Search Results - "Bhatia, Gurpreet S"
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Enantioselective Formal Total Synthesis of the Antitumor Macrolide Bryostatin 7
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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Enantioselective synthesis of (3 R)- and (3 S)-piperazic acids. The comparative unimportance of DMPU mediated retro-hydrazination
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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The neuroprotective action of JNK3 inhibitors based on the 6,7-dihydro-5H-pyrrolo[1,2-a]imidazole scaffold
Published in Bioorganic & medicinal chemistry letters (01-11-2005)“…Imidazole-based structures of p38 inhibitors served as a starting point for the design of JNK3 inhibitors. Construction of a…”
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Synthesis of A83586C Analogs with Potent Anticancer and β-Catenin/ TCF4/Osteopontin Inhibitory Effects and Insights Into How A83586C Modulates E2Fs and pRb
Published in Organic letters (05-02-2009)“…The synthesis of three potent new antitumor agents is described: the A83586C−citropeptin hybrid (1), the A83586C−GE3 hybrid (2), and l-Pro-A83586C (3)…”
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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
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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A mild protocol for the deoxygenation of α-hydrogen-containing sulfoxides to the corresponding sulfides
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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The neuroprotective action of JNK3 inhibitors based on the 6,7-dihydro-5 H-pyrrolo[1,2- a]imidazole scaffold
Published in Bioorganic & medicinal chemistry letters (2005)“…The synthesis and neuroprotective properties of three representative enantiomeric pairs ( S)- 2 and ( R)- 2 are reported. Imidazole-based structures of p38…”
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Generation of near-enantiopure α-alkyl α-formyl α-hydroxy ketones/esters and their interception with ethoxycarbonylmethylenetriphenylphosphorane
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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