A short and common stereoselective approach to 5/6, 6/6, 6/7 bicyclic aza sugars

Autor:	K. Veera Mohana Rao, Bandari Chandrasekhar, Bharatam Jagadeesh, B. Venkateswara Rao
Rok vydání:	2009
Předmět:	Inorganic Chemistry chemistry.chemical_compound Ring-closing metathesis Bicyclic molecule Chemistry Stereochemistry Organic Chemistry Imine Grignard reaction Stereoselectivity Physical and Theoretical Chemistry Catalysis
Zdroj:	Tetrahedron: Asymmetry. 20:1217-1223
ISSN:	0957-4166
DOI:	10.1016/j.tetasy.2009.03.038
Popis:	An efficient and highly stereoselective approach to bicyclic aza sugars is described using Grignard reaction on an N-benzyl imine derived from 3-O-benzyl-1,2-O-isopropylidine-α- d -xylo-pentodialdofuranose, ring closing metathesis, and reductive cyclization as key steps.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::593696448d4c22e4b13bf9745ce4ac8e https://doi.org/10.1016/j.tetasy.2009.03.038 Zobrazit plný text záznamu Full Text from ScienceDirect