SCOPUS 정보 검색 플랫폼

Volumn 8, Issue 9, 2010, Pages 2252-2259

Highly efficient synthesis and characterization of the GPR30-selective agonist G-1 and related tetrahydroquinoline analogs

(9) Burai, Ritwik a Ramesh, Chinnasamy a Shorty, Marvin a Curpan, Ramona b,c Bologa, Cristian c Sklar, Larry A c,d Oprea, Tudor c,d Prossnitz, Eric R c,d Arterburn, Jeffrey B a,d

a NEW MEXICO STATE UNIVERSITY (United States)

b ACADEMY OF ROMANIAN SCIENTISTS (Romania)

c UNIVERSITY OF NEW MEXICO HEALTH SCIENCES CENTER (United States)

d UNIVERSITY OF NEW MEXICO (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DIASTEREO-SELECTIVITY; DIELS-ALDER CYCLIZATION; EFFICIENT SYNTHESIS; MULTICOMPONENTS; REACTION TEMPERATURE; TETRAHYDROQUINOLINE;

CYCLIZATION; SCANDIUM; SCANDIUM COMPOUNDS;

SYNTHESIS (CHEMICAL);

1 (4 (6 BROMOBENZO(1,3)DIOXOL 5 YL) 3A,4,5,9B TETRAHYDRO 3H CYCLOPENTA(C)QUINOLIN 8 YL)ETHANONE; 1,2,3,4 TETRAHYDROQUINOLINE; 1,2,3,4-TETRAHYDROQUINOLINE; 1-(4-(6-BROMOBENZO(1,3)DIOXOL-5-YL)-3A,4,5,9B-TETRAHYDRO-3H-CYCLOPENTA(C)QUINOLIN-8-YL)ETHANONE; CYCLOPENTANE DERIVATIVE; G PROTEIN COUPLED RECEPTOR; QUINOLINE DERIVATIVE;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; DRUG POTENTIATION; STEREOISOMERISM; STRUCTURE ACTIVITY RELATION; SYNTHESIS;

CYCLOPENTANES; MOLECULAR STRUCTURE; QUINOLINES; RECEPTORS, G-PROTEIN-COUPLED; STEREOISOMERISM; STRUCTURE-ACTIVITY RELATIONSHIP;

ALNUS;

EID: 77951119518 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/c001307b Document Type: Article

Times cited : (44)

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