Highly Diastereoselective Formation of Spirocyclic Compounds via 1,5-Hydrogen Transfer: A Total Synthesis of (−)-Erythrodiene
Author:
Affiliation:
1. Departement für Chemie und Biochemie, Universität Bern, Freiestrasse 3, 3012 Bern, Switzerland
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol051426r
Reference12 articles.
1. Spirojatamol, a new skeletal sesquiterpenoid of roots
2. Erythrodiene: A new spirobicyclic sesquiterpene of a rare skeletal class from the caribbean gorgonian coral Erythropodium caribaeorum
3. Enantiospecific synthesis of (+)-dihydroerythrodiene, (+)-dihydrospirojatamol and (+)-dihydroepispirojatamol
4. Facile construction of spirobicyclic skeletons by intramolecular aldol reaction: simple formal syntheses of (±)-spirojatamol and (±)-erythrodiene
5. Anti Selective Spirocarbomercuration: Synthesis and Stereochemistry of the Spirobicyclic Sesquiterpenes Spirojatamol and Erythrodiene
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