Synthesis of the first thiazolidine-condensed five-, six-, and seven-membered heterocycles via cyclization of vinylogous N-acyliminium ions
Samo za registrovane korisnike
2009
Članak u časopisu (Objavljena verzija)
Metapodaci
Prikaz svih podataka o dokumentuApstrakt
Synthesis of new thiazolidine-fused five-, six-, and seven-membered heterocycles through vinylogous N-acyliminium ion-cyclization sequence, involving positions 3 and 4 of the thiazolidine ring, is described. The formation of bicyclic products, arising by generally disfavored 5-endo-trig cyclization initiated by sulfur atom acting as a nucleophile, indicates the preparative value of this method.
Ključne reči:
Cyclization / Fused-ring systems / Iminium ions / Lactams / Neighboring-group effectsIzvor:
Synlett, 2009, 12, 1997-2001Finansiranje / projekti:
- Tiazolidni i sintetički analozi: reaktivnost, primena i biološka aktivnost (RS-MESTD-MPN2006-2010-142007)
DOI: 10.1055/s-0029-1217532
ISSN: 0936-5214
WoS: 000269337500023
Scopus: 2-s2.0-67651208211
Institucija/grupa
IHTMTY - JOUR AU - Stojanović, Milovan AU - Marković, Rade PY - 2009 UR - https://cer.ihtm.bg.ac.rs/handle/123456789/580 AB - Synthesis of new thiazolidine-fused five-, six-, and seven-membered heterocycles through vinylogous N-acyliminium ion-cyclization sequence, involving positions 3 and 4 of the thiazolidine ring, is described. The formation of bicyclic products, arising by generally disfavored 5-endo-trig cyclization initiated by sulfur atom acting as a nucleophile, indicates the preparative value of this method. T2 - Synlett T1 - Synthesis of the first thiazolidine-condensed five-, six-, and seven-membered heterocycles via cyclization of vinylogous N-acyliminium ions IS - 12 SP - 1997 EP - 2001 DO - 10.1055/s-0029-1217532 ER -
@article{ author = "Stojanović, Milovan and Marković, Rade", year = "2009", abstract = "Synthesis of new thiazolidine-fused five-, six-, and seven-membered heterocycles through vinylogous N-acyliminium ion-cyclization sequence, involving positions 3 and 4 of the thiazolidine ring, is described. The formation of bicyclic products, arising by generally disfavored 5-endo-trig cyclization initiated by sulfur atom acting as a nucleophile, indicates the preparative value of this method.", journal = "Synlett", title = "Synthesis of the first thiazolidine-condensed five-, six-, and seven-membered heterocycles via cyclization of vinylogous N-acyliminium ions", number = "12", pages = "1997-2001", doi = "10.1055/s-0029-1217532" }
Stojanović, M.,& Marković, R.. (2009). Synthesis of the first thiazolidine-condensed five-, six-, and seven-membered heterocycles via cyclization of vinylogous N-acyliminium ions. in Synlett(12), 1997-2001. https://doi.org/10.1055/s-0029-1217532
Stojanović M, Marković R. Synthesis of the first thiazolidine-condensed five-, six-, and seven-membered heterocycles via cyclization of vinylogous N-acyliminium ions. in Synlett. 2009;(12):1997-2001. doi:10.1055/s-0029-1217532 .
Stojanović, Milovan, Marković, Rade, "Synthesis of the first thiazolidine-condensed five-, six-, and seven-membered heterocycles via cyclization of vinylogous N-acyliminium ions" in Synlett, no. 12 (2009):1997-2001, https://doi.org/10.1055/s-0029-1217532 . .