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