Search Results - "Bhatia, Gurpreet S"

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  1. 1

    Enantioselective Formal Total Synthesis of the Antitumor Macrolide Bryostatin 7 by Manaviazar, Soraya, Frigerio, Mark, Bhatia, Gurpreet S, Hummersone, Marc G, Aliev, Abil E, Hale, Karl J

    Published in Organic letters (28-09-2006)
    “…A new enantioselective synthesis of Masamune's AB fragment (1) for bryostatin 7 is described. Key steps in the new route include a Meerwein−Ponndorf−Verley…”
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  2. 2

    Enantioselective synthesis of (3 R)- and (3 S)-piperazic acids. The comparative unimportance of DMPU mediated retro-hydrazination by Hale, Karl J, Cai, Jiaqiang, Delisser, Vern, Manaviazar, Soraya, Peak, S.Andrew, Bhatia, Gurpreet S, Collins, Timothy C, Jogiya, Neha

    Published in Tetrahedron (01-01-1996)
    “…In response to a recent literature report by Decicco and Leathers (Ref. 13), the work of Hale, Delisser, and Manaviazar (1992) on the asymmetric synthesis of…”
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    Control of Olefin Geometry in the Bryostatin B-Ring through Exploitation of a C 2-Symmetry Breaking Tactic and a Smith−Tietze Coupling Reaction by Hale, Karl J, Hummersone, Marc G, Bhatia, Gurpreet S

    Published in Organic letters (27-07-2000)
    “…A completely stereocontrolled asymmetric synthesis of an advanced B-ring synthon for the bryostatin family of antitumor agents is reported. Noteworthy features…”
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  6. 6

    A mild protocol for the deoxygenation of α-hydrogen-containing sulfoxides to the corresponding sulfides by Bhatia, Gurpreet S., Graczyk, Piotr P.

    Published in Tetrahedron letters (28-06-2004)
    “…Graphic A mild method for the deoxygenation of α-hydrogen-containing sulfoxides to sulfides is reported. This synthetically useful and operationally simple…”
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    Generation of near-enantiopure α-alkyl α-formyl α-hydroxy ketones/esters and their interception with ethoxycarbonylmethylenetriphenylphosphorane by Bhatia, Gurpreet S., Lowe, Richard F., Stoodley, Richard J.

    Published in Tetrahedron letters (10-12-1998)
    “…Two protocols for the generation of the ( R)-enantiomers of α-alkyl α-formyl α-hydroxy ketones/esters in states of high enantiomeric purity are developed; the…”
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