دورية أكاديمية

Transannular dipolar cycloaddition as an approach towards the synthesis of the core ring system of the sarain alkaloids.

التفاصيل البيبلوغرافية
العنوان: Transannular dipolar cycloaddition as an approach towards the synthesis of the core ring system of the sarain alkaloids.
المؤلفون: Franklin AI; Department of Chemistry, University of Sheffield, Brook Hill, Sheffield, UK S3 7HF., Bensa D, Adams H, Coldham I
المصدر: Organic & biomolecular chemistry [Org Biomol Chem] 2011 Mar 21; Vol. 9 (6), pp. 1901-7. Date of Electronic Publication: 2011 Jan 31.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Royal Society of Chemistry Country of Publication: England NLM ID: 101154995 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1477-0539 (Electronic) Linking ISSN: 14770520 NLM ISO Abbreviation: Org Biomol Chem Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Cambridge, UK : Royal Society of Chemistry, c2003-
مواضيع طبية MeSH: Alkaloids/*chemical synthesis , Bridged-Ring Compounds/*chemical synthesis, Crystallography, X-Ray ; Cyclization ; Models, Molecular ; Molecular Structure
مستخلص: Intramolecular transannular dipolar cycloaddition was investigated as a key step in a synthetic approach to the core of the sarain alkaloids; although the use of an azomethine ylide was unsuccessful with the chosen aldehyde substrate, cycloaddition with a nitrone did give the alternative regioisomeric bridged cycloadduct.
المشرفين على المادة: 0 (Alkaloids)
0 (Bridged-Ring Compounds)
تواريخ الأحداث: Date Created: 20110202 Date Completed: 20110425 Latest Revision: 20161125
رمز التحديث: 20221213
DOI: 10.1039/c0ob01019g
PMID: 21283902
قاعدة البيانات: MEDLINE
الوصف
تدمد:1477-0539
DOI:10.1039/c0ob01019g