Open Access Open Access  Restricted Access Subscription Access

ASYMMETRIC REACTIONS EMPLOYING 1,3-DIPOLES

Albert Padwa, Scott Bur
Cover Image

Abstract


The preparation of heterocyclic compounds using 1,3-dipolar cycloaddition chemistry is now well recognized in the fields of organic synthesis, drug discovery efforts, polymer chemistry, and materials science. As highlighted in this review, a growing area of interest in organic synthesis involves the enantioselectivity aspects of dipolar cycloaddition chemistry for the preparation of many different classes of natural products. Asymmetric synthesis of natural products using chiral substrates has been elegantly accomplished over the past decade using an assortment of dipole intermediates and represents the focus of this review article.

 


Keywords


azomethine imines; azomethine ylides; carbonyl ylides; diazoalkanes; 1,3-dipoles; nitrones; asymmetric synthesis; cycloaddition

Full Text: PDF Supplementary File(s): None


 

 

Latvian Institute of Organic Synthesis - Aizkraukles iela, 21, Riga, LV-1006, Latvia - hgs@osi.lv