Asymmetric domino aza-Michael-Michael reaction of o-N-protected aminophenyl α,β-unsaturated ketones: Construction of chiral functionalized tetrahydroquinolines

Tetrahedron

Volumn 70, Issue 34, 2014, Pages 5114-5121

  Kim, Shinae ^a   Kang, Ki Tae ^a   Kim, Sung Gon ^a  

^a Kyonggi University   (South Korea)

Author keywords

Asymmetric catalysis; Domino reaction; Michael addition; Organocatalysis; Tetrahydroquinoline

Indexed keywords

1 (2 CHLOROPHENYL) 2 ( 1,2,3,4 TETRAHYDRO 3 NITRO 2 PHENYL 1 TOSYLQUINOLIN 4 YL)ETHANONE; 1 (3 CHLOROPHENYL) 2 ( 1,2,3,4 TETRAHYDRO 3 NITRO 2 PHENYL 1 TOSYLQUINOLIN 4 YL)ETHANONE; 1 (4 CHLOROPHENYL) 2 ( 1,2,3,4 TETRAHYDRO 3 NITRO 2 PHENYL 1 TOSYLQUINOLIN 4 YL)ETHANONE; 2 ( 1,2,3,4 TETRAHYDRO 3 NITRO 2 PHENYL 1 TOSYLQUINOLIN 4 YL) 1 P TOLYLETHANONE; 2 ( 6 BROMO 1,2,3,4 TETRAHYDRO 3 NITRO 2 PHENYL 1 TOSYLQUINOLIN 4 YL) 1 PHENYLETHANONE; 2 ( 6 CHLORO 1,2,3,4 TETRAHYDRO 3 NITRO 2 PHENYL 1 TOSYLQUINOLIN 4 YL) 1 PHENYLETHANONE; 2 ( 7 CHLORO 1,2,3,4 TETRAHYDRO 3 NITRO 2 PHENYL 1 TOSYLQUINOLIN 4 YL) 1 PHENYLETHANONE; 2 (1,2,3,4 TETRAHYDRO 2 (2 METHOXYPHENYL) 3 NITRO 1 TOSYLQUINOLIN 4 YL) 1 PHENYLETHANONE; 2 (1,2,3,4 TETRAHYDRO 2 (3 METHOXYPHENYL) 3 NITRO 1 TOSYLQUINOLIN 4 YL) 1 PHENYLETHANONE; 2 (1,2,3,4 TETRAHYDRO 2 (3,4 DIMETHOXYPHENYL) 3 NITRO 1 TOSYLQUINOLIN 4 YL) 1 PHENYLETHANONE; 2 (1,2,3,4 TETRAHYDRO 2 (4 METHOXYPHENYL) 3 NITRO 1 TOSYLQUINOLIN 4 YL) 1 PHENYLETHANONE; 2 (1,2,3,4 TETRAHYDRO 2 ISOPROPYL 3 NITRO 1 TOSYLQUINOLIN 4 YL) 1 PHENYLETHANONE; 2 (1,2,3,4 TETRAHYDRO 3 NITRO 2 (4 NITROPHENYL) 1 TOSYLQUINOLIN 4 YL) 1 PHENYLETHANONE; 2 (1,2,3,4 TETRAHYDRO 3 NITRO 2 (THIOPHEN 2 YL) 1 TOSYLQUINOLIN 4 YL) 1 PHENYLETHANONE; 2 (1,2,3,4 TETRAHYDRO 3 NITRO 2 P TOLYL 1 TOSYLQUINOLIN 4 YL) 1 PHENYLETHANONE; 2 (1,2,3,4 TETRAHYDRO 3 NITRO 2 PHENYL 1 TOSYLQUINOLIN 4 YL) 1 (4 METHOXYPHENYL)ETHANONE; 2 (1,2,3,4 TETRAHYDRO 3 NITRO 2 PHENYL 1 TOSYLQUINOLIN 4 YL) 1 PHENYLETHANONE; 2 (1,2,3,4 TETRAHYDRO 6 METHYL 3 NITRO 2 PHENYL 1 TOSYLQUINOLIN 4 YL) 1 PHENYLETHANONE; 2 (1,2,3,4 TETRAHYDRO 8 METHYL 3 NITRO 2 PHENYL 1 TOSYLQUINOLIN 4 YL) 1 PHENYLETHANONE; 2 (2 (2 BROMOPHENYL) 1,2,3,4 TETRAHYDRO 3 NITRO 1 TOSYLQUINOLIN 4 YL) 1 PHENYLETHANONE; 2 (2 (2 CHLOROPHENYL) 1,2,3,4 TETRAHYDRO 3 NITRO 1 TOSYLQUINOLIN 4 YL) 1 PHENYLETHANONE; 2 (2 (4 CHLOROPHENYL) 1,2,3,4 TETRAHYDRO 3 NITRO 1 TOSYLQUINOLIN 4 YL) 1 PHENYLETHANONE; 2 (2 (BENZO[D][1,3]DIOXOL 5 YL) 1,2,3,4 TETRAHYDRO 3 NITRO 1 TOSYLQUINOLIN 4 YL) 1 PHENYLETHANONE; 2 (2 (FURAN 2 YL) 1,2,3,4 TETRAHYDRO 3 NITRO 1 TOSYLQUINOLIN 4 YL) 1 PHENYLETHANONE; CARBENE; CARBONYL DERIVATIVE; KETONE DERIVATIVE; QUINOLINE DERIVATIVE; TETRAHYDROQUINOLINE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG; ALKENE; QUINOLONE DERIVATIVE;

ARTICLE; CHIRALITY; CONJUGATE; CYCLIZATION; DRUG SYNTHESIS; ENANTIOSELECTIVITY; METHODOLOGY; MICHAEL ADDITION; PRIORITY JOURNAL; ASYMMETRIC CATALYSIS; CATALYST; DIASTEREOISOMER; HYDROGEN BOND; REACTION TIME; STEREOCHEMISTRY; STEREOSPECIFICITY;

EID: 84903373572     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2014.05.114     Document Type: Article

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