Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5263769 | Tetrahedron Letters | 2014 | 4 Pages |
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
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Authors
J.S. Yadav, N. Swapnil, M. Venkatesh, A.R. Prasad,