Regio- and stereoselective behavior of l-arabinal-derived vinyl epoxide in nucleophilic addition reactions. Comparison with conformationally restricted d-galactal-derived analogs-Reference-Cited by-同舟云学术

Regio- and stereoselective behavior of l-arabinal-derived vinyl epoxide in nucleophilic addition reactions. Comparison with conformationally restricted d-galactal-derived analogs

Published:2015-09 Issue:36 Volume:71 Page:6276-6284
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Di Bussolo Valeria,Frau Ileana,Favero Lucilla,Uccello-Barretta Gloria,Balzano Federica,Crotti Paolo

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference17 articles.

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

2. New Stereoselective β-Glycosylation via a Vinyl Oxirane Derived from d-Glucal

3. New Stereoselective β-C-Glycosidation by Uncatalyzed 1,4-Addition of Organolithium Reagents to a Glycal-Derived Vinyl Oxirane

4. Synthesis of diastereoisomeric 6-deoxy-d-allal- and 6-deoxy-d-galactal-derived allyl epoxides and examination of the regio- and stereoselectivity in nucleophilic addition reactions. Comparison with the corresponding 6-O-functionalized allyl epoxides

5. Theoretical conformational study of six-membered cyclic allyl epoxides

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