Chemistry - A European Journal · 2008 · 13 citations · 47 references
Natural SciencesChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistrySynthetic Medicinal ChemistryGonadal Steroid HormonesHeterocycle SynthesisHeterocyclic ChemistryOrganic SynthesisSteroid NomenclatureSteroid StructureChemical SubstituentsMulti-step SynthesisSteroid Core NomenclatureSteroid Hormone Analogs
A library of 17 novel estrogen analogues 3 and 4 containing different substituents at rings A and D (steroid nomenclature) was prepared in a five- to seven-step synthesis. The key transformation is a Sonogashira-coupling of cyclic vinyl iodides of type 7 or 8 with phenylacetylenes of type 9. Reduction of the keto function in 3 led to the estradiol analogue 5.
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Postmenopausal Hormone Therapy and Mortality
Francine Grodstein, Meir J. Stampfer, Graham A. Colditz et al. · New England Journal of Medicine · 1997 · 1.2K citations · Full text
John F. Couse, Jonathan Lindzey, Kaj Grandien et al. · Endocrinology · 1997 · 965 citations
Marvin J. Meyers, Jun Sun, Kathryn E. Carlson et al. · Journal of Medicinal Chemistry · 2001 · 678 citations · Full text