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Design of a Highly Selective and Potent Class of Non‐planar Estrogen Receptor β Agonists.

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TLDR
This describes the syntheses of various dibenz ofurans and cycloheptanobenzofurans as estrogen receptor β agonists.
Abstract
This describes the syntheses of various dibenzofurans and cycloheptanobenzofurans as estrogen receptor β agonists.

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Versatility or Promiscuity: The Estrogen Receptors, Control of Ligand Selectivity and an Update on Subtype Selective Ligands

TL;DR: How nature controls ER specificity and how the subtle differences in receptor subtypes are exploited in pharmaceutical design to achieve binding specificity and subtype selectivity for desired biological response are discussed.
Journal ArticleDOI

Catalytic Enantioselective Pinacol and Meinwald Rearrangements for the Construction of Quaternary Stereocenters.

TL;DR: Chiral N-triflyl phosphoramide-catalyzed enantioselective pinacol rearrangement of 1,2-tertiary diols and mechanistically related Meinwald rearrangements of tetrasubstituted epoxides for the synthe-sis of enantioenriched 2-alkynyl-2-arylcyclohexanones and 2,2 -diarylcyclo hexanones are reported.
References
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Journal ArticleDOI

Design of a highly selective and potent class of non-planar estrogen receptor β agonists.

TL;DR: A new class of dihydrobenzofurans as potent and selective ERβ agonists and compound trans‐10‐SS appears to be the first molecule to take advantage of both conservative amino acid differences found in the α‐ and β‐faces of the binding cavities of ERα and ERβ.
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