One-Pot Zn/CuI/TFA-catalyzed domino three-component-carbocyclization reaction involving Biphenyl-2-carbaldehydes/Alkynes/Piperidine: Allenes-mediated construction of phenanthrenes

Journal of Organic Chemistry

Volumn 76, Issue 24, 2011, Pages 10122-10128

  Saifuddin, Mohammad ^a   Agarwal, Piyush K ^a   Kundu, Bijoy ^a  

^a CENTRAL DRUG RESEARCH INSTITUTE   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ALLENES; CARBOCYCLIZATION; CARBOCYCLIZATION REACTIONS; FUNCTIONALIZATIONS; GOOD YIELD; ONE POT; ONE-POT PROTOCOL; PROPARGYL; RING CLOSURES; THREE-COMPONENT;

ACETYLENE; ANTHRACENE;

CATALYSIS;

1,2,3 TRIMETHOXY 10 (4 METHOXYBENZYL)PHENANTHRENE; 1,2,3 TRIMETHOXY 10 (4 METHYLBENZYL)PHENANTHRENE; 1,2,3 TRIMETHOXY 10 [4 (TERT BUTYL)BENZYL]PHENANTHRENE; 10 BENZYL 1,2,3 TRIMETHOXYPHENANTHRENE; 10 BENZYL 2,3 DIMETHOXY 5 ETHOXYPHENANTHRENE; 10 BENZYL 2,3 DIMETHOXYPHENANTHRENE; 2,3 DIMETHOXY 10 (4 METHOXYBENZYL)PHENANTHRENE; 2,3 DIMETHOXY 10 (4 METHYLBENZYL)PHENANTHRENE; 2,3 DIMETHOXY 10 [4 (TERT BUTYL)BENZYL)PHENANTHRENE; 2,3 DIMETHOXY 5 ETHOXY 10 (4 METHOXYBENZYL)PHENANTHRENE; 2,3 DIMETHOXY 5 ETHOXY 10 (4 METHYLBENZYL)PHENANTHRENE; 2,3 DIMETHOXY 5 ETHOXY 10 [4 (TERT BUTYL)BENZYL]PHENANTHRENE; 2,3 DIMETHOXY 9 (4 METHYLBENZYL)PHENANTHRENE; 2,3 DIMETHOXY 9 [4 (TERT BUTYL)BENZYL]PHENANTHRENE; 9 (4 METHYLBENZYL)PHENANTHRENE; 9 [4 (TERT BUTYL)BENZYL]PHENANTHRENE; 9 BENZYL 2,3 DIMETHOXYPHENANTHRENE; 9 BENZYLPHENANTHRENE; ALDEHYDE DERIVATIVE; ALKYNE DERIVATIVE; ALLENE DERIVATIVE; AMINE; COPPER; IMINE; MESYLIC ACID; PHENANTHRENE DERIVATIVE; PIPERIDINE DERIVATIVE; TRIFLUOROACETIC ACID; TRIFLUOROMETHANESULFONIC ACID; UNCLASSIFIED DRUG; ZINC;

ARTICLE; CARBOCYCLIZATION; CATALYSIS; CYCLIZATION; CYCLOADDITION; DRUG SYNTHESIS; ELIMINATION REACTION; ISOMERIZATION; ONE POT SYNTHESIS; REACTION OPTIMIZATION; RING CLOSING METATHESIS;

ALDEHYDES; ALKADIENES; ALKYNES; CATALYSIS; COPPER; CYCLIZATION; IMINES; MAGNETIC RESONANCE SPECTROSCOPY; PHENANTHRENES; PIPERIDINES; TRIFLUOROACETIC ACID; ZINC;

EID: 84055217233     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo201942r     Document Type: Article

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