An Electrochemical Approach to the Guanacastepenes
Author:
Affiliation:
1. Center for New Directions in Organic Synthesis, Department of Chemistry, University of California-Berkeley, Berkeley, California 94720
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol047387l
Reference52 articles.
1. A novel extension of the Stork–Jung vinylsilane Robinson annelation procedure for the introduction of the cyclohexene of guanacastepene
2. Synthesis of the Hydroazulene Ring System of Guanacastepene
3. Formal Synthesis of (±)-Guanacastepene A
4. Stereoselective synthesis of the bicyclo[5.3.0]decane portion of the diterpene antibiotic guanacastepene using a pyrylium-ylide [5+2] cycloaddition reaction
5. Synthesis of the hydroazulene portion of guanacastepene A using a [2.3]sigmatropic sulfoxide rearrangement: observations on silyl enol ether electrophilic chemistry for the introduction of the C-13 hydroxyl group
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