4.7 Article

Synthesis and decarboxylative Wittig reaction of difluoromethylene phosphobetaine

Journal

CHEMICAL COMMUNICATIONS
Volume 49, Issue 68, Pages 7513-7515

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c3cc44271c

Keywords

-

Funding

  1. 973 Program of China [2012CBA01200]

Ask authors/readers for more resources

A key intermediate, difluoromethylene phosphobetaine, in the Wittig reaction of ClCF2CO2Na-Ph3P with aldehydes was synthesized and characterized, which confirmed the reaction mechanism. The decarboxylation of this stable intermediate was a convenient approach for Wittig difluroolefination. Its reactivity could be adjusted by the modification of the substituent on the phosphorus.

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