Loading…

Catalytic Asymmetric Darzens and Aza‐Darzens Reactions for the Synthesis of Chiral Epoxides and Aziridines

This review presents an overview on the recent advances in the catalytic enantioselective Darzens and aza‐Darzens reactions for the synthesis of enantiopure three‐membered oxygen and nitrogen containing heterocycles. Since the synthesis of epoxides is the most widely explored, compared to their nitr...

Full description

Saved in:
Bibliographic Details
Published in:ChemCatChem 2018-11, Vol.10 (22), p.5092-5114
Main Authors: de los Santos, Jesús M., Ochoa de Retana, Ana M., Martínez de Marigorta, Edorta, Vicario, Javier, Palacios, Francisco
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:This review presents an overview on the recent advances in the catalytic enantioselective Darzens and aza‐Darzens reactions for the synthesis of enantiopure three‐membered oxygen and nitrogen containing heterocycles. Since the synthesis of epoxides is the most widely explored, compared to their nitrogen counterparts, particularly true when asymmetric synthesis are considered, in the last decades several methodologies have appeared or improved and are now available for the preparation of aziridines in a highly stereo‐ and enantioselective manner. Catalytic asymmetric Darzens and aza‐Darzens reaction constitute an important tool in modern organic chemistry, as there is an increased interest in bioactive natural products and pharmaceutical agents that contain these skeletons. Chiral epoxides and aziridines: In the last decades several methodologies have appeared or improved and are now available for the preparation of epoxides and aziridines in a highly stereo‐ and enantioselective manner. This review covers the most recent advances related to the catalytic enantioselective Darzens and aza‐Darzens reactions for the synthesis of chiral epoxides and aziridines.
ISSN:1867-3880
1867-3899
DOI:10.1002/cctc.201801026