دورية أكاديمية
Stereospecific Oxidation of Diacetoxyheterobetulin with Ozone and Dimethyldioxirane.
العنوان: | Stereospecific Oxidation of Diacetoxyheterobetulin with Ozone and Dimethyldioxirane. |
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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 |
تدمد: | 1934-578X |
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