Synthesis of carba analogs of 6-O-(benzyl)-d-allal- and -d-galactal-derived allyl epoxides and evaluation of the regio- and stereoselective behavior in nucleophilic addition reactions-Reference-Cited by-同舟云学术

Synthesis of carba analogs of 6-O-(benzyl)-d-allal- and -d-galactal-derived allyl epoxides and evaluation of the regio- and stereoselective behavior in nucleophilic addition reactions

Published:2011-06 Issue:25 Volume:67 Page:4696-4709
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Di Bussolo Valeria,Frau Ileana,Checchia Lorenzo,Favero Lucilla,Pineschi Mauro,Uccello-Barretta Gloria,Balzano Federica,Roselli Graziella,Renzi Gabriele,Crotti Paolo

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference28 articles.

1. Synthesis and Conformational and Biological Aspects of Carbasugars

2. Naturally Occurring Cyclohexane Epoxides: Sources, Biological Activities, and Synthesis

3. Synthesis of carbasugar-containing non-glycosidically linked pseudodisaccharides and higher pseudooligosaccharides

4. Stereospecific Uncatalyzed α-O-Glycosylation and α-C-Glycosidation by Means of a New d-Gulal-Derived α Vinyl Oxirane

5. Regio- and Stereoselectivity of the Addition of O-, S-, N-, and C-Nucleophiles to the β Vinyl Oxirane Derived from d-Glucal

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