Article ID Journal Published Year Pages File Type
5265290 Tetrahedron Letters 2013 5 Pages PDF
Abstract
A concise, protection-free, and improved stereoselective total synthesis of ieodomycin A and ieodomycin B is described. The key steps involved in the synthesis are Evans aldol reaction and nucleophilic addition of potassium salt of mono methyl malonate.
Keywords
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Preview
Protection-free, short, and stereoselective synthesis of ieodomycin A and B
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