Stereoselectivity in the TiCl4-catalysed reaction of Danishefsky's diene with a N-(acyloxy)iminium ion: Synthesis of 5α versus 5β Δ1(2)-19-Nor-10-azasteroids. 4
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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3. A Concise Route to 19-Nor-10-azasteroids, a New Class of Steroid 5α-Reductase Inhibitors. 3.1 Synthesis of (+)-19-Nor-10-azatestosterone and (+)-17β-(Acetyloxy)-(5β)-10-azaestr-1-en-3-one
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1. ChemInform Abstract: Stereoselectivity in the TiCl4-Catalyzed Reaction of Danishefsky′s Diene with a N-(Acyloxy)iminium Ion: Synthesis of 5α versus 5β Δ1(2)-19-Nor-10-azasteroids. Part 4.;ChemInform;2010-06-18
2. Diels-Alder Reactions of Imino Dienophiles;Organic Reactions;2005-01-28
3. Selective non-steroidal inhibitors of 5α-reductase type 1;The Journal of Steroid Biochemistry and Molecular Biology;2004-01
4. Synthesis of 17β-N-Substituted 19-Nor-10-azasteroids as Inhibitors of Human 5α-Reductases I and II;Bioorganic & Medicinal Chemistry;2002-11
5. Novel inhibitors of 5α-reductase;Expert Opinion on Therapeutic Patents;2002-02
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