Abstract
[reaction: see structure] A regioselective synthesis of 4-alkyl-1,3,5-triarylpyrazoles has been developed for the preparation of unsymmetrically substituted systems of interest as ligands for the estrogen receptor.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Isomerism
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Ligands
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Pyrazoles / chemical synthesis*
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Pyrazoles / metabolism
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Receptors, Estrogen / metabolism
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Selective Estrogen Receptor Modulators / chemical synthesis*
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Selective Estrogen Receptor Modulators / metabolism
Substances
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Ligands
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Pyrazoles
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Receptors, Estrogen
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Selective Estrogen Receptor Modulators