Synthesis of acrylonitriles through an FeCl 3-catalyzed domino propargylic substitution/aza-Meyer-Schuster rearrangement sequence

Chemistry - A European Journal

Volumn 18, Issue 21, 2012, Pages 6453-6456

  Hao, Lu ^a   Wu, Feng ^a   Ding, Zong Cang ^a   Xu, Su Xia ^a   Ma, Yan Li ^a   Chen, Li ^a   Zhan, Zhuang Ping ^a  

^a XIAMEN UNIVERSITY   (China)

Author keywords

acrylonitriles; cyanides; domino reactions; iron; propargylic substitution; rearrangement

Indexed keywords

ACRYLONITRILES; CYANATION REACTION; DOMINO REACTIONS; NONTOXIC CYANIDES; PROPARGYLIC ALCOHOLS; REARRANGEMENT; REARRANGEMENT PROCESS;

ALCOHOLS; CYANIDES; IRON; REACTION KINETICS;

CATALYSIS;

ACRYLONITRILE; CHLORIDE; FERRIC CHLORIDE; FERRIC ION; HETEROCYCLIC COMPOUND; NAPHTHYRIDINE DERIVATIVE; QUINOLONE DERIVATIVE; TOSUFLOXACIN; TRIMETHYLSILYL DERIVATIVE;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; SYNTHESIS;

ACRYLONITRILE; AZA COMPOUNDS; CATALYSIS; CHLORIDES; FERRIC COMPOUNDS; FLUOROQUINOLONES; MOLECULAR STRUCTURE; NAPHTHYRIDINES; TRIMETHYLSILYL COMPOUNDS;

EID: 84861153820     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201200763     Document Type: Article

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