دورية أكاديمية

Stereospecific Oxidation of Diacetoxyheterobetulin with Ozone and Dimethyldioxirane.

التفاصيل البيبلوغرافية
العنوان: Stereospecific Oxidation of Diacetoxyheterobetulin with Ozone and Dimethyldioxirane.
المؤلفون: Khusnutdinova EF, Medvedeva NI, Kazakov DV, Kukovinets OS, Lobov AN, Suponitsky KY, Kazakov OB
المصدر: Natural product communications [Nat Prod Commun] 2016 Apr; Vol. 11 (4), pp. 449-52.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: SAGE Publications Country of Publication: United States NLM ID: 101477873 Publication Model: Print Cited Medium: Print ISSN: 1934-578X (Print) Linking ISSN: 15559475 NLM ISO Abbreviation: Nat Prod Commun Subsets: MEDLINE
أسماء مطبوعة: Publication: 2019- : [Thousand Oaks, CA] : SAGE Publications
Original Publication: Westerville, OH : Natural Product Communications, [2006]-[2018]
مواضيع طبية MeSH: Epoxy Compounds/*chemical synthesis , Epoxy Compounds/*chemistry , Triterpenes/*chemical synthesis , Triterpenes/*chemistry, Oxidation-Reduction ; Ozone/chemistry ; Stereoisomerism
مستخلص: Stereospecific oxidation of diacetoxyheterobetulin with ozone and dimethyldioxirane led to 3β,28-diacetoxy-18α,19βH-urs-20α,21α-epoxide with yields of 79% and 87%, respectively. Oxidation with ozone was not selective and gave two minor products containing 2lα-hydroxy-20(30)-ene and 21a-hydroxy-20β,28-epoxy-fragments in ring E. The structures of 3β,28-diacetoxy-18α,19βH-urs-20α,21α-epoxide and 3β-diacetoxy-21α-hydroxy-20β,28-epoxy-18α,19βH-ursane were confirmed by X-ray analysis for the first time.
المشرفين على المادة: 0 (3beta,28-diacetoxy-18alpha,19betaH-urs-20alpha,21alpha-epoxide)
0 (Epoxy Compounds)
0 (Triterpenes)
0 (diacetoxyheterobetulin)
66H7ZZK23N (Ozone)
R5RAT196DJ (dimethyldioxirane)
تواريخ الأحداث: Date Created: 20160712 Date Completed: 20160929 Latest Revision: 20171116
رمز التحديث: 20240628
PMID: 27396190
قاعدة البيانات: MEDLINE