Angela R. Williams

发表

Comparison of the functional blockade of rat substance P (NK1) receptors by GR205171, RP67580, SR140333 and NKP-608

G. Bentley, K. Tsao, R. Kilburn, 2003, Neuropharmacology.

Effects of the bradykinin B1 receptor antagonist des-Arg9[Leu8]bradykinin and genetic disruption of the B2 receptor on nociception in rats and mice

S. Boyce, J. Hess, R. Hill, 1997, Pain.

A New Series of Proton/Charge Transfer Molecules: Synthesis and Spectral Studies of 2‐(5‐Aryl‐1‐carbomethoxy‐1H‐pyrazol‐3‐yl)phenols

D. Hurst, Carrie E. Halkyard, Mary E. Rampey, 1999 .

The preparation of 4,5-dihydro-2H-benz[e]indazoles from dilithiated 2-tetralone phenylhydrazone and aromatic esters

D. Hurst, F. Heldrich, C. F. Beam, 1999 .

The Preparation Of 2-[4,5-Dihydro-3-Aryl-5-Isoxazolyl]-Phenols From C(α),O-Dilithiooximes and Lithiated Hydroxyaryl Aldehydes

D. Hurst, C. F. Beam, Angela R. Williams, 1999 .

The Preparation of 2-(4-Oxo-4H-1-benzopyran-2-yl)-1-phenyl-ethanones by the Condensation/Cyclization of Dilithiated 1-Benzoylacetone with Lithiated Methyl Salicylates

D. Hurst, C. F. Beam, Angela R. Williams, 1998 .

Spirocyclic NK(1) antagonists II: [4.5]-spiroethers.

C. Swain, B. Williams, G. Chicchi, 2002, Bioorganic & medicinal chemistry letters.

Preparation of N-aryl-4-oxo-4H-1-benzothiopyran-2-acetamides from trilithiated acetoacetanilides and lithiated methyl thiosalicylate

D. Hurst, Mary E. Rampey, Shannon L. Studer-Martinez, 1999 .

A new preparation of substituted 4H‐1‐benzothiopyran‐4‐ones from c(α)N‐benzoylhydrazones or c(α)N‐carboalkoxyhydrazones and methyl thiosalicylate

D. Hurst, C. F. Beam, Angela R. Williams, 1998 .

The Preparation of 4-Oxo-N-aryl-4H-1-benzopyran-2-acetamides by the Condensation/Cyclization of Trilithiated Acetoacetanilides with Lithiated Methyl Salicylates.

D. Hurst, K. W. Chan, Shannon Studer Martinez, 1999 .

The preparation of 4-oxo-N-aryl-4H-1-benzopyran-2-acetamides by the condensation/cyclization of trilithiated acetoacetanilides with lithiated methyl salicylates

D. Hurst, K. W. Chan, Shannon Studer Martinez, 1998 .

Preparation of N-Aryl-4-oxo-4H-1-benzothiopyran-2-acetamides from Trilithiated Acetoacetanilides and Lithiated Methyl Thiosalicylate.

D. Hurst, Mary E. Rampey, Shannon L. Studer-Martinez, 2010 .

A New Preparation of Substituted 4H‐1‐Benzothiopyran‐4‐ones from C(α),N‐Benzoylhydrazones or C(α),N‐Carboalkoxyhydrazones and Methyl Thiosalicylate.

D. Hurst, C. F. Beam, Angela R. Williams, 1998 .

Preparation of Benz[b]Indeno[1,2-e]Pyran-11(6H)-Ones and Benz[b]Indeno[1,2-e]Thiopyran-11(6H)-One from Dilithiated 2-Indanone and Lithiated Methyl Salicylates or Lithiated Methyl Thiosalicylate

C. F. Beam, Angela R. Williams, Jessica D. Townsend, 2000 .

Structural optimization affording 2-(R)-(1-(R)-3, 5-bis(trifluoromethyl)phenylethoxy)-3-(S)-(4-fluoro)phenyl-4- (3-oxo-1,2,4-triazol-5-yl)methylmorpholine, a potent, orally active, long-acting morpholine acetal human NK-1 receptor antagonist.

J. Metzger, M. Maccoss, D. Macintyre, 1998, Journal of medicinal chemistry.

Phosphorylated morpholine acetal human neurokinin-1 receptor antagonists as water-soluble prodrugs.

J. Metzger, M. Maccoss, D. Macintyre, 2000, Journal of medicinal chemistry.