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Volumn 84, Issue 3, 2006, Pages 464-468

Chiral shift reagent catalyzed, diastereoselective imino Diels-Alder reaction - Synthesis of pyrazolyltetrahydroquinolines

(2) Sridhar, Radhakrishnan a Perumal, Paramasivan T a

a CENTRAL LEATHER RESEARCH INSTITUTE (India)

Author keywords

Antibacterial activity; Chiral shift reagent catalyst; Diastereoselectivity; Imino Diels Alder reaction; Pyrazolyltetrahydroquinolines

Indexed keywords

AGENTS; CATALYST ACTIVITY; REACTION KINETICS; SYNTHESIS (CHEMICAL);

ANTIBACTERIAL ACTIVITY; CHIRAL SHIFT REAGENT CATALYST; DIASTEREOSELECTIVITY; IMINO DIELS-ALDER REACTION; PYRAZOLYLTETRAHYDROQUINOLINES;

NITROGEN COMPOUNDS;

2 (1H INDOL 3 YL)TETRAHYDROQUINOLINE DERIVATIVE; ETHYL 4 (8 METHOXY 3A,4,5,9B TETRAHYDRO 3H CYCLOPENTA[C]QUINOLIN 4 YL) 1 (2,4 DINITROPHENYL) 1H PYRAZOLE 3 CARBOXYLATE; ETHYL 4 [(3AALPHA,4ALPHA,9BALPHA) 8 METHOXY 2,3,3A,4,5,9B HEXAHYDROFURO[3,2 C]QUINOLIN 4 YL] 1 (4 NITROPHENYL) 1H PYRAZOLE 3 CARBOXYLATE; ETHYL 4 [(3AALPHA,4BETA,9BALPHA) 8 CHLORO 2,3,3A,4,5,9B HEXAHYDROFURO[3,2 C]QUINOLIN 4 YL] 1 (2,4 DINITROPHENYL) 1H PYRAZOLE 3 CARBOXYLATE; IMINE; METHYL 4 (3A,4,5,9B TETRAHYDRO 3H CYCLOPENTA[C]QUINOLIN 4 YL) 1 (4 NITROPHENYL) 1H PYRAZOLE 3 CARBOXYLATE; METHYL 4 (8 METHOXY 3A,4,5,9B TETRAHYDRO 3H CYCLOPENTA[C]QUINOLIN 4 YL) 1 (4 NITROPHENYL) 1H PYRAZOLE 3 CARBOXYLATE; METHYL 4 [(4AALPHA,5BETA,10BALPHA) 9 METHOXY 3,4,4A,5,6,10B HEXAHYDRO 2H PYRANO[3,2 C]QUINOLIN 5 YL] 1 (4 NITROPHENYL) 1H PYRAZOLE 3 CARBOXYLATE; METHYL 4[(3AALPHA,4BETA,9BALPHA) 8 METHOXY 2,3,3A,4,5,9B HEXAHYDROFURO[3,2 C]QUINOLINE 4 YL] 1 (4 NITROPHENYL) 1H PYRAZOLE 3 CARBOXYLATE; PYRAZOLYLTETRAHYDROCYLOPENTAQUINOLINE DERIVATIVE; PYRAZOLYLTETRAHYDROQUINOLINE DERIVATIVE; PYRAZOYLTETRAHYDROPYRANOQUINOLINE DERIVATIVE; QUINOLINE DERIVATIVE; RIBAVIRIN; TETRAHYDROQUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

ANTIBACTERIAL ACTIVITY; ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; DIELS ALDER REACTION; DRUG STRUCTURE; DRUG SYNTHESIS; STEREOCHEMISTRY;

EID: 33745684110 PISSN: 00084042 EISSN: None Source Type: Journal
DOI: 10.1139/V06-017 Document Type: Article

Times cited : (3)

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