Platinum-catalyzed cycloisomerizations of a common enyne: a divergent entry to cyclopropane sesquiterpenoids. Formal synthesis of sarcandralactone A
Author:
Affiliation:
1. Department of Chemistry
2. Laboratory of Organic Chemistry
3. Aristotle University of Thessaloniki
4. Thessaloniki
5. Greece
Abstract
Highly selective metal-catalyzed cycloisomerizations of a 1,5-enyne allow the construction of either lindenane or myliol-type sesquiterpenoids.
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2016/OB/C6OB01226D
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5. Stereoselective Synthesis of 7,11-Guaien-8,12-olides from Santonin. Synthesis of Podoandin and (+)-Zedolactone A
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