Catalytic and asymmetric Friedel-Crafts alkylation of indoles with nitroacrylates. Application to the synthesis of tryptophan analogues

Tetrahedron

Volumn 63, Issue 24, 2007, Pages 5173-5183

  Sui, Yong ^a,b   Liu, Li ^a   Zhao, Jun Ling ^a,b   Wang, Dong ^a   Chen, Yong Jun ^a  

^a INSTITUTE OF CHEMISTRY   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

Author keywords

Catalytic and asymmetric Friedel Crafts alkylation; Chiral DiPhBOX Cu(II) complex; Indole; Nitroacrylate; Tryptophan

Indexed keywords

ACRYLIC ACID; ETHYL 2 ACETAMIDO 3 (1H INDOL 3 YL) 3 4 TOLYLPROPANOIC ACID; ETHYL 3 (1H INDOL 3 YL) 2 NITRO 3 4 TOLYLPROPANOIC ACID; ETHYL 3 (1H INDOL 3 YL) 3 (4 METHOXYPHENYL) 2 NITROPROPANOIC ACID; ETHYL 3 (2 METHYL 1H INDOL 3 YL) 2 NITRO 3 4 TOLYLPROPANOIC ACID; ETHYL 3 (4 BROMO 1H INDOL 3 YL) 3 (4 CHLOROPHENYL) 2 NITROPROPANOIC ACID; ETHYL 3 (4 CHLOROPHENYL) 3 (1H INDOL 3 YL) 2 NITROPROPANOIC ACID; ETHYL 3 (5 BROMO 1H INDOL 3 YL) 2 NITRO 3 4 TOLYLPROPANOIC ACID; ETHYL 3 (5 BROMO 1H INDOL 3 YL) 3 (4 CHLOROPHENYL) 2 (PHENYLSULFONAMIDO)PROPANOIC ACID; ETHYL 3 (5 BROMO 1H INDOL 3 YL) 3 (4 CHLOROPHENYL) 2 NITROPROPANOIC ACID; ETHYL 3 (5 BROMO 1H INDOL 3 YL) 3 (4 METHOXYPHENYL) 2 NITROPROPANOIC ACID; ETHYL 3 (5 METHOXY 1H INDOL 3 YL) 2 NITRO 3 4 TOLYLPROPANOIC ACID; ETHYL 3 (5 METHOXY 1H INDOL 3 YL) 3 (4 METHOXYPHENYL) 2 NITROPROPANOIC ACID; ETHYL 3 (BENZO[D][1,3]DIOXOL 5 YL) 3 (1H INDOL 3 YL) 2 NITROPROPANOIC ACID; ETHYL 3 [5 (BENZYLOXY) 1H INDOL 3 YL] 2 NITRO 3 4 TOLYLPROPANOIC ACID; INDOLE DERIVATIVE; METHYL 3 (3 ETHOXY 2 NITRO 3 OXO 1 4 TOLYLPROPYL) 1H INDOLE 5 CARBOXYLIC ACID; METHYL 3 [3 ETHOXY 1 (4 METHOXYPHENYL) 2 NITRO 3 OXOPROPYL] 1H INDOLE 5 CARBOXYLIC ACID; NITROACRYLIC ACID; TERT BUTYL 3 (4 CHLOROPHENYL) 3 (1H INDOL 3 YL) 2 NITROPROPANOIC ACID; TRYPTOPHAN DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHIRALITY; CRYSTAL STRUCTURE; ENANTIOSELECTIVITY; FRIEDEL CRAFTS REACTION; PRIORITY JOURNAL; STEREOCHEMISTRY; SYNTHESIS;

EID: 34247847623     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2007.03.175     Document Type: Article

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