Estrogen Receptor Ligands. 12. Synthesis of the Major Metabolites of an ERα-Selective, Dihydrobenzoxathiin Antagonist for Osteoporosis
Author:
Affiliation:
1. Departments of Medicinal Chemistry and Drug Metabolism, Merck Research Laboratories, P.O. Box 2000 (800B-109), Rahway, New Jersey 07065
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol047741f
Reference19 articles.
1. Dehydrative Reduction: A Highly Diastereoselective Synthesis of syn-Bisaryl(or Heteroaryl) Dihydrobenzoxathiins and Benzodioxane
2. Estrogen Receptor Ligands. II. Discovery of Benzoxathiins as Potent, Selective Estrogen Receptor α Modulators
3. Estrogen receptor ligands. Part 4: The SAR of the syn-dihydrobenzoxathiin SERAMs
4. Estrogen receptor ligands. Part 3: The SAR of dihydrobenzoxathiin SERMs
5. Asymmetric Catalysis Special Feature Part II: An efficient asymmetric synthesis of an estrogen receptor modulator by sulfoxide-directed borane reduction
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