TY  - DATA
AU  - Marković, Rade
AU  - Rašović, Aleksandar
AU  - Steel, Peter
PY  - 2008
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4592
AB  - GISGAR : Ethyl 3-(6-phenyl-4λ4[1,2]dithiolo[1,5-b][1,2,4]dithiazol-2-yl)propanoate Space Group: P 21/c (14), Cell: a 4.5830(8)Å b 15.550(3)Å c 21.858(4)Å, α 90° β 91.579(2)° γ 90°
PB  - The Cambridge Crystallographic Data Centre (CCDC)
T1  - CCDC 271489: Experimental Crystal Structure Determination. Crystallographic data for "Ethyl 3-(6-phenyl-44-1,2-dithiolo[1,5-b][1,2,4]dithiazol-2-yl) propanoate, Acta Crystallographica Section E: Structure Reports Online, 2008, 64, 1"
DO  - 10.5517/cc93hql
ER  - 

@misc{
author = "Marković, Rade and Rašović, Aleksandar and Steel, Peter",
year = "2008",
abstract = "GISGAR : Ethyl 3-(6-phenyl-4λ4[1,2]dithiolo[1,5-b][1,2,4]dithiazol-2-yl)propanoate Space Group: P 21/c (14), Cell: a 4.5830(8)Å b 15.550(3)Å c 21.858(4)Å, α 90° β 91.579(2)° γ 90°",
publisher = "The Cambridge Crystallographic Data Centre (CCDC)",
title = "CCDC 271489: Experimental Crystal Structure Determination. Crystallographic data for "Ethyl 3-(6-phenyl-44-1,2-dithiolo[1,5-b][1,2,4]dithiazol-2-yl) propanoate, Acta Crystallographica Section E: Structure Reports Online, 2008, 64, 1"",
doi = "10.5517/cc93hql"
}

Marković, R., Rašović, A.,& Steel, P.. (2008). CCDC 271489: Experimental Crystal Structure Determination. Crystallographic data for "Ethyl 3-(6-phenyl-44-1,2-dithiolo[1,5-b][1,2,4]dithiazol-2-yl) propanoate, Acta Crystallographica Section E: Structure Reports Online, 2008, 64, 1". 
The Cambridge Crystallographic Data Centre (CCDC)..
https://doi.org/10.5517/cc93hql

Marković R, Rašović A, Steel P. CCDC 271489: Experimental Crystal Structure Determination. Crystallographic data for "Ethyl 3-(6-phenyl-44-1,2-dithiolo[1,5-b][1,2,4]dithiazol-2-yl) propanoate, Acta Crystallographica Section E: Structure Reports Online, 2008, 64, 1". 2008;.
doi:10.5517/cc93hql .

Marković, Rade, Rašović, Aleksandar, Steel, Peter, "CCDC 271489: Experimental Crystal Structure Determination. Crystallographic data for "Ethyl 3-(6-phenyl-44-1,2-dithiolo[1,5-b][1,2,4]dithiazol-2-yl) propanoate, Acta Crystallographica Section E: Structure Reports Online, 2008, 64, 1"" (2008),
https://doi.org/10.5517/cc93hql . .

TY  - JOUR
AU  - Marković, Rade
AU  - Rašović, Aleksandar
AU  - Steel, Peter
PY  - 2008
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/470
AB  - The title compound, C15H15NO2S3, exists in a bicyclic form, with resonance contributions from two monocyclic forms, each without a second S - S bond. The trithiapentalene heterocyclic ring system is planar, with a mean deviation of 0.014 (2) Å from the mean plane, and is inclined to the plane of the attached phenyl ring at an angle of 17.24 (7)°.
PB  - International Union of Crystallography
T2  - Acta Crystallographica Section E: Structure Reports Online
T1  - Ethyl 3-(6-phenyl-44-1,2-dithiolo[1,5-b][1,2,4]dithiazol-2-yl) propanoate
VL  - 64
IS  - 1
DO  - 10.1107/S1600536807063209
ER  - 

@article{
author = "Marković, Rade and Rašović, Aleksandar and Steel, Peter",
year = "2008",
abstract = "The title compound, C15H15NO2S3, exists in a bicyclic form, with resonance contributions from two monocyclic forms, each without a second S - S bond. The trithiapentalene heterocyclic ring system is planar, with a mean deviation of 0.014 (2) Å from the mean plane, and is inclined to the plane of the attached phenyl ring at an angle of 17.24 (7)°.",
publisher = "International Union of Crystallography",
journal = "Acta Crystallographica Section E: Structure Reports Online",
title = "Ethyl 3-(6-phenyl-44-1,2-dithiolo[1,5-b][1,2,4]dithiazol-2-yl) propanoate",
volume = "64",
number = "1",
doi = "10.1107/S1600536807063209"
}

