Conformational analysis of the 16-membered epoxyenone and complete stereoselection in the reduction of its C9 carbonyl group, the key reaction in the synthesis of maridonolides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. ChemInform Abstract: Chiral Synthesis of Polyketide Derived Natural Products. Part 37. Conformational Analysis of the 16-Membered Epoxyenone and Complete Stereoselection in the Reduction of Its C9 Carbonyl Group, the Key Reaction in the Synthesis of Marid;ChemInform;2010-08-21
2. Design and Synthesis of 16-Membered Hybrid Macrolide Having a Thiazole Side Chain on the Carbonolide Skeleton;HETEROCYCLES;2004
3. An Alternative and Facile Synthesis of Pikronolide;HETEROCYCLES;1997
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