Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5268129 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
As part of an approach to the synthesis of the antitubercular agent elisapterosin B, we prepared two different chiral, non-racemic olefinic substrates and examined their diastereoselective ring closure using mercury salts. The effort yielded potential precursors to elisapterosin B in good yield with good to excellent diastereocontrol.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Weijiang Ying, Charles L. Barnes, Michael Harmata,