Pyrrolidine derived thioureas as organocatalysts in the Michael reaction of vinyl sulfone. Structure-stereoselectivity study
Само за регистроване кориснике
2016
Чланак у часопису (Објављена верзија)
Метаподаци
Приказ свих података о документуАпстракт
Structural variations of the heterocyclic ring of the recently introduced pyrrolidine derived thiourea organocatalysts have been studied. The results showed that the stereoselectivity is highly dependent on the substitution pattern reaching a moderate level, while the yields were generally less influenced by the structural changes. The outlined results may be helpful in further exploration of the thiourea catalyst represented by structure II.
Извор:
Therapeutic Advances in Drug Safety, 2016, 27, 19, 990-997Издавач:
- Pergamon-Elsevier Science Ltd, Oxford
Финансирање / пројекти:
- Компјутерско дизајнирање, синтеза и биолошка евалуација нових хетероцикличних једињења као селективних инхибитора туморогенезе (RS-MESTD-Basic Research (BR or ON)-172009)
DOI: 10.1016/j.tetasy.2016.08.004
ISSN: 0957-4166
WoS: 000383817100012
Scopus: 2-s2.0-84984982209
Институција/група
PharmacyTY - JOUR AU - Jovanović, Predrag AU - Petković, Miloš AU - Ivković, Branka AU - Savić, Vladimir PY - 2016 UR - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2723 AB - Structural variations of the heterocyclic ring of the recently introduced pyrrolidine derived thiourea organocatalysts have been studied. The results showed that the stereoselectivity is highly dependent on the substitution pattern reaching a moderate level, while the yields were generally less influenced by the structural changes. The outlined results may be helpful in further exploration of the thiourea catalyst represented by structure II. PB - Pergamon-Elsevier Science Ltd, Oxford T2 - Therapeutic Advances in Drug Safety T1 - Pyrrolidine derived thioureas as organocatalysts in the Michael reaction of vinyl sulfone. Structure-stereoselectivity study VL - 27 IS - 19 SP - 990 EP - 997 DO - 10.1016/j.tetasy.2016.08.004 ER -
@article{ author = "Jovanović, Predrag and Petković, Miloš and Ivković, Branka and Savić, Vladimir", year = "2016", abstract = "Structural variations of the heterocyclic ring of the recently introduced pyrrolidine derived thiourea organocatalysts have been studied. The results showed that the stereoselectivity is highly dependent on the substitution pattern reaching a moderate level, while the yields were generally less influenced by the structural changes. The outlined results may be helpful in further exploration of the thiourea catalyst represented by structure II.", publisher = "Pergamon-Elsevier Science Ltd, Oxford", journal = "Therapeutic Advances in Drug Safety", title = "Pyrrolidine derived thioureas as organocatalysts in the Michael reaction of vinyl sulfone. Structure-stereoselectivity study", volume = "27", number = "19", pages = "990-997", doi = "10.1016/j.tetasy.2016.08.004" }
Jovanović, P., Petković, M., Ivković, B.,& Savić, V.. (2016). Pyrrolidine derived thioureas as organocatalysts in the Michael reaction of vinyl sulfone. Structure-stereoselectivity study. in Therapeutic Advances in Drug Safety Pergamon-Elsevier Science Ltd, Oxford., 27(19), 990-997. https://doi.org/10.1016/j.tetasy.2016.08.004
Jovanović P, Petković M, Ivković B, Savić V. Pyrrolidine derived thioureas as organocatalysts in the Michael reaction of vinyl sulfone. Structure-stereoselectivity study. in Therapeutic Advances in Drug Safety. 2016;27(19):990-997. doi:10.1016/j.tetasy.2016.08.004 .
Jovanović, Predrag, Petković, Miloš, Ivković, Branka, Savić, Vladimir, "Pyrrolidine derived thioureas as organocatalysts in the Michael reaction of vinyl sulfone. Structure-stereoselectivity study" in Therapeutic Advances in Drug Safety, 27, no. 19 (2016):990-997, https://doi.org/10.1016/j.tetasy.2016.08.004 . .