4.7 Article

Recent Developments in the Catalytic, Asymmetric Construction of Pyrroloindolines Bearing All-Carbon Quaternary Stereocenters

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 78, Issue 24, Pages 12314-12320

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jo4017953

Keywords

-

Funding

  1. California Institute of Technology
  2. NIH [NIGMS RGM097582A]
  3. Baxter Foundation
  4. Amgen
  5. Boehringer Ingelheim
  6. ACS Petroleum Research Foundation
  7. ACS Division of Organic Chemistry sponsored by Genentech

Ask authors/readers for more resources

Pyrroloindoline alkaloids constitute a large family of natural products that has inspired the development of an impressive array of new reactions to prepare the key heterocyclic motif. This synopsis will address catalytic, asymmetric reactions developed to synthesize pyrroloindolines bearing C3a all-carbon quaternary stereocenters. The methods described herein include both transition-metal-catalyzed and organocatalyzed reactions that have been demonstrated to be suitable for the synthesis of the pyrroloindoline framework.

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