endo-Mode cyclizations of vinylogous N-acyliminium ions as a route to the synthesis of condensed thiazolidines
Само за регистроване кориснике
2011
Чланак у часопису (Објављена верзија)
Метаподаци
Приказ свих података о документуАпстракт
endo-Mode cyclizations of vinylogous N-acyliminium ions incorporating heteroatom-based nucleophiles have been examined as a route to the synthesis of condensed thiazolidines. The scope of these reactions and stereochemical outcome are discussed and explained using quantum chemical calculations.
Кључне речи:
Vinylogous N-acyliminium ion / endo-Mode cyclization / Condensed thiazolidines / Quantum chemical calculationsИзвор:
Tetrahedron, 2011, 67, 49, 9541-9554Издавач:
- Oxford : Pergamon-Elsevier Science Ltd
Финансирање / пројекти:
- Тиазолидни и синтетички аналози: реактивност, примена и биолошка активност (RS-MESTD-MPN2006-2010-142007)
- Deutscher Akademischer Austauschdienst (DAAD) [504 252 70]
DOI: 10.1016/j.tet.2011.10.011
ISSN: 0040-4020
WoS: 000297777700012
Scopus: 2-s2.0-80555122817
Институција/група
IHTMTY - JOUR AU - Stojanović, Milovan AU - Marković, Rade AU - Kleinpeter, Erich AU - Baranac-Stojanović, Marija PY - 2011 UR - https://cer.ihtm.bg.ac.rs/handle/123456789/814 AB - endo-Mode cyclizations of vinylogous N-acyliminium ions incorporating heteroatom-based nucleophiles have been examined as a route to the synthesis of condensed thiazolidines. The scope of these reactions and stereochemical outcome are discussed and explained using quantum chemical calculations. PB - Oxford : Pergamon-Elsevier Science Ltd T2 - Tetrahedron T1 - endo-Mode cyclizations of vinylogous N-acyliminium ions as a route to the synthesis of condensed thiazolidines VL - 67 IS - 49 SP - 9541 EP - 9554 DO - 10.1016/j.tet.2011.10.011 ER -
@article{ author = "Stojanović, Milovan and Marković, Rade and Kleinpeter, Erich and Baranac-Stojanović, Marija", year = "2011", abstract = "endo-Mode cyclizations of vinylogous N-acyliminium ions incorporating heteroatom-based nucleophiles have been examined as a route to the synthesis of condensed thiazolidines. The scope of these reactions and stereochemical outcome are discussed and explained using quantum chemical calculations.", publisher = "Oxford : Pergamon-Elsevier Science Ltd", journal = "Tetrahedron", title = "endo-Mode cyclizations of vinylogous N-acyliminium ions as a route to the synthesis of condensed thiazolidines", volume = "67", number = "49", pages = "9541-9554", doi = "10.1016/j.tet.2011.10.011" }
Stojanović, M., Marković, R., Kleinpeter, E.,& Baranac-Stojanović, M.. (2011). endo-Mode cyclizations of vinylogous N-acyliminium ions as a route to the synthesis of condensed thiazolidines. in Tetrahedron Oxford : Pergamon-Elsevier Science Ltd., 67(49), 9541-9554. https://doi.org/10.1016/j.tet.2011.10.011
Stojanović M, Marković R, Kleinpeter E, Baranac-Stojanović M. endo-Mode cyclizations of vinylogous N-acyliminium ions as a route to the synthesis of condensed thiazolidines. in Tetrahedron. 2011;67(49):9541-9554. doi:10.1016/j.tet.2011.10.011 .
Stojanović, Milovan, Marković, Rade, Kleinpeter, Erich, Baranac-Stojanović, Marija, "endo-Mode cyclizations of vinylogous N-acyliminium ions as a route to the synthesis of condensed thiazolidines" in Tetrahedron, 67, no. 49 (2011):9541-9554, https://doi.org/10.1016/j.tet.2011.10.011 . .