N-Tfa- and N-Fmoc-(α-aminoacyl)benzotriazoles as chiral C-acylating reagents under Friedel-Crafts reaction conditions

Journal of Organic Chemistry

Volumn 70, Issue 13, 2005, Pages 4993-5000

  Katritzky, Alan R ^a   Jiang, Rong ^a   Suzuki, Kazuyuki ^a  

^a University of Florida ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALUMINUM COMPOUNDS; AMINO ACIDS; BENZENE; KETONES; NITROGEN;

CHIRALITY; CYCLIZATION; INDOLES;

ORGANIC COMPOUNDS;

(ALPHA AMINOACYL)BENZOTRIAZOLE; 1 METHYLPYRROLE; 2,2,2 TRIFLUORO N [1 METHYL 2 (1 METHYL 1H INDOL 3 YL) 2 OXOETHYL]ACETAMIDE; 2,2,2 TRIFLUORO N [1 METHYL 2 (1 METHYL 1H PYRROL 2 YL) 2 OXOETHYL]ACETAMIDE; 2,2,2 TRIFLUORO N [1 METHYL 2 OXO 2 (H PYRROL 2 YL)ETHYL]ACETAMIDE; 2,2,2 TRIFLUORO N [1 OXO 2,3 DIHYDRO 1H INDEN 2 YL]ACETAMIDE; 2,2,2 TRIFLUORO N [2 (1H INDOL 3 YL) 1 METHYL 2 OXOETHYL]ACETAMIDE; 9H FLUOREN 9 YLMETHYL N [1 (1H INDOL 3 YL)CARBONYL] 3 (METHYLSULFANYL)PROPYL]CARBAMATE; 9H FLUOREN 9 YLMETHYL N [1 (1H INDOL 3 YLMETHYL) 2 OXO 2 (1 METHYL 1 H PYRROL 2 YL)ETHYL]CARBAMATE; 9H FLUOREN 9 YLMETHYL N [1 (1H INDOL 3 YLMETHYL) 2 OXO 2 (1 METHYL 1H INDOL 2 YL)ETHYL]CARBAMATE; 9H FLUOREN 9 YLMETHYL N [1 (1H INDOL 3YLCARBONYL) 3 (METHYLSULFANYL) PROPYL]CARBAMATE; 9H FLUOREN 9 YLMETHYL N [1 [(1 METHYL 1 H PYRROL 2 YL)CARBONYL] 3 (METHYLSULFANYL)PROPYL]CARBAMATE; 9H FLUOREN 9 YLMETHYL N [1 BENZYL 2 (1 METHYL 1H INDOL 3 YL) 2 OXOETHYL]CARBAMATE; 9H FLUOREN 9 YLMETHYL N [1 BENZYL 2 (1 METHYL 1H PYRROL 2 YL) 2 OXOETHYL]CARBAMATE; 9H FLUOREN 9 YLMETHYL N [1 BENZYL 2 BENZOTRIAZOL 1 YL 2 OXOETHYL] CARBAMATE; 9H FLUOREN 9 YLMETHYL N [1 BENZYL 2 OXO 2 (1H INDOL 3 YL)ETHYL]CARBAMATE; 9H FLUOREN 9 YLMETHYL N [1 BENZYL 2 OXO 2 (1H PYRROL 2 YL)ETHYL]CARBAMATE; 9H FLUOREN 9 YLMETHYL N [1H INDOL 3 YLMETHYL) 2 OXO 2 (1H PYRROL 2 YL)ETHYL]CARBAMATE; 9H FLUOREN 9 YLMETHYL N [2 (1H 1,2,3 BENZOTRIAZOL 1 YL) 1 METHYL 2 OXOETHYL]CARBAMATE; 9H FLUOREN 9 YLMETHYL N [2 (1H INDOL 3 YL) 1 (1H INDOL 3 YLMETHYL) 2 OXOETHYL]CARBAMATE; 9H FLUOREN 9 YLMETHYL N [3 (METHYLSUFANYL) 1 (1H PYRROL 2 YLCARBONYL)PROPYL]CARBAMATE; 9H FLUOREN 9 YLMETHYL N [3 OXO 1,2,3,4 TETRAHYDROCYCLOPENTA[B]INDOL 2 YL]CARBAMATE; 9H FLUOREN 9 YLMETHYL N [4 BENZOTRIAZOL 1 YL 1 (BENZOTRIAZOL 1 YL CARBONYL) 4 OXOBUTYL]CARBAMATE; 9H FLUOREN P YLMETHYL N [4 OXO 4 (1H PYRROL 2 YL) 1 (1H PYRROL 2 YLCARBONYL)BUTYL]CARBAMATE; 9H FLUOREN YLMETHYL N [1 METHYL 2 (1 METHYL 1H INDOL 3 YL) 2 OXO ETHYL]CARBAMATE; BENZENE; BENZOTRIAZOLE DERIVATIVE; DIKETONE; HETEROCYCLIC KETONE; INDOLE; N [1 BENZYL 2 (1 METHYL 1H INDOL 3 YL) 2 OXOETHYL] 2,2,2 TRIFLUOROACETAMIDE; N [1 BENZYL 2 (1 METHYL 1H PYRROL 2 YL) 2 OXOETHYL] 2,2,2 TRIFLUOROACETAMIDE; N [1 BENZYL 2 (1H INDOL 3 YL) 2 OXOETHYL] 2,2,2 TRIFLUOROACETAMIDE; N [1 BENZYL 2 OXO 2 (1H PYRROL 3 YL)ETHYL] 2,2,2 TRIFLUOROACETAMIDE; N [1 BENZYL 2 OXO 2 PHENYLETHYL] 2,2,2 TRIFLUOROACETAMIDE; N [2 (1H 1,2,3 BENZOTRIAZOL 1 YL) 1 BENZYL 2 OXOETHYL] 2,2,2 TRIFLUOROACETAMIDE; N [2 (1H 1,2,3 BENZOTRIAZOL 1 YL) 1 BENZYL 2 OXOETHYL]2,2,2 TRIFLUOROACETAMIDE; N [2 (1H 1,2,3 BENZOTRIAZOL 1 YL) 1 METHYL 2 OXOETHYL] 2,2,2 TRIFLUOROACETAMIDE; PYRROLE; UNCLASSIFIED DRUG;

ACYLATION; ARTICLE; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHIRALITY; CYCLIZATION; ENANTIOMER; FRIEDEL CRAFTS REACTION; NUCLEAR MAGNETIC RESONANCE;

EID: 20844453422     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo050226q     Document Type: Article

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