Helvetica Chimica Acta
T1  - The Reduction of Some 1, 2‐Epoxides with Lithium Aluminium Hydride. Preliminary Communication
VL  - 59
IS  - 7
SP  - 2305
EP  - 2307
DO  - 10.1002/hlca.19760590702
ER  - 
@article{
author = "Mihailović, Milhailo Lj. and Andrejević, Vladimir and Milovanović, Jovan N. and Janković, Jovan",
year = "1976",
abstract = "The factors influencing the ease of the lithium aluminium hydride reduction of various 1,2‐epoxycycloalkanes and 1,2‐epoxyalkanes are described and discussed.",
publisher = "Wiley - VCH Verlag GmbH & Co",
journal = "Helvetica Chimica Acta",
title = "The Reduction of Some 1, 2‐Epoxides with Lithium Aluminium Hydride. Preliminary Communication",
volume = "59",
number = "7",
pages = "2305-2307",
doi = "10.1002/hlca.19760590702"
}
Mihailović, M. Lj., Andrejević, V., Milovanović, J. N.,& Janković, J.. (1976). The Reduction of Some 1, 2‐Epoxides with Lithium Aluminium Hydride. Preliminary Communication. in Helvetica Chimica Acta
Wiley - VCH Verlag GmbH & Co., 59(7), 2305-2307.
https://doi.org/10.1002/hlca.19760590702
Mihailović ML, Andrejević V, Milovanović JN, Janković J. The Reduction of Some 1, 2‐Epoxides with Lithium Aluminium Hydride. Preliminary Communication. in Helvetica Chimica Acta. 1976;59(7):2305-2307.
doi:10.1002/hlca.19760590702 .
Mihailović, Milhailo Lj., Andrejević, Vladimir, Milovanović, Jovan N., Janković, Jovan, "The Reduction of Some 1, 2‐Epoxides with Lithium Aluminium Hydride. Preliminary Communication" in Helvetica Chimica Acta, 59, no. 7 (1976):2305-2307,
https://doi.org/10.1002/hlca.19760590702 . .
17
9

The conversion of unbranched primary alkyl and arylalkyl amines to nitriles by means of lead tetraacetate

Mihailović, Milhailo Lj.; Stojiljković, A.; Andrejević, Vladimir

(Elsevier, 1965)

TY  - JOUR
AU  - Mihailović, Milhailo Lj.
AU  - Stojiljković, A.
AU  - Andrejević, Vladimir
PY  - 1965
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4655
AB  - The only amino compounds oxidized so far with lead tetroacetate were primary aromatic amines, which gave mainly the corresponding azo compounds(1), and some tertiary aryldialkyl amines, which in glacial acetic acid in the presence of acetic acid anhydride underwent oxidative dealkylation with the formation of acetylated secondary amines (2).
PB  - Elsevier
T2  - Tetrahedron Letters
T1  - The conversion of unbranched primary alkyl and arylalkyl amines to nitriles by means of lead tetraacetate
VL  - 6
IS  - 8
SP  - 461
EP  - 464
DO  - 10.1016/S0040-4039(00)89979-7
ER  - 
@article{
author = "Mihailović, Milhailo Lj. and Stojiljković, A. and Andrejević, Vladimir",
year = "1965",
abstract = "The only amino compounds oxidized so far with lead tetroacetate were primary aromatic amines, which gave mainly the corresponding azo compounds(1), and some tertiary aryldialkyl amines, which in glacial acetic acid in the presence of acetic acid anhydride underwent oxidative dealkylation with the formation of acetylated secondary amines (2).",
publisher = "Elsevier",
journal = "Tetrahedron Letters",
title = "The conversion of unbranched primary alkyl and arylalkyl amines to nitriles by means of lead tetraacetate",
volume = "6",
number = "8",
pages = "461-464",
doi = "10.1016/S0040-4039(00)89979-7"
}
Mihailović, M. Lj., Stojiljković, A.,& Andrejević, V.. (1965). The conversion of unbranched primary alkyl and arylalkyl amines to nitriles by means of lead tetraacetate. in Tetrahedron Letters
Elsevier., 6(8), 461-464.
https://doi.org/10.1016/S0040-4039(00)89979-7
Mihailović ML, Stojiljković A, Andrejević V. The conversion of unbranched primary alkyl and arylalkyl amines to nitriles by means of lead tetraacetate. in Tetrahedron Letters. 1965;6(8):461-464.
doi:10.1016/S0040-4039(00)89979-7 .
Mihailović, Milhailo Lj., Stojiljković, A., Andrejević, Vladimir, "The conversion of unbranched primary alkyl and arylalkyl amines to nitriles by means of lead tetraacetate" in Tetrahedron Letters, 6, no. 8 (1965):461-464,
https://doi.org/10.1016/S0040-4039(00)89979-7 . .
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