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Towards control of χ-space: Conformationally constrained analogues of Phe, Tyr, Trp and His

Tetrahedron, 1999-01, Vol.55 (3), p.585-615

1999

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Nonpeptide Cholecystokinin-2 Receptor Agonists

Journal of medicinal chemistry, 2001-04, Vol.44 (8), p.1125-1133

2001

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Non-Peptide Cholecystokinin-B/Gastrin Receptor Antagonists Based on Bicyclic, Heteroaromatic Skeletons

Journal of medicinal chemistry, 1996-04, Vol.39 (9), p.1806-1815

1996

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Synthesis of Cyclic Sulfonamides through Intramolecular Diels−Alder Reactions

Organic letters, 2001-02, Vol.3 (3), p.369-371

2001

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Improving the Affinity and Selectivity of a Nonpeptide Series of Cholecystokinin-B/Gastrin Receptor Antagonists Based on the Dibenzobicyclo[2.2.2]octane Skeleton

Journal of medicinal chemistry, 1995-10, Vol.38 (21), p.4294-4302

1995

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2,7-Dioxo-2,3,4,5,6,7-hexahydro-1H-benzo[h][1,4]diazonine as a New Template for the Design of CCK2 Receptor Antagonists

Journal of medicinal chemistry, 2000-09, Vol.43 (19), p.3518-3529

2000

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From histamine to imidazolylalkyl-sulfonamides : The design of a novel series of histamine H3-RECEPTOR antagonists

Bioorganic & medicinal chemistry letters, 1999-07, Vol.9 (13), p.1825-1830

1999

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Methods for the synthesis of gem-difluoromethylene compounds

Tetrahedron, 1996-06, Vol.52 (26), p.8619-8683

1996

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A convenient strategy for replacement of the anomeric hydroxyl group by difluoromethyl functionality in carbohydrate derivatives

Tetrahedron, 1993-09, Vol.49 (36), p.8087-8106

1993

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INCORPORATION OF CONFORMATIONALLY CONSTRAINED PHENYLALANINE DERIVATIVES TIC, SIC, HIC AND NIC INTO A CHOLECYSTOKININ-B/GASTRIN RECEPTOR ANTAGONIST

Bioorganic & medicinal chemistry letters, 1997-05, Vol.7 (10), p.1289-1292

1997

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trans-3-Benzoyl-2-tert-butyl-4-isobutyl-1,3-oxazolidin-5-one

Acta crystallographica. Section C, Crystal structure communications, 1991-11, Vol.47 (11), p.2276-2277

1991

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The iodination and iodocyclisation of some alkenylmalonates

Tetrahedron letters, 1992-08, Vol.33 (34), p.4975-4978

1992

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Identification of an Asymmetric Pauson−Khand Precatalyst

Organometallics, 2003-12, Vol.22 (26), p.5382-5384

2003

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Histamine H3 receptor antagonists

Expert opinion on therapeutic patents, 2000-07, Vol.10 (7), p.1045-1055

2000

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Optimization of the in Vitro and in Vivo Properties of a Novel Series of 2,4,5-Trisubstituted Imidazoles as Potent Cholecystokinin-2 (CCK2) Antagonists

Journal of medicinal chemistry, 2005-11, Vol.48 (22), p.6803-6812

2005

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New routes to beta-cycloalkylalanine derivatives using serine-derived organozinc reagents

Organic & biomolecular chemistry, 2005-11, Vol.3 (22), p.4117-4123

2005

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Pilot study of immunological factors in non-inflammatory bowel disease enterocutaneous fistulas

International journal of surgery (London, England), 2017-05, Vol.41, p.127-133

2017

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CCK2 receptor antagonists containing the conformationally constrained phenylalanine derivatives, including the new amino acid Xic

European journal of medicinal chemistry, 2002-05, Vol.37 (5), p.379-389

2002

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Synthesis of meta- and paracyclophanes containing unsaturated amino acid residues

Tetrahedron, 2004-08, Vol.60 (32), p.6945-6958

2004

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4-Chlorobenzyl sulfonamide and sulfamide derivatives of histamine homologues: the design of potent histamine H3 receptor antagonists

