15 articles for WC Randall
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Synthesis of 4-substituted 2H-naphth[1,2-b]-1,4-oxazines, a new class of dopamine agonists.

TBA
Synthesis of (7R)-7H-indolo[3,4-gh][1,4]benzoxazines, a new class of D-heteroergolines with dopamine agonist activity.

TBA
Inhibitors of glycolic acid oxidase. 4-substituted 2,4-dioxobutanoic acid derivatives.

TBA
Inhibitors of gastric acid secretion: 3,4-diamino-1,2,5-thiadiazole 1-oxides and 1,1-dioxides as urea equivalents in a series of histamine H2-receptor antagonists.

TBA
4-substituted thiophene- and furan-2-sulfonamides as topical carbonic anhydrase inhibitors.

Merck Research Laboratories
Thienothiopyran-2-sulfonamides: novel topically active carbonic anhydrase inhibitors for the treatment of glaucoma.

Merck Sharp and Dohme
Thienothiopyran-2-sulfonamides: a novel class of water-soluble carbonic anhydrase inhibitors.

TBA
Synthesis and receptor binding studies relevant to the neuroleptic activities of some 1-methyl-4-piperidylidene-9-substituted-pyrrolo[2,1-b][3]benzazepine derivatives.

TBA
alpha-Adrenergic activities of some substituted 2-(aminomethyl)imidazolines.

TBA
Sulfonylmethanesulfonamide inhibitors of carbonic anhydrase.

Merck Research Laboratories
Pyridinylpiperazines, a new class of selective alpha 2-adrenoceptor antagonists.

TBA
Adrenoceptor and tetrabenazine antagonism activities of some pyridinyltetrahydropyridines.

TBA
N-(1,3,4,6,7,12b-hexahydro-2H-benzo[b]furo[2,3-a]quinolizin -2-yl)-N- methyl-2-hydroxyethane-sulfonamide: a potent and selective alpha 2-adrenoceptor antagonist.

TBA
Structure-affinity relationships of arylquinolizines at alpha-adrenoceptors.

Merck Sharp & Dohme Research Laboratories
Thieno[2,3-b]furan-2-sulfonamides as topical carbonic anhydrase inhibitors.

Merck Research Laboratories