Total Synthesis of (±)-Tremulenolide A and (±)-Tremulenediol A via a Stereoselective Cyclopropanation/Cope Rearrangement Annulation Strategy
Author:
Affiliation:
1. Department of Chemistry, State University of New York at Buffalo, Buffalo, New York 14260-3000
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo971577a
Reference15 articles.
1. The tremulanes, a new group of sesquiterpenes from the aspen rotting fungus Phellinus tremulae
2. Tandem cyclopropanation/cope rearrangement: a general method for the construction of seven-membered rings
3. An approach to the tremulane skeleton: Synthesis of (±)-8a-epi-tremulenolide B
4. New and efficient approach to functionalized hydroazulenes via 2-methylcyclopentenone 3-dimethylsulfoxonium methylide
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