Bioorganic & medicinal chemistry letters, 1999-11, Vol.9 (21), p.3103-3108

1999

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An Efficient Synthesis of (2S) and (2R)-N-Benzoyl-2-t-butyl-4-methyleneoxazolidin-5-one

Australian journal of chemistry, 1993, Vol.46 (9), p.1425

1993

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Histamine H 3 receptor antagonists

Expert opinion on therapeutic patents, 2000-07, Vol.10 (7), p.1045-1055

2000

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Application of 7-endo, 8-endo and 9-endo radical cyclisations to the synthesis of conformationally constrained amino acids and comparison with the corresponding Heck reactions

Chemical communications (Cambridge, England), 1997 (6), p.637-638

1997

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Synthesis and structural analysis of dehydrophenylalanine cyclophanes

Chemical communications (Cambridge, England), 2002-01 (17), p.1938-1939

2002

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2,7-Dioxo-2,3,4,5,6,7-hexahydro-1H-benzo[h][1,4]diazonine as a new template for the design of CCK(2) receptor antagonists

Journal of medicinal chemistry, 2000-09, Vol.43 (19), p.3518-3529

2000

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Towards control of χ-space: Conformationally constrained analogues of Phe, Tyr, Trp and His

Nonpeptide Cholecystokinin-2 Receptor Agonists

Non-Peptide Cholecystokinin-B/Gastrin Receptor Antagonists Based on Bicyclic, Heteroaromatic Skeletons

Synthesis of Cyclic Sulfonamides through Intramolecular Diels−Alder Reactions

Improving the Affinity and Selectivity of a Nonpeptide Series of Cholecystokinin-B/Gastrin Receptor Antagonists Based on the Dibenzobicyclo[2.2.2]octane Skeleton

2,7-Dioxo-2,3,4,5,6,7-hexahydro-1H-benzo[h][1,4]diazonine as a New Template for the Design of CCK2 Receptor Antagonists

From histamine to imidazolylalkyl-sulfonamides : The design of a novel series of histamine H3-RECEPTOR antagonists

Methods for the synthesis of gem-difluoromethylene compounds

A convenient strategy for replacement of the anomeric hydroxyl group by difluoromethyl functionality in carbohydrate derivatives

INCORPORATION OF CONFORMATIONALLY CONSTRAINED PHENYLALANINE DERIVATIVES TIC, SIC, HIC AND NIC INTO A CHOLECYSTOKININ-B/GASTRIN RECEPTOR ANTAGONIST

trans-3-Benzoyl-2-tert-butyl-4-isobutyl-1,3-oxazolidin-5-one

The iodination and iodocyclisation of some alkenylmalonates

Identification of an Asymmetric Pauson−Khand Precatalyst

Histamine H3 receptor antagonists

Optimization of the in Vitro and in Vivo Properties of a Novel Series of 2,4,5-Trisubstituted Imidazoles as Potent Cholecystokinin-2 (CCK2) Antagonists

New routes to beta-cycloalkylalanine derivatives using serine-derived organozinc reagents

Pilot study of immunological factors in non-inflammatory bowel disease enterocutaneous fistulas

CCK2 receptor antagonists containing the conformationally constrained phenylalanine derivatives, including the new amino acid Xic

Synthesis of meta- and paracyclophanes containing unsaturated amino acid residues

4-Chlorobenzyl sulfonamide and sulfamide derivatives of histamine homologues: the design of potent histamine H3 receptor antagonists

An Efficient Synthesis of (2S) and (2R)-N-Benzoyl-2-t-butyl-4-methyleneoxazolidin-5-one

Histamine H 3 receptor antagonists

Application of 7-endo, 8-endo and 9-endo radical cyclisations to the synthesis of conformationally constrained amino acids and comparison with the corresponding Heck reactions

Synthesis and structural analysis of dehydrophenylalanine cyclophanes

2,7-Dioxo-2,3,4,5,6,7-hexahydro-1H-benzo[h][1,4]diazonine as a new template for the design of CCK(2) receptor antagonists

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