4.7 Article

Regio- and stereoselectivity of the addition of O-, S-, N-, and C-nucleophiles to the β vinyl oxirane derived from D-glucal

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 69, Issue 25, Pages 8702-8708

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jo048981b

Keywords

-

Ask authors/readers for more resources

6-O-Trityl- (1a) and 6-(O-benzyl)-substituted epoxide (1b) derived from D-glucal were examined in their addition reactions with O-, C-, N-, and S-nucleophiles. A 1,4-regio- and beta-stereoselective or an anti 1,2-addition pathway is commonly observed depending on the ability of the nucleophile to coordinate with the oxirane oxygen. When TMSN3 or LiN3 are used as azide-based nucleophiles, a 1,2-syn-addition pathway is also observed,

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available