4.8 Article

Smooth Isoindolinone Formation from Isopropyl Carbamates via Bischler-Napieralski-Type Cyclization

Journal

ORGANIC LETTERS
Volume 16, Issue 2, Pages 358-361

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol403142d

Keywords

-

Funding

  1. MEXT-Supported Program for the Strategic Research Foundation at Private Universities

Ask authors/readers for more resources

Isopropyl carbamates derived from benzylamines provide isoindolinones by treatment with phosphorus pentoxide at room temperature. Utility of this Bischler-Napieralski-type cyclization and a new mechanism involving a carbamoyl cation for rationalization of this smooth conversion are discussed.

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