A practical synthesis of a potent δ-opioid antagonist: Use of a modified Knorr pyrrole synthesis

Organic Process Research and Development

Volumn 8, Issue 2, 2004, Pages 279-282

  Bellingham, Richard K ^a   Carey, John S ^a   Hussain, Nigel ^a   Morgan, David O ^a   Oxley, Paul ^a   Powling, Laurence C ^a  

^a GLAXOSMITHKLINE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

1 CHLOROETHYLCARBAMATE; 5,6,6A,7,10,11 HEXAHYDRO 6A HYDROXY 8 METHYL N (1 METHYLETHYL) N (PHENYLETHYL) 6,11A (IMINOETHANO) 11AH NAPHTH[2,1 F]INDOLE 9 CARBOXAMIDE; AMINOKETONE; CARBAMIC ACID DERIVATIVE; DELTA OPIATE RECEPTOR ANTAGONIST; OXIME; PHENYLHYDRAZONE DERIVATIVE; SB 342219; TRICHLOROETHYLCARBAMATE; UNCLASSIFIED DRUG; ZINC;

ARTICLE; CHEMICAL REACTION; DEMETHYLATION; DRUG ISOLATION; DRUG STRUCTURE; DRUG SYNTHESIS; HYDROGENATION; HYDROLYSIS; KNORR PYRROLE REACTION; REACTION ANALYSIS; REDUCTION; STRUCTURE ANALYSIS;

EID: 1842506620     PISSN: 10836160     EISSN: None     Source Type: Journal    
DOI: 10.1021/op034198u     Document Type: Article

References (7)

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