Improved Syntheses of 3,17β-Diacetoxyestra-1,3,5(10)-Trien-6-One
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397919608004657
Reference11 articles.
1. The Epimeric 6-Hydroxy-3,17β-estradiols
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3. Preparation of 17β-cestradiol-6-(0-carboxymethyl) oxime — bovine serum albumin conjugate
4. Syntheses of New Haptens for Radioimmunoassay of Estradiol
5. Potential steroidal antiestrogens
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1. Total Synthesis and Stereochemical Revision of the Chlorinated Sesquiterpene (±)-Gomerone C;Angewandte Chemie International Edition;2012-11-14
2. Total Synthesis and Stereochemical Revision of the Chlorinated Sesquiterpene (±)-Gomerone C;Angewandte Chemie;2012-11-14
3. ChemInform Abstract: Improved Syntheses of 3,17β-Diacetoxyestra-1,3,5(10)-trien-6-one.;ChemInform;2010-08-03
4. Total Synthesis of Guanacastepene A: A Route to Enantiomeric Control;The Journal of Organic Chemistry;2005-09-20
5. A Stereoselective Route to Guanacastepene A through a Surprising Epoxidation This work was supported by the National Institutes of Health (CA-28824). S.L. is a US Army breast cancer research program postdoctoral fellow (DAMD-17-99-1-9373). G.B.D. is an NIH postdoctoral fellow (1 F32 NS11150-01). D.S.T. is a Damon Runyon Cancer Research Foundation postdoctoral fellow (DRG-1641). We thank Dr. George Sukenick and Sylvi Rusli (NMR Core Facility, CA-02848) for mass spectral analyses.;Angewandte Chemie International Edition;2002-06-17
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