Side-Chain Introduction In 16β-Acetoxy-17-oxo-androstanes
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397919008051534
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4. 13C NMR spectroscopic study of the rearrangement of 16β-hydroxy-17-oxo steroids to 17β-hydroxy-16-oxo isomers
5. Dissimilar behaviour of 3?, 16?-dihydroxy-5?-androstan-17-one Diacetate under Basic and Acidic Conditions
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1. ChemInform Abstract: Side-Chain Introduction in 16β-Acetoxy-17-oxoandrostanes.;ChemInform;2010-08-23
2. OSW Saponins: Facile Synthesis toward a New Type of Structures with Potent Antitumor Activities;The Journal of Organic Chemistry;2005-11-05
3. 23-Oxa-Analogues of OSW-1: Efficient Synthesis and Extremely Potent Antitumor Activity;Angewandte Chemie International Edition;2004-08-20
4. Mechanistic studies of the rearrangements of steroidal 16,17-ketols and syntheses of 20→16-cis-γ-carbolactones;Bioorganic & Medicinal Chemistry;1999-05
5. Stereospecific Synthesis of Steroidal 20,16-γ-Carbolactones;Synthetic Communications;1998-11
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