The absolute stereochemistry of the enzymic cyclisation to form the sterpurene sesquiterpenes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Chemoenzymatic Synthesis of the Enantiomer of 4,12-Dihydroxysterpurene, the Structure Assigned to a Metabolite Isolated from the Culture Broth of Stereum purpureum;Organic Letters;2014-12-18
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3. Mushroom Hunting by Using Bioinformatics: Application of a Predictive Framework Facilitates the Selective Identification of Sesquiterpene Synthases in Basidiomycota;ChemBioChem;2013-10-24
4. Protoilludane sesquiterpenes: synthesis of (±)-cerapicol, formal synthesis of (±)-sterpurene, and synthesis and absolute configuration of (+)-cerapicol;Tetrahedron;2009-01
5. Cycloaddition of Cyclohexa-2,4-dienones, Ring-Closing Metathesis, and Photochemical Reactions: A Common Stereoselective Approach to Duprezianane, Polyquinane and Sterpurane Frameworks;The Journal of Organic Chemistry;2007-02-21
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