Marković, R., Rašović, A.,& Steel, P.. (2008). Ethyl 3-(6-phenyl-44-1,2-dithiolo[1,5-b][1,2,4]dithiazol-2-yl) propanoate. in Acta Crystallographica Section E: Structure Reports Online
International Union of Crystallography., 64(1).
https://doi.org/10.1107/S1600536807063209

Marković R, Rašović A, Steel P. Ethyl 3-(6-phenyl-44-1,2-dithiolo[1,5-b][1,2,4]dithiazol-2-yl) propanoate. in Acta Crystallographica Section E: Structure Reports Online. 2008;64(1).
doi:10.1107/S1600536807063209 .

Marković, Rade, Rašović, Aleksandar, Steel, Peter, "Ethyl 3-(6-phenyl-44-1,2-dithiolo[1,5-b][1,2,4]dithiazol-2-yl) propanoate" in Acta Crystallographica Section E: Structure Reports Online, 64, no. 1 (2008),
https://doi.org/10.1107/S1600536807063209 . .

TY  - JOUR
AU  - Rašović, Aleksandar
AU  - Steel, Peter J.
AU  - Kleinpeter, Erich
AU  - Marković, Rade
PY  - 2007
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4255
AB  - A new synthetic approach to 2,3-dihydro-4H-1,3-thiazine derivatives based upon reductive rearrangement of 1,2-dithiole-3-ylidene thiones has been developed. In turn, the 1,2-dithiole derivatives were prepared by an efficient ring-opening-closing process of 2-alkylidene-4-oxothiazolidines, induced in the presence of Lawesson's reagent by intramolecular non-bonded 1,5-type S⋯O interactions in the 4-oxothiazolidine precursors.
PB  - Elsevier
T2  - Tetrahedron
T1  - Regioselective synthesis of 1,3-thiazines by sequential 4-oxothiazolidine to 1,2-dithiole to 1,3-thiazine transformations: role of intramolecular non-bonded S/O interactions
VL  - 63
IS  - 9
SP  - 1937
EP  - 1945
DO  - 10.1016/j.tet.2006.12.075
ER  - 

@article{
author = "Rašović, Aleksandar and Steel, Peter J. and Kleinpeter, Erich and Marković, Rade",
year = "2007",
abstract = "A new synthetic approach to 2,3-dihydro-4H-1,3-thiazine derivatives based upon reductive rearrangement of 1,2-dithiole-3-ylidene thiones has been developed. In turn, the 1,2-dithiole derivatives were prepared by an efficient ring-opening-closing process of 2-alkylidene-4-oxothiazolidines, induced in the presence of Lawesson's reagent by intramolecular non-bonded 1,5-type S⋯O interactions in the 4-oxothiazolidine precursors.",
publisher = "Elsevier",
journal = "Tetrahedron",
title = "Regioselective synthesis of 1,3-thiazines by sequential 4-oxothiazolidine to 1,2-dithiole to 1,3-thiazine transformations: role of intramolecular non-bonded S/O interactions",
volume = "63",
number = "9",
pages = "1937-1945",
doi = "10.1016/j.tet.2006.12.075"
}

Rašović, A., Steel, P. J., Kleinpeter, E.,& Marković, R.. (2007). Regioselective synthesis of 1,3-thiazines by sequential 4-oxothiazolidine to 1,2-dithiole to 1,3-thiazine transformations: role of intramolecular non-bonded S/O interactions. in Tetrahedron
Elsevier., 63(9), 1937-1945.
https://doi.org/10.1016/j.tet.2006.12.075

Rašović A, Steel PJ, Kleinpeter E, Marković R. Regioselective synthesis of 1,3-thiazines by sequential 4-oxothiazolidine to 1,2-dithiole to 1,3-thiazine transformations: role of intramolecular non-bonded S/O interactions. in Tetrahedron. 2007;63(9):1937-1945.
doi:10.1016/j.tet.2006.12.075 .

Rašović, Aleksandar, Steel, Peter J., Kleinpeter, Erich, Marković, Rade, "Regioselective synthesis of 1,3-thiazines by sequential 4-oxothiazolidine to 1,2-dithiole to 1,3-thiazine transformations: role of intramolecular non-bonded S/O interactions" in Tetrahedron, 63, no. 9 (2007):1937-1945,
https://doi.org/10.1016/j.tet.2006.12.075 . .

