4.4 Article

Recent advances in metal carbenoid mediated nitrogen-containing zwitterionic intermediate trapping process

Journal

TETRAHEDRON LETTERS
Volume 55, Issue 4, Pages 777-783

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2013.12.026

Keywords

Carbenoid; Diazo compound; Zwitterionic intermediate; Trapping process; Enamine

Ask authors/readers for more resources

Zwitterionic intermediates generated from metal carbenoids and compounds containing enamine units belong to a class of highly active synthetic intermediates that undergo different types of transformations. They can undergo rapid proton transfer to afford C-H functionalization products, or undergo intramolecular trapping process to give [3+2] annulation products. Recently, by taking advantage of its unique electronic feature, novel transformations have been developed by applying suitable electrophiles to trap such type of zwitterionic intermediates. The successful trapping process offers a powerful strategy for the effective construction of diversified nitrogen-containing molecules. (C) 2013 Elsevier Ltd. All rights reserved.

Authors

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

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available