4.8 Article

Synthesis of Pyrroles by Gold(I)-Catalyzed Amino-Claisen Rearrangement of N-Propargyl Enaminone Derivatives

Journal

ORGANIC LETTERS
Volume 12, Issue 2, Pages 372-374

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol902716n

Keywords

-

Funding

  1. MEXT Japan [21790024]
  2. Central Glass Co., Ltd
  3. Grants-in-Aid for Scientific Research [21790024] Funding Source: KAKEN

Ask authors/readers for more resources

The cationic N-heterocyclic carbene-gold(I) complex catalyzes the formation of tri- and tetrasubstituted pyrroles via the amino-Claisen rearrangement of N-propargyl beta-enaminone derivatives and the cyclization of alpha-allenyl beta-enaminone Intermediates.

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