4.8 Article

New methodology for the deoxygenative difluoromethylenation of aldehydes and ketones; Unexpected formation of tetrafluorocyclopropanes

Journal

ORGANIC LETTERS
Volume 7, Issue 4, Pages 721-724

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol047416s

Keywords

-

Funding

  1. NIGMS NIH HHS [GM 029332] Funding Source: Medline

Ask authors/readers for more resources

[GRAPHICS] Generation of difluoromethylene phosphorus ylides in the presence of aldehydes and ketones results in Wittig-type reactions to give gem-difluoroalkenes, Subsequent in situ addition of difluorocarbene (carbenoid) can occur (increased with triphenylphosphine and decreased with tributylphosphine) to give tetrafluorocyclopropanes.

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