4.8 Article

Termination of Mn(III)-based oxidative cyclizations by trapping with azide

Journal

ORGANIC LETTERS
Volume 6, Issue 8, Pages 1265-1268

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol049805s

Keywords

-

Funding

  1. NIGMS NIH HHS [GM 50101] Funding Source: Medline

Ask authors/readers for more resources

[GRAPHICS] The radicals formed in Mn(III)-based oxidative free-radical cyclizations of beta-keto esters and malonate esters can be trapped with sodium azide and Mn(ill) to give cyclic and bicyclic azides in 30-80% yield. Reduction of the azide gives bi- and tricyclic lactams.

Authors

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

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available