TY  - JOUR
AU  - Marković, Rade
AU  - Rašović, Aleksandar
AU  - Baranac, Marija M.
AU  - Stojanović, Milovan
AU  - Steel, Peter
AU  - Jovetić, Stanka L.
PY  - 2004
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/139
AB  - The potential of directional non-bonded 1,5-type S···O interactions to initiate the incipient stage of an in situ rearrangement of N-unsubstituted thiazolidine enaminones to functionalized 1,2-dithioles has been demonstrated. The spectral characteristics, as well as X-ray structural analysis of a selected rearranged product, indicate that a dynamic interconversion occurs in solution between the 1,2-dithiole and the 3,3aλ4,4-trithia-1-azapentalene bicylic form. The lack of the rearrangement in the case of a N-methyl substituted enaminone precursor is attributed to an unfavorable methyl migration in the last reaction step.
AB  - Pokazan je potencijal usmerenih nevezivnih interakcija 1,5-tipa S···O da iniciraju početnu fazu in situ premeštanja N-nesupstituisanih tiazolidinonskih enaminona u funkcionalizovane 1,2-ditiole. Spektralne karakteristike, kao i kristalografska strukturna analiza izabranog premeštenog proizvoda, ukazuju na brzu interkonverziju između 1,2-ditiola i 3, 3aλ4,4-tritija-1-azapentalenskog bicikličnog oblika. Odsustvo premeštanja u slučaju N-metil-supstituisanog enaminomskog prekursora pripisano je nefavorizovanom premeštanju metil-grupe u završnoj fazi reakcije.
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Thionation of N-methyl- and N-unsubstituted thiazolidine enaminones
T1  - Tionovanje n-metil- i n-nesupstituisanih tiazolidinonskih enaminona
VL  - 69
IS  - 11
SP  - 909
EP  - 918
DO  - 10.2298/JSC0411909M
ER  - 

@article{
author = "Marković, Rade and Rašović, Aleksandar and Baranac, Marija M. and Stojanović, Milovan and Steel, Peter and Jovetić, Stanka L.",
year = "2004",
abstract = "The potential of directional non-bonded 1,5-type S···O interactions to initiate the incipient stage of an in situ rearrangement of N-unsubstituted thiazolidine enaminones to functionalized 1,2-dithioles has been demonstrated. The spectral characteristics, as well as X-ray structural analysis of a selected rearranged product, indicate that a dynamic interconversion occurs in solution between the 1,2-dithiole and the 3,3aλ4,4-trithia-1-azapentalene bicylic form. The lack of the rearrangement in the case of a N-methyl substituted enaminone precursor is attributed to an unfavorable methyl migration in the last reaction step., Pokazan je potencijal usmerenih nevezivnih interakcija 1,5-tipa S···O da iniciraju početnu fazu in situ premeštanja N-nesupstituisanih tiazolidinonskih enaminona u funkcionalizovane 1,2-ditiole. Spektralne karakteristike, kao i kristalografska strukturna analiza izabranog premeštenog proizvoda, ukazuju na brzu interkonverziju između 1,2-ditiola i 3, 3aλ4,4-tritija-1-azapentalenskog bicikličnog oblika. Odsustvo premeštanja u slučaju N-metil-supstituisanog enaminomskog prekursora pripisano je nefavorizovanom premeštanju metil-grupe u završnoj fazi reakcije.",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Thionation of N-methyl- and N-unsubstituted thiazolidine enaminones, Tionovanje n-metil- i n-nesupstituisanih tiazolidinonskih enaminona",
volume = "69",
number = "11",
pages = "909-918",
doi = "10.2298/JSC0411909M"
}

Marković, R., Rašović, A., Baranac, M. M., Stojanović, M., Steel, P.,& Jovetić, S. L.. (2004). Thionation of N-methyl- and N-unsubstituted thiazolidine enaminones. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 69(11), 909-918.
https://doi.org/10.2298/JSC0411909M

Marković R, Rašović A, Baranac MM, Stojanović M, Steel P, Jovetić SL. Thionation of N-methyl- and N-unsubstituted thiazolidine enaminones. in Journal of the Serbian Chemical Society. 2004;69(11):909-918.
doi:10.2298/JSC0411909M .

Marković, Rade, Rašović, Aleksandar, Baranac, Marija M., Stojanović, Milovan, Steel, Peter, Jovetić, Stanka L., "Thionation of N-methyl- and N-unsubstituted thiazolidine enaminones" in Journal of the Serbian Chemical Society, 69, no. 11 (2004):909-918,
https://doi.org/10.2298/JSC0411909M . .

