4.4 Review

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

期刊

CHEMISTRYSELECT
卷 5, 期 45, 页码 14484-14509

出版社

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

关键词

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

资金

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

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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.

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