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AZD7545, a novel inhibitor of pyruvate dehydrogenase kinase 2 (PDHK2), activates pyruvate dehydrogenase in vivo and improves blood glucose control in obese (fa/fa) Zucker rats

Biochemical Society transactions, 2003-12, Vol.31 (Pt 6), p.1165-1167

2003

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AZD7545 is a selective inhibitor of pyruvate dehydrogenase kinase 2

Biochemical Society transactions, 2003-12, Vol.31 (Pt 6), p.1168-1170

2003

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Phenoxypropylamines: A New Series of Squalene Synthase Inhibitors

Journal of medicinal chemistry, 1995-10, Vol.38 (21), p.4157-4160

1995

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New Non-Peptide Endothelin-A Receptor Antagonists: Synthesis, Biological Properties, and Structure−Activity Relationships of 5-(Dimethylamino)-N-pyridyl-, -N-pyrimidinyl-, -N-pyridazinyl-, and -N-pyrazinyl-1-naphthalenesulfonamides

Journal of medicinal chemistry, 1997-03, Vol.40 (6), p.996-1004

1997

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Total synthesis of (.+-.)-byssochlamic acid

Journal of the American Chemical Society, 1992-11, Vol.114 (24), p.9673-9674

1992

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Template-directed phenolic oxidative coupling. A stereocontrolled route to spiro dienones

Journal of the American Chemical Society, 1990-11, Vol.112 (23), p.8595-8596

1990

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Synthesis of ethynylazaspirocycloundecene: approach to side chain unsaturated histrionicotoxins

Tetrahedron letters, 1988, Vol.29 (24), p.2989-2992

1988

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Recoverable chiral sulfoxides for asymmetric synthesis: preparation, regeneration and application to the asymmetric aldol reaction

Journal of the Chemical Society, Perkin Transactions 1, 1993 (14), p.1581

1993

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Dependence of ring closure stereoselectivity on the nature of the leaving group: application to the synthesis of a new class of chiral sulfoxide for the control of asymmetric aldol reactions

Journal of the Chemical Society, Perkin Transactions 1, 1991 (12), p.3383

1991

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A new class of recoverable chiral sulphoxide: Application to the asymmetric synthesis of β-hydroxy esters

Tetrahedron letters, 1992-09, Vol.33 (37), p.5427-5430

1992

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The asymmetric synthesis of allylic alcohols using a recoverable chiral sulphoxide

Tetrahedron letters, 1994-03, Vol.35 (11), p.1785-1788

1994

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N-methyl-2-[4-(2-methylpropyl)phenyl]-3-(3-methoxy-5-methylpyrazin-2-ylsulfamoyl)benzamide ; One of a class of novel benzenesulphonamides which are orally-active, ETA-Selective endothelin antagonists

Bioorganic & medicinal chemistry letters, 1997-06, Vol.7 (11), p.1399-1402

1997

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New non-peptide endothelin-A receptor antagonists: Synthesis, biological properties, and structure-activity relationships of 5-(dimethylamino)-N-pyridyl-, -N-pyrimidinyl-, -N-pyridazinyl-, and -N-pyrazinyl-l-naphthalenesulfonamides

Journal of medicinal chemistry, 1997, Vol.40 (6), p.996-1004

1997

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Studies towards the synthesis of histrionicotoxin and other ion-channel blockers

Butlin, R J

1986

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Recoverable chiral sulfoxides for asymmetric synthesis: application to stereoselective carbonyl reduction and the asymmetric synthesis of allylic alcohols

Journal of the Chemical Society, Perkin Transactions 1, 1996-01 (1), p.95

1996

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Interpreting the genomic landscape of speciation: a road map for finding barriers to gene flow

Journal of evolutionary biology, 2017-08, Vol.30 (8), p.1450-1477

2017

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ChemInform Abstract: The Asymmetric Synthesis of Allylic Alcohols Using a Recoverable Chiral Sulfoxide

ChemInform, 1994-08, Vol.25 (34), p.no-no

1994

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ChemInform Abstract: Total Synthesis of (.+-.)-Byssochlamic Acid

ChemInform, 1993-04, Vol.24 (14), p.no-no

1993

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ChemInform Abstract: A New Class of Recoverable Chiral Sulfoxide: Application to the Asymmetric Synthesis of β-Hydroxy Esters

ChemInform, 1993-01, Vol.24 (4), p.no-no

1993

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Optimal controls for markov chains with restricted stata observations

Butlin, C R. J

1982

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Hybridization and speciation

