| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5277550 | Tetrahedron Letters | 2006 | 5 Pages |
Abstract
The ouabain isomers 1, 6, 20, 21, and 22 have been synthesized and shown to be readily separable by HPLC, which indicates that they do not correspond to a putative endogenous ouabain-like cardioregulator. 11-epi-Ouabain (1) is of interest as a safer alternative to ouabain.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Bor-Cherng Hong, Seongkon Kim, Tae-Seong Kim, E.J. Corey,