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Volumn , Issue 17, 2003, Pages 3300-3307

Synthesis of 1-(m-hydroxybenzyl)-substituted 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid derivatives as opioid peptide mimetics - Unexpected amide bond cleavages under mild conditions

(4) Mannekens, Els a Crisma, Marco b Van Cauwenberghe, Sylvia a Tourwé, Dirk a

a VRIJE UNIVERSITEIT BRUSSEL (Belgium)

b CNR (Italy)

Author keywords

Alkylations; Asymmetric synthesis; Peptidomimetics; Receptors; Tetrahydroisoquinolines

Indexed keywords

1 (3 HYDROXYBENZYL) 1,2,3,4 TETRAHYDROISOQUINOLINE 3 CARBOXYLIC ACID DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; DELTA OPIATE RECEPTOR; DIPEPTIDE DERIVATIVE; GLYCINE 1 (3 HYDROXYBENZYL) 1,2,3,4 TETRAHYDROISOQUINOLINE 3 CARBOXYLIC ACID PHENYLALANINE HYDROXIDE; LIGAND; MORPHINE; N GLYCYL 1 (3 HYDROXYBENZYL) 1,2,3,4 TETRAHYDROISOQUINOLINE 3 CARBOXYLIC ACID; OPIATE PEPTIDE; UNCLASSIFIED DRUG;

ADDITION REACTION; ALKYLATION; ANALGESIC ACTIVITY; ANIMAL EXPERIMENT; ARTICLE; CHEMICAL BOND; CHEMICAL REACTION; CONTROLLED STUDY; DEPROTECTION REACTION; DISSOCIATION; DRUG EFFECT; DRUG RECEPTOR BINDING; DRUG STRUCTURE; DRUG SYNTHESIS; HUMAN; HUMAN CELL; NONHUMAN; PHARMACOPHORE; RAT; REACTION ANALYSIS; RECEPTOR AFFINITY; RECEPTOR BLOCKING; STEREOCHEMISTRY; SUBSTITUTION REACTION;

EID: 0043287137 PISSN: 1434193X EISSN: None Source Type: Journal
DOI: 10.1002/ejoc.200300175 Document Type: Article

Times cited : (12)

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