Substituted proline derivatives as organocatalysts in the Michael reaction
2014
Аутори
Jovanović, PredragRanđelović, Jelena
Ivković, Branka
Suteu, Cristina
Tokić-Vujošević, Zorana
Savić, Vladimir
Чланак у часопису (Објављена верзија)
Метаподаци
Приказ свих података о документуАпстракт
Chiral, polysubstituted proline esters, obtained via cycloaddition reactions of azomethine ylides, were studied as organocatalysts in the Michael reaction of aldehydes/ketones and vinylsulphones. Under optimised reaction conditions employing 10 mol % of the catalyst in wet CH2Cl2, the yields of the products were generally good while the enantioselectivity varied, reaching up to 52 %.
Кључне речи:
Michael reaction / organocatalysis / proline derivativesИзвор:
Journal of the Serbian Chemical Society, 2014, 79, 7, 767-778Издавач:
- Srpsko hemijsko društvo, Beograd
Финансирање / пројекти:
- Компјутерско дизајнирање, синтеза и биолошка евалуација нових хетероцикличних једињења као селективних инхибитора туморогенезе (RS-MESTD-Basic Research (BR or ON)-172009)
DOI: 10.2298/JSC131015002J
ISSN: 0352-5139
WoS: 000339931600002
Scopus: 2-s2.0-84940265994
Институција/група
PharmacyTY - JOUR AU - Jovanović, Predrag AU - Ranđelović, Jelena AU - Ivković, Branka AU - Suteu, Cristina AU - Tokić-Vujošević, Zorana AU - Savić, Vladimir PY - 2014 UR - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2098 AB - Chiral, polysubstituted proline esters, obtained via cycloaddition reactions of azomethine ylides, were studied as organocatalysts in the Michael reaction of aldehydes/ketones and vinylsulphones. Under optimised reaction conditions employing 10 mol % of the catalyst in wet CH2Cl2, the yields of the products were generally good while the enantioselectivity varied, reaching up to 52 %. PB - Srpsko hemijsko društvo, Beograd T2 - Journal of the Serbian Chemical Society T1 - Substituted proline derivatives as organocatalysts in the Michael reaction VL - 79 IS - 7 SP - 767 EP - 778 DO - 10.2298/JSC131015002J ER -
@article{ author = "Jovanović, Predrag and Ranđelović, Jelena and Ivković, Branka and Suteu, Cristina and Tokić-Vujošević, Zorana and Savić, Vladimir", year = "2014", abstract = "Chiral, polysubstituted proline esters, obtained via cycloaddition reactions of azomethine ylides, were studied as organocatalysts in the Michael reaction of aldehydes/ketones and vinylsulphones. Under optimised reaction conditions employing 10 mol % of the catalyst in wet CH2Cl2, the yields of the products were generally good while the enantioselectivity varied, reaching up to 52 %.", publisher = "Srpsko hemijsko društvo, Beograd", journal = "Journal of the Serbian Chemical Society", title = "Substituted proline derivatives as organocatalysts in the Michael reaction", volume = "79", number = "7", pages = "767-778", doi = "10.2298/JSC131015002J" }
Jovanović, P., Ranđelović, J., Ivković, B., Suteu, C., Tokić-Vujošević, Z.,& Savić, V.. (2014). Substituted proline derivatives as organocatalysts in the Michael reaction. in Journal of the Serbian Chemical Society Srpsko hemijsko društvo, Beograd., 79(7), 767-778. https://doi.org/10.2298/JSC131015002J
Jovanović P, Ranđelović J, Ivković B, Suteu C, Tokić-Vujošević Z, Savić V. Substituted proline derivatives as organocatalysts in the Michael reaction. in Journal of the Serbian Chemical Society. 2014;79(7):767-778. doi:10.2298/JSC131015002J .
Jovanović, Predrag, Ranđelović, Jelena, Ivković, Branka, Suteu, Cristina, Tokić-Vujošević, Zorana, Savić, Vladimir, "Substituted proline derivatives as organocatalysts in the Michael reaction" in Journal of the Serbian Chemical Society, 79, no. 7 (2014):767-778, https://doi.org/10.2298/JSC131015002J . .