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New developments in the Peterson olefination reaction

Chemical Society reviews, 2002-05, Vol.31 (3), p.195-200

2002

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Asymmetric homogeneous hydrogenations at scale

Chemical Society reviews, 2012, Vol.41 (8), p.3340

2012

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Asymmetric homogeneous hydrogenations at scale

Chemical Society reviews, 2012-04, Vol.41 (8), p.334-338

2012

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An Epoxidation Approach to a Chiral Lactone: Application of the Shi Epoxidation

Organic process research & development, 2007-01, Vol.11 (1), p.44-51

2007

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Reductions of Aromatic Amino Acids and Derivatives

Organic process research & development, 2003-03, Vol.7 (2), p.164-167

2003

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Amine–boranes: effective reducing agents for the deracemisation of dl-amino acids using l-amino acid oxidase from Proteus myxofaciens

Tetrahedron letters, 2002-01, Vol.43 (4), p.707-710

2002

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Commercial, Synthetic Nonnutritive Sweeteners

Angewandte Chemie (International ed.), 1998-08, Vol.37 (13-14), p.1802-1817

1998

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Asymmetric Hydrogenation of Ketones Catalyzed by RuII-bicp Complexes

Angewandte Chemie (International ed.), 2004-05, Vol.43 (21), p.2816-2819

2004

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Novel biosynthetic routes to non-proteinogenic amino acids as chiral pharmaceutical intermediates

Journal of molecular catalysis. B, Enzymatic, 2001-01, Vol.11 (4-6), p.199-205

2001

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ChemInform Abstract: Popular Synthetic Approaches to Pharmaceuticals

ChemInform, 2015-05, Vol.46 (21), p.no-no

Ager, David J.

2015

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The Synthesis of the High-Potency Sweetener, NC-00637. Part 2: Preparation of the Pyridine Moiety

Organic process research & development, 2004-01, Vol.8 (1), p.62-71

2004

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The Synthesis of the High-Potency Sweetener, NC-00637. Part 3: The Glutamyl Moiety and Coupling Reactions

Organic process research & development, 2004-01, Vol.8 (1), p.72-85

2004

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The Synthesis of the High-Potency Sweetener, NC-00637. Part 1: The Synthesis of (S)-2-Methylhexanoic Acid

Organic process research & development, 2003-05, Vol.7 (3), p.369-378

2003

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Asymmetric Hydrogenation of Ketones Catalyzed by Ru II –bicp Complexes

Angewandte Chemie International Edition, 2004-05, Vol.43 (21), p.2816-2819

2004

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Synthesis of Unnatural/Nonproteinogenic α‐Amino Acids

Amino Acids, Peptides and Proteins in Organic Chemistry, 2009, p.495-526

2009

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Pig Liver Esterase Catalyzed Hydrolyses of Diesters. A New Route to the Syntheses of Achiral Half-Esters

Synthetic communications, 1995-03, Vol.25 (5), p.739-742

1995

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Simple and Efficient N-Acylation Reactions of Chiral Oxazolidine Auxiliaries

Synthesis (Stuttgart), 1996-11, Vol.1996 (11), p.1283-1285

1996

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Silicon-containing carbonyl equivalents

Chemical Society reviews, 1982, Vol.11 (4), p.493

Ager, David J.

1982

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Reductions of 1,3-dicarbonyl systems with ruthenium-biarylbisphosphine catalysts

Tetrahedron: asymmetry, 1997-10, Vol.8 (20), p.3327-3355

1997

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Cinchona Alkaloids as Chiral Ligands in Asymmetric Oxidations

Cinchona Alkaloids in Synthesis and Catalysis, 2009, p.29-71

2009

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A detailed study of the diastereoselective catalytic hydrogenation of 6-hydroxytetrahydroisoquinoline-(3R)-carboxylic ester intermediatesElectronic supplementary information (ESI) available: Synthesis of substrates, analytical methods, hydrogenation procedures, details of kinetic model. See DOI: 10.1039/c2cy20251d

2012-09

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Route and Process Selection

Process Understanding, 2011, p.17-58

2011

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ChemInform Abstract: Asymmetric Homogeneous Hydrogenations at Scale

ChemInform, 2012-07, Vol.43 (30), p.no-no

2012

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Copper-Catalyzed Coupling for a Green Process

Transition Metal-Catalyzed Couplings in Process Chemistry, 2013, p.1-13

2013

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A detailed study of the diastereoselective catalytic hydrogenation of 6-hydroxytetrahydroisoquinoline-(3R)-carboxylic ester intermediates

Catalysis science & technology, 2012-01, Vol.2 (10), p.2077

2012

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New developments in the Peterson olefination reaction

Asymmetric homogeneous hydrogenations at scale

Asymmetric homogeneous hydrogenations at scale

An Epoxidation Approach to a Chiral Lactone: Application of the Shi Epoxidation

Reductions of Aromatic Amino Acids and Derivatives

Amine–boranes: effective reducing agents for the deracemisation of dl-amino acids using l-amino acid oxidase from Proteus myxofaciens

Commercial, Synthetic Nonnutritive Sweeteners

Asymmetric Hydrogenation of Ketones Catalyzed by RuII-bicp Complexes

Novel biosynthetic routes to non-proteinogenic amino acids as chiral pharmaceutical intermediates

ChemInform Abstract: Popular Synthetic Approaches to Pharmaceuticals

The Synthesis of the High-Potency Sweetener, NC-00637. Part 2: Preparation of the Pyridine Moiety

The Synthesis of the High-Potency Sweetener, NC-00637. Part 3: The Glutamyl Moiety and Coupling Reactions

The Synthesis of the High-Potency Sweetener, NC-00637. Part 1: The Synthesis of (S)-2-Methylhexanoic Acid

Asymmetric Hydrogenation of Ketones Catalyzed by Ru II –bicp Complexes

Synthesis of Unnatural/Nonproteinogenic α‐Amino Acids

Pig Liver Esterase Catalyzed Hydrolyses of Diesters. A New Route to the Syntheses of Achiral Half-Esters

Simple and Efficient N-Acylation Reactions of Chiral Oxazolidine Auxiliaries

Silicon-containing carbonyl equivalents

Reductions of 1,3-dicarbonyl systems with ruthenium-biarylbisphosphine catalysts

Cinchona Alkaloids as Chiral Ligands in Asymmetric Oxidations

Route and Process Selection

ChemInform Abstract: Asymmetric Homogeneous Hydrogenations at Scale

Copper-Catalyzed Coupling for a Green Process

A detailed study of the diastereoselective catalytic hydrogenation of 6-hydroxytetrahydroisoquinoline-(3R)-carboxylic ester intermediates

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