Enantioselective synthesis of highly substituted chromans by a zinc(ii)-catalyzed tandem friedel-crafts alkylation/michael addition reaction

Synthesis (Germany)

Volumn 45, Issue 5, 2013, Pages 601-608

  Li, Chao ^a   Liu, Feng Lei ^a   Zou, You Quan ^a   Lu, Liang Qiu ^a   Chen, Jia Rong ^a   Xiao, Wen Jing ^a  

^a China Normal University   (China)

Author keywords

1 methylindole; chroman; Friedel Crafts alkylation; nitroolefin enoate; tandem reaction

Indexed keywords

1-METHYLINDOLE; CHROMAN; FRIEDEL-CRAFTS ALKYLATION; NITROOLEFIN ENOATE; TANDEM REACTION;

ADDITION REACTIONS; CATALYSIS; ENANTIOSELECTIVITY;

ZINC COMPOUNDS;

4 CHROMANONE DERIVATIVE; CROMAKALIN; ETHYL 2 [4 (5 BROMO 1 METHYL 1H INDOL 3 YL) 3 NITROCHROMAN 2 YL]ACETATE; ETHYL 2 [4 (5 FLUORO 1 METHYL 1H INDOL 3 YL) 3 NITROCHROMAN 2 YL]ACETATE; ETHYL 2 [6 BROMO 4 (1 METHYL 1H INDOL 3 YL) 3 NITROCHROMAN 2 YL]ACETATE; ETHYL 2 [6 CHLORO 4 (1 METHYL 1H INDOL 3 YL) 3 NITROCHROMAN 2 YL]ACETATE; ETHYL 2 [6 FLUORO 4 (1 METHYL 1H INDOL 3 YL) 3 NITROCHROMAN 2 YL]ACETATE; ETHYL 2 [6 METHOXY 4 (1 METHYL 1H INDOL 3 YL) 3 NITROCHROMAN 2 YL]ACETATE; ETHYL 2 [6 METHYL 4 (1 METHYL 1H INDOL 3 YL) 3 NITROCHROMAN 2 YL]ACETATE; ETHYL 2 [7 METHOXY 4 (1 METHYL 1H INDOL 3 YL) 3 NITROCHROMAN 2 YL]ACETATE; ETHYL 2-[4-(1,2-DIMETHYL 1H INDOL 3 YL) 3 NITROCHROMAN 2 YL]ACETATE; ETHYL 2-[4-(1,5-DIMETHYL 1H INDOL 3 YL) 3 NITROCHROMAN 2 YL]ACETATE; ETHYL 2-[4-(1,6-DIMETHYL 1H INDOL 3 YL) 3 NITROCHROMAN 2 YL]ACETATE; ETHYL 2-[4-(1,7-DIMETHYL 1H INDOL 3 YL) 3 NITROCHROMAN 2 YL]ACETATE; SICCANIN; UNCLASSIFIED DRUG; VISNADINE; ZINC;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYSIS; CHEMICAL REACTION; CHIRALITY; CYCLIZATION; DRUG STRUCTURE; ENANTIOSELECTIVITY; FRIEDEL CRAFTS REACTION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MICHAEL ADDITION; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY;

EID: 84874281025     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0032-1318200     Document Type: Article

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