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Gold-catalyzed tandem [3,3]-propargyl ester rearrangement leading to (E)-1H-inden-1-ones.

Authors :
Wang LJ
Zhu HT
Wang AQ
Qiu YF
Liu XY
Liang YM
Source :
The Journal of organic chemistry [J Org Chem] 2014 Jan 03; Vol. 79 (1), pp. 204-12. Date of Electronic Publication: 2013 Dec 19.
Publication Year :
2014

Abstract

An efficient method for the synthesis of (E)-1H-inden-1-ones using gold-catalyzed tandem [3,3]-propargyl ester rearrangement followed by Michael addition under mild reaction conditions has been developed. The resulting products are important frameworks found in numerous natural products and pharmaceutically active compounds, as well as being valuable intermediates in organic synthesis.

Details

Language :
English
ISSN :
1520-6904
Volume :
79
Issue :
1
Database :
MEDLINE
Journal :
The Journal of organic chemistry
Publication Type :
Academic Journal
Accession number :
24328090
Full Text :
https://doi.org/10.1021/jo402396h