Catalytic Enantioselective Isocyanide‐Based Reactions: Beyond Passerini and Ugi Multicomponent Reactions

The development of catalytic enantioselective isocyanide‐based reactions is currently of great interest because the resulting products are valuable in organic synthesis, pharmacological chemistry, and materials science. This review assembles and comprehensively summarizes the recent achievements in...

Full description

Saved in:
Bibliographic Details
Published inChemistry : a European journal Vol. 27; no. 22; pp. 6598 - 6619
Main Authors Luo, Jian, Chen, Guo‐Shu, Chen, Shu‐Jie, Li, Zhao‐Dong, Liu, Yun‐Lin
Format Journal Article
LanguageEnglish
Published Germany Wiley Subscription Services, Inc 16.04.2021
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The development of catalytic enantioselective isocyanide‐based reactions is currently of great interest because the resulting products are valuable in organic synthesis, pharmacological chemistry, and materials science. This review assembles and comprehensively summarizes the recent achievements in this rapidly growing area according to the reaction types. Special attention is paid to the advantages, limitations, possible mechanisms, and synthetic applications of each reaction. In addition, a personal outlook on the opportunities for further exploration is given at the end. Isocyanide‐based reactions: The development of catalytic enantioselective isocyanide‐based reactions is currently of great interest because the resulting products are valuable in organic synthesis, pharmacological chemistry, and materials science. This review assembles and comprehensively summarizes the recent achievements in this rapidly growing area according to the reaction types. Special attention is paid to the advantages, limitations, possible mechanisms, and synthetic applications of each reaction. In addition, a personal outlook on the opportunities for further exploration is given.
Bibliography:These authors contributed equally to this work.
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-3
content type line 23
ObjectType-Review-1
ISSN:0947-6539
1521-3765
DOI:10.1002/chem.202003224