Article ID Journal Published Year Pages File Type
5263769 Tetrahedron Letters 2014 4 Pages PDF
Abstract
Stereoselective synthesis of the C21-C40 core segment of caylobolide A has been achieved following a highly efficient convergent strategy. The key reactions featured in the synthesis are Prins cyclization, reductive radical cyclization, Sharpless asymmetric epoxidation and olefin cross metathesis.
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Authors
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