دورية أكاديمية
Transannular dipolar cycloaddition as an approach towards the synthesis of the core ring system of the sarain alkaloids.
العنوان: | Transannular dipolar cycloaddition as an approach towards the synthesis of the core ring system of the sarain alkaloids. |
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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 |
تدمد: | 1477-0539 |
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DOI: | 10.1039/c0ob01019g |