4.8 Article

Gold/Lewis Acid Catalyzed Cycloisomerization/Diastereoselective [3+2] Cycloaddition Cascade: Synthesis of Diverse Nitrogen-Containing Spiro Heterocycles

Journal

ORGANIC LETTERS
Volume 18, Issue 18, Pages 4614-4617

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b02253

Keywords

-

Funding

  1. Natural Science Foundation of China [21572118, JQ201505]
  2. Natural Science Foundation of Shandong province [21572118, JQ201505]
  3. fundamental research and subject construction funds [2014JC008, 104.205.2.5]
  4. Zhong-Ying scholar award of Shandong University

Ask authors/readers for more resources

A novel early and late transition-metal relay catalysis has been developed by combining a gold-catalyzed Cydoisomerization and a Yb(OTf)(3)-catalyzed diastereoselective [3 + 2] cycloaddition with aziridines in a selective C-C bond cleavage mode. Various biologically significant complex nitrogen-containing spiro heterocycles were rapidly constructed from readily available starting materials under mild conditions.

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