TY  - JOUR
AU  - Marković, Rade
AU  - Džambaski, Zdravko
AU  - Stojanović, Milovan
AU  - Steel, Peter
AU  - Baranac, Marija M.
PY  - 2003
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/114
AB  - Astudy on the regiospecificity of the base-catalyzed reaction of activated β-oxonitriles 1 with diethyl mercaptosuccinate affording the title compounds 3 is reported. Other competitive heterocyclic products, that is 4-oxo-1,3-thiazinanes 4, derivatives of tetrahydrothiophene 5 and/or thiacyclohexane 6 which on the grounds of mechanistic considerations could be formed, were not observed. Spectroscopic and experimental evidence together with theoretical considerations, provides a reasonable explanation for the observed regiospecificity.
AB  - Proučavana je regiospecifičnost bazno-katalizovane reakcije aktiviranih β-oksonitrilado 1 sa dietil-estrom merkaptoćilibarne kiseline u kojoj se grade u naslovu navedena jedinjenja 3. Mogući heterociklični proizvodi 4-okso-1,3-tiazini 4, derivati tetrahidrotiofena 5 i/ili tijacikloheksana 6 koji mogu biti nagrađeni na osnovu mehanističkog razmatranja, nisu detektovani. Spektroskopski i eksperimentalni dokazi sa teorijskim obrazloženjem daju prihvatljivo objašnjenje za uočenu regiospecifičnost.
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Regiospecificty in the heterocyclization of β-oxonitriles to 5-substituted 4-oxothiazolidine derivatives
T1  - Regiospecifičnost u heterociklizaciji β-oksonitrilado 5-supstituisanih 4-oksotiazolidinskih derivata
VL  - 68
IS  - 4-5
SP  - 383
EP  - 390
DO  - 10.2298/JSC0305383M
ER  - 

@article{
author = "Marković, Rade and Džambaski, Zdravko and Stojanović, Milovan and Steel, Peter and Baranac, Marija M.",
year = "2003",
abstract = "Astudy on the regiospecificity of the base-catalyzed reaction of activated β-oxonitriles 1 with diethyl mercaptosuccinate affording the title compounds 3 is reported. Other competitive heterocyclic products, that is 4-oxo-1,3-thiazinanes 4, derivatives of tetrahydrothiophene 5 and/or thiacyclohexane 6 which on the grounds of mechanistic considerations could be formed, were not observed. Spectroscopic and experimental evidence together with theoretical considerations, provides a reasonable explanation for the observed regiospecificity., Proučavana je regiospecifičnost bazno-katalizovane reakcije aktiviranih β-oksonitrilado 1 sa dietil-estrom merkaptoćilibarne kiseline u kojoj se grade u naslovu navedena jedinjenja 3. Mogući heterociklični proizvodi 4-okso-1,3-tiazini 4, derivati tetrahidrotiofena 5 i/ili tijacikloheksana 6 koji mogu biti nagrađeni na osnovu mehanističkog razmatranja, nisu detektovani. Spektroskopski i eksperimentalni dokazi sa teorijskim obrazloženjem daju prihvatljivo objašnjenje za uočenu regiospecifičnost.",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Regiospecificty in the heterocyclization of β-oxonitriles to 5-substituted 4-oxothiazolidine derivatives, Regiospecifičnost u heterociklizaciji β-oksonitrilado 5-supstituisanih 4-oksotiazolidinskih derivata",
volume = "68",
number = "4-5",
pages = "383-390",
doi = "10.2298/JSC0305383M"
}

Marković, R., Džambaski, Z., Stojanović, M., Steel, P.,& Baranac, M. M.. (2003). Regiospecificty in the heterocyclization of β-oxonitriles to 5-substituted 4-oxothiazolidine derivatives. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 68(4-5), 383-390.
https://doi.org/10.2298/JSC0305383M

Marković R, Džambaski Z, Stojanović M, Steel P, Baranac MM. Regiospecificty in the heterocyclization of β-oxonitriles to 5-substituted 4-oxothiazolidine derivatives. in Journal of the Serbian Chemical Society. 2003;68(4-5):383-390.
doi:10.2298/JSC0305383M .

Marković, Rade, Džambaski, Zdravko, Stojanović, Milovan, Steel, Peter, Baranac, Marija M., "Regiospecificty in the heterocyclization of β-oxonitriles to 5-substituted 4-oxothiazolidine derivatives" in Journal of the Serbian Chemical Society, 68, no. 4-5 (2003):383-390,
https://doi.org/10.2298/JSC0305383M . .