Search Results - "Garigipati, Ravi"
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Identification of a novel, non-tetrahydroquinoline variant of the cholesteryl ester transfer protein (CETP) inhibitor torcetrapib, with improved aqueous solubility
Published in Xenobiotica (01-07-2014)“…Abstract 1. Elaborate studies of cholesteryl ester transfer protein (CETP) polymorphisms and genetic deficiency in humans suggest direct links between CETP,…”
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Novel solid-phase preparation of 2,6,9-trisubstituted purines for combinatorial library generation
Published in Tetrahedron letters (09-04-2001)Get full text
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Characterization of novel composites from polybenzoxazine and granite powder
Published in SN applied sciences (01-09-2020)“…The potential of using granite dust as reinforcement into polybenzoxazine matrix was investigated. In this article, novel granite powder waste-reinforced…”
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Use of Spin Echo Magic Angle Spinning (1)H NMR in Reaction Monitoring in Combinatorial Organic Synthesis
Published in Journal of organic chemistry (19-04-1996)Get full text
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1-Substituted 4-Aryl-5-pyridinylimidazoles: A New Class of Cytokine Suppressive Drugs with Low 5-Lipoxygenase and Cyclooxygenase Inhibitory Potency
Published in Journal of medicinal chemistry (27-09-1996)“…A series of 1-alkyl- or -aryl-4-aryl-5-pyridinylimidazoles (A) were prepared and tested for their ability to bind to a recently discovered protein kinase…”
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Regulation of stress-induced cytokine production by pyridinylimidazoles; inhibition of CSBP kinase
Published in Bioorganic & medicinal chemistry (01-01-1997)“…Members of three classes of pyridinylimidazoles bind with varying affinities to CSBP (p38) kinase which is a member of a stress-induced signal transduction…”
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Enantioselective Synthesis of 5-LO Inhibitor Hydroxyureas. Tandem Nucleophilic Addition−Intramolecular Cyclization of Chiral Nitrones
Published in Journal of organic chemistry (08-08-1997)“…An enantioselective synthesis of chiral hydroxyurea based 5-lipoxygenase inhibitors is reported via a five-step sequence in about 30% overall yield. The…”
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Use of Spin Echo Magic Angle Spinning 1H NMR in Reaction Monitoring in Combinatorial Organic Synthesis
Published in Journal of organic chemistry (19-04-1996)Get full text
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Process Development and Scale-Up of an Hsp90 Inhibitor
Published in Organic process research & development (16-11-2012)“…A scalable process for the manufacture of a Hsp90 inhibitor was developed and optimized. Key features in the seven-step process include a selective SNAr…”
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Stereospecific synthesis of acyclic unsaturated amino alcohols. A new approach to threo and erythro sphingosine
Published in Journal of the American Chemical Society (01-06-1983)Get full text
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Stereoselective total synthesis of the antitumor antibiotic (-)-bactobolin
Published in Journal of organic chemistry (01-08-1988)Get full text
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Total synthesis of (+)-actinobolin
Published in Journal of the American Chemical Society (01-12-1985)Get full text
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Development of a strategy for convergent total synthesis of the aureolic acid antitumor antibiotics
Published in Journal of organic chemistry (01-10-1982)Get full text
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Attempted synthesis of biotin
Published in Journal of organic chemistry (01-03-1988)Get full text
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Total synthesis of anhydrocannabisativene
Published in Journal of the American Chemical Society (01-05-1984)Get full text
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Reagents for combinatorial organic synthesis: preparation and uses of Rink-chloride
Published in Tetrahedron letters (29-09-1997)“…The preparation of Rink-chloride and its utility in attaching various nucleophiles to a solid support are described…”
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Pyrimidinylimidazole inhibitors of p38: cyclic N-1 imidazole substituents enhance p38 kinase inhibition and oral activity
Published in Bioorganic & medicinal chemistry letters (05-11-2001)“…Optimization of a series of N-1-cycloalkyl-4-aryl-5-(pyrimidin-4-yl)imidazole inhibitors of p38 kinase is reported. Oral administration of inhibitors…”
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Diastereoselective synthesis of unsaturated vicinal amino alcohols via Diels-Alder reactions of N-sulfinyl dienophiles
Published in Journal of the American Chemical Society (01-12-1984)Get full text
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