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Volumn , Issue 2, 2001, Pages 262-266
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An efficient synthesis of the potent dopamine D1 agonist dinapsoline by construction and selective reduction of 2′-azadimethoxybenzanthrone
a
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Author keywords
Acylation; Amide hydrolysis; Boron; Cyclization; Electrophilic aromatic substitution; Hydrogenation; Regioselective reduction; Suzuki cross coupling
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Indexed keywords
AMIDE;
BORONIC ACID DERIVATIVE;
CARBOXYLIC ACID DERIVATIVE;
CYANOBOROHYDRIDE SODIUM;
DINAPSOLINE;
DOPAMINE 1 RECEPTOR STIMULATING AGENT;
ISOQUINOLINE DERIVATIVE;
LITHIUM;
REDUCING AGENT;
SODIUM BOROHYDRIDE;
UNCLASSIFIED DRUG;
ACYLATION;
ARTICLE;
CYCLIZATION;
DRUG SYNTHESIS;
HYDROGENATION;
HYDROLYSIS;
PARKINSON DISEASE;
REACTION ANALYSIS;
REDUCTION;
STEREOCHEMISTRY;
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EID: 0035122628
PISSN: 00397881
EISSN: None
Source Type: Journal
DOI: 10.1055/s-2001-10809 Document Type: Article |
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Times cited : (8)
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References (21)
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