An improved synthesis of 16β-hydroxy dehydroepiandrosterone
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Biochemistry
Reference4 articles.
1. The Action of Lead Tetraacetate on an Enol Acetate. The Epimeric 16-Acetoxy Derivatives of Epiandrosterone Acetate, their Interconversion and Rearrangement
2. Rearrangements of Steroidal Ring D Ketols1
3. The preparation of 16β-hydroxydehydroepiandrosterone using enzymic deacetylation
4. The identification and measurement of a new steroid 16β-hydroxydehydroepiandrosterone in infant urine
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1. Mechanistic aspects of rearrangement of 16α-hydroxy-17-keto steroids to the 17β-hydroxy-16-keto isomers;Steroids;2008-09
2. Production of 16β-(acetoxy)acetoxy derivatives by reaction of 17-keto steroid enol acetates with lead (IV) acetate;Steroids;2001-10
3. Lipase-Catalysed Regioselective Deacetylation of androstane derivatives;Helvetica Chimica Acta;1996-06-26
4. A time-dependent inactivation of aromatase by 19-substituted androst-4-ene-3,6,17-triones;Steroids;1993-01
5. Carbon-13 nuclear magnetic resonance spectral data of steroidal vicinal ketols and related compounds;Steroids;1991-04
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