anti-Selective direct asymmetric Mannich reactions catalyzed by chiral pyrrolidine-based amino sulfonamides

Tetrahedron

Volumn 64, Issue 7, 2008, Pages 1197-1203

  Kano, Taichi ^a   Hato, Yoshio ^a   Yamamoto, Akihiro ^a   Maruoka, Keiji ^a  

^a KYOTO UNIVERSITY   (Japan)

Author keywords

Asymmetric synthesis; Enamine catalysis; Mannich reaction; Organocatalyst

Indexed keywords

1 BENZYL 3 (NONAFLUOROBUTYLSULFONAMIDO)PYRROLIDINE; 1 BENZYL 3 (TRIFLUOROMETHYLSULFONAMIDO)PYRROLIDINE; 1 BENZYL 3 AMINOPYRROLIDINE; 1 BENZYL 3,4 BIS(METHYLSULFOXY)PYRROLIDINE; 1 BENZYL 3,4 BIS(TRIFLUOROMETHYLSULFONAMIDO)PYRROLIDINE; 1 BENZYL 3,4 DIHYDROXYPYRROLIDINE 2,5 DIONE; 3 (NONAFLUOROBUTYLSULFONAMIDO)PYRROLIDINE; 3 (TRIFLUOROMETHYLSULFONAMIDO)PYRROLIDINE; 3,4 BIS(TRIFLUOROMETHYLSULFONAMIDO)PYRROLIDINE; 3,4 DIAMINO 1 BENZYLPYRROLIDINE; 3,4 DIAZIDO 1 BENZYLPYRROLIDINE; AMINO SULFONAMIDE DERIVATIVE; ETHYL 2 (4 METHOXYPHENYLAMINO) 2 (2' OXOCYCLOHEXYL)ACETATE; ETHYL 2 (4 METHOXYPHENYLAMINO) 2 (4' OXOTETRAHYDROPYRAN 3' YL)ACETATE; ETHYL 2 (4 METHOXYPHENYLAMINO) 2 (4' OXOTETRAHYDROTHIOPYRAN 3' YL)ACETATE; ETHYL 2 (4 METHOXYPHENYLAMINO) 3 METHYL 4 OXOHEXANOATE; ETHYL 2 (4 METHOXYPHENYLAMINO) 3 METHYL 4 OXOPENTANOATE; ETHYL 3 ETHYL 2 (4 METHOXYPHENYLAMINO) 4 METHYL 4 OXOHEPTANOATE; ETHYL 3 FORMYL 2 (4 METHOXYPHENYLAMINO) 4 METHYLPENTANOATE; ETHYL 3 FORMYL 2 (4 METHOXYPHENYLAMINO) 4,4 DEMETHYLPENTANOATE; ETHYL 3 FORMYL 2 (4 METHOXYPHENYLAMINO)BUTANOATE; ETHYL 3 FORMYL 2 (4 METHOXYPHENYLAMINO)PENTANOATE; PYRROLIDINE DERIVATIVE; SULFONAMIDE; UNCLASSIFIED DRUG;

ARTICLE; ASYMMETRIC CATALYSIS; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STRUCTURE; CHIRALITY; ENANTIOMER; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MANNICH REACTION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS;

EID: 37649001505     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2007.11.086     Document Type: Article

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