4.7 Article

Synthesis of a new spiro-BOX ligand and its application in enantioselective allylic cyclization based on carbopalladation of allenyl hydrazines

Journal

CHEMICAL COMMUNICATIONS
Volume -, Issue 41, Pages 6198-6200

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/b912108k

Keywords

-

Funding

  1. National Natural Science Foundation of China [20732005]
  2. State Basic Research and Development Program [2006CB806105]
  3. Chinese Academy of Sciences

Ask authors/readers for more resources

In this paper, we developed a new bisoxazoline ligand with a spiro skeleton and a alpha-naphthylmethyl substituent, i.e. (R-a,S,S)-L3, which has been successfully applied to the highly enantioselective cyclic allylation based on the carbopalladation of 3,4-allenyl hydrazines with ee values ranging from 92-95%.

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