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Volume 9, Issue 6
  • ISSN: 1570-1794
  • E-ISSN: 1875-6271

Abstract

This brief review deals with the recent progress in the implimentation of thio-Claisen rearrangement in synthetic organic chemistry. Thio-Claisen rearrangement has been utilized for the synthesis of many heterocyclic moieties of biological significance. Stereoselectivity of the thio-Claisen rearrangement has also been discussed. This short report mainly covers the literature published during 2003 onwards.

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/content/journals/cos/10.2174/157017912803901682
2012-12-01
2025-06-19

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  • Article Type:     Research Article
Keyword(s): 3]-sigmatropic shift; [3; [Rh2((S)-tbsp)4]; asymmetric rearrangement; catalyzed-Claisen rearrangement; cyclodextrin; dihydroflustramine C; electrocyclization; regioselective synthesis; sequential Claisen rearrangement; stereoselective synthesis; sulfur heterocycles; thermal Claisen-rearrangement; Thio-Claisen rearrangement

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