دورية أكاديمية

Organocatalytic and enantioselective Michael reaction between α-nitroesters and nitroalkenes. Syn/anti-selectivity control using catalysts with the same absolute backbone chirality

التفاصيل البيبلوغرافية
العنوان: Organocatalytic and enantioselective Michael reaction between α-nitroesters and nitroalkenes. Syn/anti-selectivity control using catalysts with the same absolute backbone chirality
المؤلفون: Jose I. Martínez, Uxue Uria, Maria Muñiz, Efraím Reyes, Luisa Carrillo, Jose L. Vicario
المصدر: Beilstein Journal of Organic Chemistry, Vol 11, Iss 1, Pp 2577-2583 (2015)
بيانات النشر: Beilstein-Institut, 2015.
سنة النشر: 2015
المجموعة: LCC:Science
LCC:Organic chemistry
مصطلحات موضوعية: asymmetric diastereodivergent, enantioselective, Michael addition, nitroalkenes, nitroesters, organocatalysis, squaramides, Science, Organic chemistry, QD241-441
الوصف: The asymmetric and catalytic Michael reaction between α-nitroesters and nitroalkenes has been studied in the presence of two bifunctional catalysts both containing the same absolute chirality at the carbon backbone. The reaction performed in similar conditions allows us to control the syn or anti selectivity of the Michael adduct obtaining good yields and high enantiocontrol in all cases.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1860-5397
Relation: https://doaj.org/toc/1860-5397
DOI: 10.3762/bjoc.11.277
URL الوصول: https://doaj.org/article/fd9be3fbe978495d93839551d964679f
رقم الأكسشن: edsdoj.fd9be3fbe978495d93839551d964679f
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:18605397
DOI:10.3762/bjoc.11.277