Highly enantioselective synthesis of isoxazoline N-oxides.

Chem Commun (Camb)

State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, China.

Published: February 2008

AI Article Synopsis

  • A method has been created using cinchonidine (or cinchonine) ammonium salts to react with nitroolefins.
  • This process takes place in the presence of Cs2CO3.
  • The result is the production of optically active isoxazoline N-oxides with high enantiomeric excess (ee) and good diastereomeric values (de).

Article Abstract

The reaction of cinchonidine (cinchonine)-derived ammonium salts with nitroolefins in the presence of Cs2CO3 to afford optically active isoxazoline N-oxides with excellent ee and high de values has been developed.

Download full-text PDF

Source
http://dx.doi.org/10.1039/b716468hDOI Listing

Publication Analysis

Top Keywords

isoxazoline n-oxides
8
highly enantioselective
4
enantioselective synthesis
4
synthesis isoxazoline
4
n-oxides reaction
4
reaction cinchonidine
4
cinchonidine cinchonine-derived
4
cinchonine-derived ammonium
4
ammonium salts
4
salts nitroolefins
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!