A stereodivergent approach to carbahexofuranoses: synthesis of carba-α-d-glucofuranose, carba-β-d-altrofuranose, carba-α-d-allofuranose, carba-β-d-idofuranose, carba-α-d-galactofuranose and carba-β-d-talofuranose

Autor:	Deekshaputra R. Birhade, Attrimuni P. Dhondge, Mukund G. Kulkarni, Nagorao R. Dhatrak, Ajit S. Borhade, Yunnus B. Shaikh
Rok vydání:	2011
Předmět:	Claisen rearrangement chemistry.chemical_compound Ring-closing metathesis chemistry Stereochemistry Glyceraldehyde Organic Chemistry Drug Discovery Wittig reaction Biochemistry Derivative (chemistry)
Zdroj:	Tetrahedron Letters. 52:5559-5562
ISSN:	0040-4039
Popis:	A stereodivergent route, starting from d -glyceraldehyde derivative, employing Wittig olefination–Claisen rearrangement protocol is reported for the synthesis of six novel carbahexofuranoses—carba-α- d -glucofuranose, carba-β- d -altrofuranose, carba-α- d -allofuranose, carba-β- d -idofuranose, carba-α- d -galactofuranose and carba-β- d -talofuranose in enantiomerically pure form.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::1233c6149bd8ded138a77013af5454ba https://doi.org/10.1016/j.tetlet.2011.08.006 Zobrazit plný text záznamu Full Text from ScienceDirect