Pyrrolidine derived thioureas as organocatalysts in the Michael reaction of vinyl sulfone. Structure-stereoselectivity study
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.
Source:
Therapeutic Advances in Drug Safety, 2016, 27, 19, 990-997Publisher:
- Pergamon-Elsevier Science Ltd, Oxford
Funding / projects:
DOI: 10.1016/j.tetasy.2016.08.004
ISSN: 0957-4166
WoS: 000383817100012
Scopus: 2-s2.0-84984982209
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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 . .