Journal of evolutionary biology, 2013-02, Vol.26 (2), p.229-246

2013

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ChemInform Abstract: Recoverable Chiral Sulfoxides for Asymmetric Synthesis: Application to Stereoselective Carbonyl Reduction and the Asymmetric Synthesis of Allylic Alcohols

ChemInform, 1996-05, Vol.27 (19), p.no-no

1996

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ChemInform Abstract: Synthesis of Ethynylazaspirocycloundecene: Approach to Side Chain Unsaturated Histrionicotoxins

ChemInform, 1988-11, Vol.19 (48), p.no-no

1988

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ChemInform Abstract: Dependence of Ring Closure Stereoselectivity on the Nature of the Leaving Group: Application to the Synthesis of a New Class of Chiral Sulfoxide for the Control of Asymmetric Aldol Reactions

ChemInform, 1992-03, Vol.23 (13), p.no-no

1992

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Do the same genes underlie parallel phenotypic divergence in different Littorina saxatilis populations?

Molecular ecology, 2014-09, Vol.23 (18), p.4603-4616

2014

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AZD7545, a novel inhibitor of pyruvate dehydrogenase kinase 2 (PDHK2), activates pyruvate dehydrogenase in vivo and improves blood glucose control in obese (fa/fa) Zucker rats

AZD7545 is a selective inhibitor of pyruvate dehydrogenase kinase 2

Phenoxypropylamines: A New Series of Squalene Synthase Inhibitors

New Non-Peptide Endothelin-A Receptor Antagonists: Synthesis, Biological Properties, and Structure−Activity Relationships of 5-(Dimethylamino)-N-pyridyl-, -N-pyrimidinyl-, -N-pyridazinyl-, and -N-pyrazinyl-1-naphthalenesulfonamides

Total synthesis of (.+-.)-byssochlamic acid

Template-directed phenolic oxidative coupling. A stereocontrolled route to spiro dienones

Synthesis of ethynylazaspirocycloundecene: approach to side chain unsaturated histrionicotoxins

Recoverable chiral sulfoxides for asymmetric synthesis: preparation, regeneration and application to the asymmetric aldol reaction

Dependence of ring closure stereoselectivity on the nature of the leaving group: application to the synthesis of a new class of chiral sulfoxide for the control of asymmetric aldol reactions

A new class of recoverable chiral sulphoxide: Application to the asymmetric synthesis of β-hydroxy esters

The asymmetric synthesis of allylic alcohols using a recoverable chiral sulphoxide

N-methyl-2-[4-(2-methylpropyl)phenyl]-3-(3-methoxy-5-methylpyrazin-2-ylsulfamoyl)benzamide ; One of a class of novel benzenesulphonamides which are orally-active, ETA-Selective endothelin antagonists

New non-peptide endothelin-A receptor antagonists: Synthesis, biological properties, and structure-activity relationships of 5-(dimethylamino)-N-pyridyl-, -N-pyrimidinyl-, -N-pyridazinyl-, and -N-pyrazinyl-l-naphthalenesulfonamides

Studies towards the synthesis of histrionicotoxin and other ion-channel blockers

Recoverable chiral sulfoxides for asymmetric synthesis: application to stereoselective carbonyl reduction and the asymmetric synthesis of allylic alcohols

Interpreting the genomic landscape of speciation: a road map for finding barriers to gene flow

ChemInform Abstract: The Asymmetric Synthesis of Allylic Alcohols Using a Recoverable Chiral Sulfoxide

ChemInform Abstract: Total Synthesis of (.+-.)-Byssochlamic Acid

ChemInform Abstract: A New Class of Recoverable Chiral Sulfoxide: Application to the Asymmetric Synthesis of β-Hydroxy Esters

Optimal controls for markov chains with restricted stata observations

Hybridization and speciation

ChemInform Abstract: Recoverable Chiral Sulfoxides for Asymmetric Synthesis: Application to Stereoselective Carbonyl Reduction and the Asymmetric Synthesis of Allylic Alcohols

ChemInform Abstract: Synthesis of Ethynylazaspirocycloundecene: Approach to Side Chain Unsaturated Histrionicotoxins

ChemInform Abstract: Dependence of Ring Closure Stereoselectivity on the Nature of the Leaving Group: Application to the Synthesis of a New Class of Chiral Sulfoxide for the Control of Asymmetric Aldol Reactions

Do the same genes underlie parallel phenotypic divergence in different Littorina saxatilis populations?

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