Switching of enantioselectivity in the catalytic addition of diethylzinc to aldehydes by regioisomeric chiral 1,3-amino sulfonamide ligands

Journal of Organic Chemistry

Volumn 76, Issue 13, 2011, Pages 5413-5428

  Hirose, Takuji ^a   Sugawara, Kazuyuki ^a   Kodama, Koichi ^a  

^a SAITAMA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ALIPHATIC ALDEHYDES; AS-LIGANDS; CATALYTIC ADDITION; DIETHYLZINC; ENANTIOSELECTIVE ADDITION; REACTION CONDITIONS; REGIOISOMERS; SEC-ALCOHOLS; SECONDARY ALCOHOLS; STRUCTURAL SURVEYS;

ALDEHYDES; AMIDES; CHIRALITY; ENANTIOMERS; ENANTIOSELECTIVITY; ORGANIC COMPOUNDS; STEREOCHEMISTRY; STRUCTURAL OPTIMIZATION; SULFUR COMPOUNDS;

LIGANDS;

2 BENZAMIDOCYCLOHEXANECARBOXYLIC ACID; 4 METHYL N [[2 (METHYLAMINO)CYCLOHEXYL]METHYL]BENZENESULFONAMIDE; 4 METHYL N [[2 (PIPERIDIN 1 YL)CYCLOHEXYL]METHYL]BENZENESULFONAMIDE; 4 METHYL N [[2 (PYRROLIDIN 1 YL)CYCLOHEXYL]METHYL]BENZENESULFONAMIDE; 4 METHYL N[2 [(METHYLAMINO)METHYL]CYCLOHEXYL]BENZENESULFONAMIDE; ALCOHOL DERIVATIVE; ALDEHYDE; BENZENESULFONAMIDE DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; DIETHYLZINC; LIGAND; N [2 [(DIMETHYLAMINO)METHYL]CYCLOHEXYL] 4 METHYLBENZENESULFONAMIDE; N [2 AMINOMETHYL)CYCLOHEXYL] 4 METHYLBENZENESULFONAMIDE; N [[2 (BENZYLAMINO)CYCLOHEXYL]METHYL] 4 METHYLBENZENESULFONAMIDE; N [[2 (DIETHYLAMINO)CYCLOHEXYL]METHYL] 4 METHYLBENZENESULFONAMIDE; N [[2 (DIMETHYLAMINO)CYCLOHEXYL]METHYL] 4 METHYLBENZENESULFONAMIDE; N [[2 (DIPROPYLAMINO)CYCLOHEXYL]METHYL] 4 METHYLBENZENESULFONAMIDE; N [[2 AMINOCYCLOHEXYL]METHYL] 4 METHYLBENZENESULFONAMIDE; SULFONAMIDE; TERTIARY AMINE; TOLUENESULFONAMIDE DERIVATIVE; UNCLASSIFIED DRUG;

ADDITION REACTION; ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHIRALITY; ENANTIOMER; ENANTIOSELECTIVITY; QUANTITATIVE ANALYSIS; REACTION ANALYSIS; REACTION OPTIMIZATION; STEREOCHEMISTRY; STEREOISOMERISM;

ALDEHYDES; CATALYSIS; LIGANDS; MOLECULAR STRUCTURE; ORGANOMETALLIC COMPOUNDS; STEREOISOMERISM; SULFONAMIDES;

EID: 79959669557     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo200834n     Document Type: Article

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