| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2028861 | Steroids | 2008 | 4 Pages |
Abstract
A highly selective method to protect the 11β-OH position of steroid (1) has been developed. This is achieved via double silyl protection of the 11β, 17α-diol, followed by selective desilylation of the 17α-OH under basic conditions without the need for a fluoride source.
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Biochemistry
Authors
Paul A. Glossop, Marcel Hoogenraad, Torren M. Peakman, Dannielle F. Roberts,