Indium(III) bromide catalyzed rapid propargylation of heteroaromatic systems by α-aryl-substituted propargyl alcohols

Synthesis

Volumn , Issue 20, 2007, Pages 3205-3210

  Yadav, J S ^a   Subba Reddy, B V ^a   Raghavendra Rao, K V ^a   Narayana Kumar, G G K S ^a  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

C alkylation; Indium reagents; Nucleophilic substitution; Propargylation

Indexed keywords

C-ALKYLATION; INDIUM REAGENTS; NUCLEOPHILIC SUBSTITUTION; PROPARGYLATION;

ALCOHOLS; ALKYLATION; INDIUM COMPOUNDS; NUCLEOPHILES; REGIOSELECTIVITY;

REACTION KINETICS;

2 (1 PHENYLHEPT 2 YNYL) 1H PYRROLE; 2 (1,3 DIPHENYLPROP 2 YNYL)FURAN; 3 (1 PHENYLHEPT 2 YNYL) 1H INDOLE; 3 (1,3 DIPHENYLPROP 2 YNYL) 1H INDOLE; 3 (1,3 DIPHENYLPROP 2 YNYL) 2 PHENYL 1H INDOLE; 3 (1,3 DIPHENYLPROP 2 YNYL) 5 NITRO 1H INDOLE; 3 (1,3 DIPHENYLPROP 2 YNYL) 9H CARBAZOLE; 3 [ 3 PHENYL 1 (2 PHENYLETHYNYL)ALLYL] 1H INDOLE; 3 [ 3 PHENYL 1 (2 PHENYLETHYNYL)ALLYL] 1H INDOLE 5 CARBONITRILE; 3 [1 (4 FLUOROPHENYL) 3 PHENYLPROP 2 YNYL] 1H INDOLE; 3 [1 (4 TOLYL)HEPT 2 YNYL] 1H INDOLE; 3 [1 (4 TOLYL)HEPT 2 YNYL] 1H INDOLE 5 CARBONITRILE; 5 BROMO 3 (1,3 DIPHENYLPROP 2 YNYL) 1H INDOLE; 5 BROMO 3 [1 [ 2 PHENYLVINYL]HEPT 2 YNYL] 1H INDOLE; 5 NITRO 3 (1 PHENYLHEPT 2 YNYL) 1H INDOLE; 5 NITRO 3 [1 (4 TOLYL)HEPT 2 YNYL] 1H INDOLE; 7 ETHYL 3 [1 [ 2 PHENYLVINYL]HEPT 2 YNYL] 1H INDOLE; CARBAZOLE DERIVATIVE; FURAN DERIVATIVE; INDIUM; INDIUM BROMIDE; INDOLE DERIVATIVE; PYRROLE DERIVATIVE; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; CATALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;

EID: 35548963275     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-990797     Document Type: Article

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