SnCl 2-catalyzed selective atom economic imino Diels-Alder reaction: Synthesis of 2-(1 H-pyrrolo[2,3-b ]pyridin-3-yl)quinolines

Journal of Organic Chemistry

Volumn 77, Issue 3, 2012, Pages 1468-1476

  Suresh, Rajendran ^a,b   Muthusubramanian, Shanmugam ^a   Senthilkumaran, Rajendran ^b   Manickam, Govindaswamy ^b  

^a MADURAI KAMARAJ UNIVERSITY   (India)

^b SYNGENE INTERNATIONAL LTD   (India)

Author keywords

[No Author keywords available]

Indexed keywords

DIELS-ALDER REACTION; MULTI-COMPONENT REACTIONS; QUINOLINE DERIVATIVE;

CHEMISTRY; ORGANIC COMPOUNDS;

CATALYSIS;

2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3 B]PYRIDIN 3 YL) 4 (THIOPHEN 3 YL)BENZO[H]QUINOLINE; 2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3 B]PYRIDIN 3 YL) 4 (THIOPHEN 3YL) 7 (TRIFLUOROMETHYL)QUINOLINE; 2 (1 (PHENYLSULFONYL)1H PYRROLO[2,3 B]PYRIDIN 3 YL) 4 (THIOPHEN 3 YL) 5 (TRIFLUOROMETHYL)QUINOLINE; 3 (6 METHYL 2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3 B]PYRIDIN 3 YL)QUINOLIN 4 YL)PHENOL; 3 (8 BROMO 2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3-B]PYRIDIN 3 YL)QUINOLIN 4 YL)PHENOL; 4 (2 METHOXYPHENYL) 2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3 B]PYRIDIN 3 YL)QUINOLINE 8 CARBONITRILE; 4 (2 METHOXYPHENYL) 5 NITRO 2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3 B]PYRIDIN 3 YL)QUINOLINE; 4 (2 METHOXYPHENYL) 6 NITRO 2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3 B]PYRIDIN 3 YL)QUINOLINE; 4 (2 METHOXYPHENYL) 7 NITRO 2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3 B]PYRIDIN 3 YL)QUINOLINE; 4 (4 ETHYLPHENYL) 2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3 B]PYRIDIN 3 YL) 6 (TRIFLUOROMETHYL)QUINOLINE; 4 (4 ETHYLPHENYL) 2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3 B]PYRIDIN 3 YL) 8 (TRIFLUOROMETHYL)QUINOLINE; 4 (BIPHENYL 4 YL) 2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3 B]PYRIDIN 3 YL) 6 (TRIFLUOROMETHYL)QUINOLINE; 4 (BIPHENYL 4 YL) 2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3 B]PYRIDIN 3 YL)QUINOLINE 5 CARBONITRILE; 4 (BIPHENYL 4 YL) 2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3 B]PYRIDIN 3 YL)QUINOLINE 7 CARBONITRILE; 4 CYCLOHEXENYL 6 METHOXY 2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3 B]PYRIDIN 3 YL)QUINOLINE; 4 CYCLOHEXENYL 8 METHOXY 2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3 B]PYRIDIN 3 YL)QUINOLINE; 4 PHENYL 2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3 B]PYRIDIN 3 YL)QUINOLINE; 4 PHENYL 2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3 B]PYRIDIN 3 YL)QUINOLINE 6 CARBONITRILE; 5 METHOXY 4 PHENYL 2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3 B]PYRIDIN 3 YL)QUINOLINE; 6 BROMO 2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3 B]PYRIDIN 3 YL) 4 (THIOPHEN 3 YL)QUINOLINE; 6 METHOXY 4 (2 METHOXYPHENYL) 2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3B]PYRIDIN 3 YL)QUINOLINE; 6 METHOXY 4 PHENYL 2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3 B]PYRIDIN 3 YL)QUINOLINE; 6 NITRO 4 PHENYL 2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3 B]PYRIDIN 3 YL)QUINOLINE; 7 METHOXY 4 PHENYL 2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3 B]PYRIDIN 3 YL)QUINOLINE; 8 CHLORO 4 CYCLOHEXENYL 2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3 B]PYRIDIN 3 YL)QUINOLINE; 8 NITRO 2 (1 (PHENYLSULFONYL) 1H PYRROLO[2,3 B]PYRIDIN 3 YL) 4 (THIOPHEN 3 YL)QUINOLINE; IMINO ACID; QUINOLINE DERIVATIVE; TIN CHLORIDE; UNCLASSIFIED DRUG; UNINDEXED DRUG; IMINE; STANNOUS CHLORIDE; TIN DERIVATIVE;

ARTICLE; ATOM; CATALYSIS; CYCLOADDITION; DIELS ALDER REACTION; ONE POT SYNTHESIS; STEREOCHEMISTRY; STOICHIOMETRY; CHEMISTRY; METHODOLOGY; SYNTHESIS;

CATALYSIS; CHEMISTRY TECHNIQUES, SYNTHETIC; IMINES; QUINOLINES; TIN COMPOUNDS;

EID: 84856683100     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo202256z     Document Type: Article

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