1,721,139 research outputs found

    Ring Expansion of Thiochroman-4-one and Isothiochroman-4-one with Ethyl Diazo(lithio)acetate to Tetrahydro-benzothiepin-*-oxoesters

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    When thiochroman-4-one (1 ) and isothiochroman-4-one (3) were treated with ethyl diazo(lithio)acetate, ethyl 2,3-dihydro-4-hydroxy-1-benzothiepin-5-carboxylate (2) and ethyl 1,3-dihydro-4-hydroxy-2-benzothiepin-5- carboxylate (4), respectively, were formed. An improved procedure for the two-step addition-ring expansion sequence is described. The preparation of 2.3-dihydro-1 -benzothiepin-4(5H)-one (7) and of 1.3-dihydro-2- benzothiepin-4(5H)-one (8) from the esters (2) and (4), respectively, is reported. Deoxygenation of (7) and (8) to 2,3,4,5-tetrahydro-1 -benzothiepin (9) and 1,3,4,5-tetrahydro-2-benzothiepin (1 0) by Caglioti reduction is described

    Farnesoid x receptor modulators

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    The present application provides a compound of formula I or a pharmaceutically acceptable salt, solvate, or amino acid conjugate thereof

    O-Benzyl-(S)-Serine, a New Chiral Selector for Ligand-Exchange Chromatography of Amino Acids

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    O-Benzyl-(S)-serine is a new selector for chiral ligand-exchange chromatography which has proved to be effective in the analytical separation of some natural and unnatural underivatized amino acids with fair to good separation and resolution factors. Both chiral mobile phase (CMP) and hydrophobically coated chiral stationary phase (CSP) approaches were successfully employed. A not completely clarified mechanism of chiral recognition is discussed
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