دورية أكاديمية

cis–trans Isomerization of silybins A and B

التفاصيل البيبلوغرافية
العنوان: cis–trans Isomerization of silybins A and B
المؤلفون: Michaela Novotná, Radek Gažák, David Biedermann, Florent Di Meo, Petr Marhol, Marek Kuzma, Lucie Bednárová, Kateřina Fuksová, Patrick Trouillas, Vladimír Křen
المصدر: Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 1047-1063 (2014)
بيانات النشر: Beilstein-Institut, 2014.
سنة النشر: 2014
المجموعة: LCC:Science
LCC:Organic chemistry
مصطلحات موضوعية: 2,3-cis-silybin, 10,11-cis-silybin, isomerization, silibinin, silybin, silymarin, Science, Organic chemistry, QD241-441
الوصف: Methods were developed and optimized for the preparation of the 2,3-cis- and the 10,11-cis-isomers of silybin by the Lewis acid catalyzed (BF3∙OEt2) isomerization of silybins A (1a) and B (1b) (trans-isomers). The absolute configuration of all optically pure compounds was determined by using NMR and comparing their electronic circular dichroism data with model compounds of known absolute configurations. Mechanisms for cis–trans-isomerization of silybin are proposed and supported by quantum mechanical calculations.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1860-5397
Relation: https://doaj.org/toc/1860-5397
DOI: 10.3762/bjoc.10.105
URL الوصول: https://doaj.org/article/32eceaea79cc4b569924581b8eaffe3e
رقم الأكسشن: edsdoj.32eceaea79cc4b569924581b8eaffe3e
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:18605397
DOI:10.3762/bjoc.10.105