Search Results - "Kissick, Thomas P."
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Enzymatic Desymmetrization of Dimethyl Cylcohex-4-ene-cis-1,2-dicarboxylate to (1S,2R)-2-(Methoxycarbonyl)cyclohex-4-ene-1-carboxylic Acid
Published in Organic process research & development (15-05-2009)“…An efficient process for the synthesis of the monoester, (1S,2R)-2-(methoxycarbonyl)cyclohex-4-ene-1-carboxylic acid by Candida antarctica lipase (Novozym…”
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Process Research and Development for an Efficient Synthesis of the HIV Protease Inhibitor BMS-232632
Published in Organic process research & development (01-05-2002)“…Development of an efficient and scalable process for the human immunodeficiency virus (HIV) protease inhibitor BMS-232632…”
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Remarkable β-Selectivity in the Synthesis of β-1-C-Arylglucosides: Stereoselective Reduction of Acetyl-Protected Methyl 1-C-Arylglucosides without Acetoxy-Group Participation
Published in Journal of organic chemistry (07-12-2007)“…An efficient and practical process to generate β-C-arylglucoside derivatives was achieved. The process described involves Lewis acid mediated ionic reduction…”
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A Practical Asymmetric Synthesis of the Antiviral Agent Lobucavir, BMS-180194
Published in Organic process research & development (01-11-1998)“…A practical synthesis of the antiviral agent lobucavir, [1R-(1α,2β,3α)]-2-amino-9-[2,3-bis(hydroxymethyl)cyclobutyl]-6H-purin-6-one (BMS-180194), is described…”
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Conversion of L-pyroglutamic acid to 4-alkyl-substituted L-prolines. The synthesis of trans-4-cyclohexyl-L-proline
Published in Journal of organic chemistry (01-08-1986)Get full text
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Efficient Asymmetric Synthesis of the Vasopeptidase Inhibitor BMS-189921
Published in Organic letters (21-08-2003)“…An efficient asymmetric synthesis of the vasopeptidase inhibitor BMS-189921 was accomplished. Two short enantioselective syntheses of the common key…”
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Regioselective enzymatic aminoacylation of lobucavir to give an intermediate for lobucavir prodrug
Published in Bioorganic & medicinal chemistry (01-12-2000)“…Synthesis of lobucavir prodrug, L-valine, [(1 S,2 R,3 R)-3-(2-amino-1,6-dihydro-6-oxo-9 H-purin-9-yl)-2-(hydroxymethyl)cyclobutyl]methyl ester…”
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Confirmation of the structure of tetra- O-( tert-butyldimethylsilyl)- d-glucono-1,4-lactone formed by silylation of d-glucono-1,5-lactone
Published in Carbohydrate research (15-03-2002)“…The structure of tetra- O-( tert-butyldimethylsilyl)- d-glucono-1,4-lactone made by the silylation of d-glucono-1,5-lactone has been confirmed by…”
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Regioselective Activation of Aminothiazole(iminoxyacetic acid)acetic Acid: An Efficient Synthesis of the Monobactam Aztreonam
Published in Organic process research & development (01-11-2002)“…An efficient synthesis of the monobactam aztreonam…”
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Cupric bromide mediated oxidation of 4-carboxyoxazolines to the corresponding oxazoles
Published in Journal of organic chemistry (01-07-1993)Get full text
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Diastereoselective Reaction of a Grignard Reagent with Chiral Imides: A Practical Preparation of a Key Intermediate in the Synthesis of Ifetroban Sodium
Published in Organic process research & development (01-01-1997)“…A novel and highly efficient synthesis of [1S-(1α,2α,3α,4α)]-2-[[2-(3-methoxy-3-oxopropyl)phenyl]methyl]-7-oxabicyclo[2.2.1]heptane-3-carboxylic acid (A), a…”
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A Practical Asymmetric Synthesis of the Antiviral Agent Lobucavir, BMS-180194
Published in Organic process research & development (01-05-1999)Get full text
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1-Acyltriazoles as antiinflammatory agents
Published in Journal of medicinal chemistry (01-03-1982)“…Certain 1-acyl-3-phenyl-5-alkyltriazoles were synthesized and evaluated for antiinflammatory activity using the mouse active Arthus (MAA) reaction as the test…”
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The structures of alkoxycarbonyl, acyl, and sulfonate derivatives of 1-hydroxybenzotriazole: nitrogen- vs oxygen-substitution
Published in Journal of organic chemistry (01-01-1988)Get full text
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Synthesis of the triazolo[5,1-a][2,4]benzodiazepine ring system
Published in Journal of organic chemistry (01-01-1979)Get full text
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Synthesis and anti-MRSA Activity of Novel Cephalosporin Derivatives
Published in Tetrahedron (28-07-2000)“…Cephalosporin derivatives containing a unique combination of lipophilic C-7 sidechains and polar C-3 thiopyridinium groups were synthesized and found to…”
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A Practical Synthesis of an Anti-Methicillin Resistant Staphylococcus aureus Cephalosporin BMS-247243
Published in Organic process research & development (01-11-2000)“…A practical synthesis of the anti-methicillin resistant Staphylococcus aureus cephem…”
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Synthesis of a novel heterocyclic system: 2-oxo-1,3-dioxolo[4,5-c]pyridine-6-carboxylic acid, phenylmethyl ester
Published in Journal of heterocyclic chemistry (01-03-1989)“…The synthesis of heterobicyclic carbonate 4 and its conversions to the mixed carbonate 5 and carbamate 6 are described…”
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