4.4 Review

Desymmetrization of Cyclopentene-1,3-Diones via Alkylation, Arylation, Amidation and Cycloaddition Reactions

Journal

CHEMISTRYSELECT
Volume 5, Issue 45, Pages 14484-14509

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/slct.202003341

Keywords

Cyclopentene-1; 3-diones; Desymmetrization; Asymmetric synthesis; Alkylation; Cycloaddition

Funding

  1. Department of Chemistry, NIT Jamshedpur
  2. SERB-DST

Ask authors/readers for more resources

Desymmetrization of prochiral cyclopentene-1,3-diones for the synthesis of various natural products and moieties of pharmaceutically active compounds, is a very challenging and competitive area of research in organic synthesis now a days. It is a very powerful strategy to provide quaternary stereocenter having different functionality, which is very difficult to install by other C-C bond-forming methods. This review describes an elaborative discussion of desymmetrization of cyclopentene-1,3-diones (racemic and asymmetric) via different alkylation, arylation, amidation and cycloaddition process for the last decades.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available