Journal article
Synthetic studies toward the construction of the cis-decalin portion of superstolides A and B. Application of a sequential double michael reaction and an anionic oxy-Cope rearrangement
Organic letters, Vol.7(10), pp.1939-1942
05/12/2005
DOI: 10.1021/ol050339w
PMID: 15876024
Abstract
A highly convergent strategy for the asymmetric synthesis of the cis-decalin portion of the antitumor macrolide superstolide A was developed. The key reactions in our approach involve a sequential double Michael reaction and an anionic oxy-Cope rearrangement.
Details
- Title: Subtitle
- Synthetic studies toward the construction of the cis-decalin portion of superstolides A and B. Application of a sequential double michael reaction and an anionic oxy-Cope rearrangement
- Creators
- Zhengmao Hua - University of IowaWensheng Yu - University of IowaMei Su - University of IowaZhendong Jin - University of Iowa
- Resource Type
- Journal article
- Publication Details
- Organic letters, Vol.7(10), pp.1939-1942
- DOI
- 10.1021/ol050339w
- PMID
- 15876024
- ISSN
- 1523-7060
- eISSN
- 1523-7052
- Language
- English
- Date published
- 05/12/2005
- Academic Unit
- Pharmaceutical Sciences and Experimental Therapeutics; Medicinal and Natural Products Chemistry
- Record Identifier
- 9984365896802771
Metrics
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