Literature DB >> 20063859

Highly enantioselective Diels-Alder reactions of maleimides catalyzed by activated chiral oxazaborolidines.

Santanu Mukherjee1, E J Corey.   

Abstract

Diels-Alder reactions of various combinations of maleimides and 1,3-dienes with cationic oxazaborolidines as catalysts have been shown to be highly efficient and enantioselective.

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Year:  2010        PMID： 20063859     DOI： 10.1021/ol902865d

Source DB:  PubMed          Journal:  Org Lett        ISSN： 1523-7052            Impact factor:   6.005


  3 in total

1.  Total Synthesis of the Diterpenoid Alkaloid Arcutinidine Using a Strategy Inspired by Chemical Network Analysis.

Authors:  Kyle R Owens; Shelby V McCowen; Katherine A Blackford; Sohei Ueno; Yasuo Hirooka; Manuel Weber; Richmond Sarpong
Journal:  J Am Chem Soc       Date:  2019-08-21       Impact factor: 15.419

2.  Synthesis of Succinimide-Linked Indazol-3-ols Derived from Maleimides under Rh(III) Catalysis.

Authors:  Ju Young Kang; Suho Kim; Junghyea Moon; Eunjae Chung; Jaeyoung Kim; So Young Kyung; Hyung Sik Kim; Neeraj Kumar Mishra; In Su Kim
Journal:  ACS Omega       Date:  2022-04-21

3.  Peptide-Catalyzed Stereoselective Conjugate Addition Reaction of Aldehydes to C-Substituted Maleimides.

Authors:  Greta Vastakaite; Claudio E Grünenfelder; Helma Wennemers
Journal:  Chemistry       Date:  2022-02-28       Impact factor: 5.020
  3 in total

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