Search Results - "Patel, Ramesh N"
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Biocatalysis for synthesis of pharmaceuticals
Published in Bioorganic & medicinal chemistry (01-04-2018)“…[Display omitted] Chirality is a key factor in the safety and efficacy of many drug products and thus the production of single enantiomers of drug…”
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2
Biocatalytic synthesis of chiral alcohols and amino acids for development of pharmaceuticals
Published in Biomolecules (02-10-2013)“…Chirality is a key factor in the safety and efficacy of many drug products and thus the production of single enantiomers of drug intermediates and drugs has…”
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Preparation of (R)-Amines from Racemic Amines with an (S)-Amine Transaminase from Bacillus megaterium
Published in Advanced synthesis & catalysis (09-06-2008)“…Screening was carried out to identify strains useful for the preparation of (R)‐1‐cyclopropylethylamine and (R)‐sec‐butylamine by resolution of the racemic…”
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4
Synthesis of chiral pharmaceutical intermediates by biocatalysis
Published in Coordination chemistry reviews (01-03-2008)“…Chirality is a key factor in the safety and efficacy of many drug products and thus the production of single enantiomers of drug intermediates has become…”
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5
Biocatalysis: Synthesis of Key Intermediates for Development of Pharmaceuticals
Published in ACS catalysis (02-09-2011)“…Chirality is a key factor for the safety and efficacy of many drug products. The production of single enantiomers of drug intermediates has become increasingly…”
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6
Microbial/enzymatic synthesis of chiral intermediates for pharmaceuticals
Published in Enzyme and microbial technology (01-11-2002)“…There has been an increasing awareness of the enormous potential of microorganisms and enzymes for the transformation of synthetic chemicals with high chemo-,…”
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7
Biocatalytic synthesis of intermediates for the synthesis of chiral drug substances
Published in Current Opinion in Biotechnology (01-12-2001)“…There has been an increasing awareness of the enormous potential of microorganisms and enzymes for the transformation of synthetic chemicals with high chemo-,…”
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Book Review Journal Article -
8
Enzymatic Synthesis of Chiral Intermediates for Drug Development
Published in Advanced synthesis & catalysis (01-08-2001)“…Chirality is a key factor in the efficacy of many drug products and thus the production of single enantiomers of drug intermediates has become increasingly…”
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9
Preparation of an Amino Acid Intermediate for the Dipeptidyl Peptidase IV Inhibitor, Saxagliptin, using a Modified Phenylalanine Dehydrogenase
Published in Advanced synthesis & catalysis (04-06-2007)“…The non‐proteinogenic amino acid 2‐(3‐hydroxy‐1‐adamantyl)‐(2S)‐aminoethanoic acid [2, (S)‐3‐hydroxyadamantylglycine], is a key intermediate required for the…”
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10
Biocatalytic Synthesis of Chiral Pharmaceutical Intermediates
Published in Food technology and biotechnology (01-10-2004)“…The production of single enantiomers of drug intermediates has become increasingly important in the pharmaceutical industry. Chiral intermediates and fine…”
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11
Hydroxylation of l-proline to cis-3-hydroxy- l-proline by recombinant Escherichia coli expressing a synthetic l-proline-3-hydroxylase gene
Published in Enzyme and microbial technology (01-12-2009)“…A synthetic gene encoding a Streptomyces l-proline-3-hydroxylase was constructed and used to produce the hydroxylase protein in recombinant Escherichia coli. A…”
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12
TOUR DE PACLITAXEL: Biocatalysis for Semisynthesis
Published in Annual review of microbiology (01-01-1998)“…In collaboration with the National Cancer Institute, Bristol-Myers Squibb has developed paclitaxel for treatment of various cancers; it has been approved by…”
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13
Enantioselective microbial reduction of substituted acetophenones
Published in Tetrahedron: asymmetry (19-04-2004)“…Graphic The chiral intermediate ( S)-1-(2′-bromo-4′-fluoro phenyl)ethanol 2 was prepared by the enantioselective microbial reduction of 2-bromo-4-fluoro…”
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14
Synthesis of ethyl-(3 R,5 S)-dihydroxy-6-benzyloxyhexanoates via diastereo- and enantioselective microbial reduction: Cloning and expression of ketoreductase III from Acinetobacter sp. SC 13874
Published in Enzyme and microbial technology (10-12-2008)“…Previously we have demonstrated the reduction of ethyl and t-butyl diketoesters 1 to the corresponding syn-(3 R,5 S)-dihydroxy esters 2a by Acinetobacter sp…”
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15
Enzymes for the removal of N-carbobenzyloxy protecting groups from N-carbobenzyloxy-d- and l-amino acids
Published in Journal of molecular catalysis. B, Enzymatic (01-01-2013)“…[Display omitted] ► Enzymes for the hydrolysis of N-carbobenzyloxy amino acids. ► Selective deprotection of N-CBz d- or l-amino acids. ► Enzymatic resolution…”
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Enzymatic Reduction of Adamantanones to Chiral Adamantanol Intermediates for the Synthesis of 11-β-Hydroxysteroid Dehydrogenase Inhibitors
Published in Organic process research & development (15-08-2014)“…An enzymatic reduction process was developed to convert the ketone 2-(6-oxo-2-phenyladamantan-2-yl)acetic acid to the chiral alcohol 2-((2S,…”
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17
Enzymatic Preparation of an (S)-Amino Acid from a Racemic Amino Acid
Published in Organic process research & development (21-01-2011)“…The (S)-amino acid, (S)-2-amino-3-(6-o-tolylpyridin-3-yl)propanoic acid (3), is a key intermediate needed for synthesis of an antidiabetic drug candidate…”
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18
Microbial transformation of 2-amino-4-methyl-3-nitropyridine
Published in Journal of industrial microbiology & biotechnology (01-12-2012)“…Biotransformation of the highly substituted pyridine derivative 2-amino-4-methyl-3-nitropyridine by Cunninghamella elegans ATCC 26269 yielded three products…”
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Purification and Cloning of a Ketoreductase used for the Preparation of Chiral Alcohols
Published in Advanced synthesis & catalysis (01-06-2005)“…The synthesis of the leading candidate compound in an anticancer program required (S)‐2‐chloro‐1‐(3‐chlorophenyl)‐ethanol as an intermediate. Other possible…”
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Enzymatic Preparation of a d-Amino Acid from a Racemic Amino Acid or Keto Acid
Published in Organic process research & development (21-11-2008)“…The d-amino acid (R)-2-amino-3-(7-methyl-1 H-indazol-5-yl)propanoic acid (3) is a key intermediate needed for synthesis of a drug candidate compound. Enzymatic…”
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