Formal total synthesis of the myxobacteria metabolite apicularen A via a transannular oxy-Michael addition
Author:
Funder
Australian Research Council
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference45 articles.
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2. Myxobacteria: a source of new antibiotics
3. Critical variations of conjugational DNA transfer into secondary metabolite multiproducing Sorangium cellulosum strains So ce12 and So ce56: development of a mariner-based transposon mutagenesis system
4. A brief tour of myxobacterial secondary metabolism
5. Apicularens A and B, New Cytostatic Macrolides from Chondromyces Species (Myxobacteria): Production, Physico-chemical and Biological Properties.
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1. A synthetic study toward the core structure of (−)-apicularen A;Organic & Biomolecular Chemistry;2018
2. Design and synthesis of analogues of natural products;Organic & Biomolecular Chemistry;2015
3. Transannular reactions in asymmetric total synthesis;Tetrahedron;2014-12
4. 3.06 Transannular Electrophilic Cyclizations;Comprehensive Organic Synthesis II;2014
5. Gold(III) Chloride-Catalyzed 6-endo-trigOxa-Michael Addition Reactions for Diastereoselective Synthesis of Fused Tetrahydropyranones;Advanced Synthesis & Catalysis;2013-07-08
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