Direct, one-pot reductive alkylation of anilines with functionalized acetals mediated by triethylsilane and tfa. straightforward route for unsymmetrically substituted ethylenediamine

Journal of Organic Chemistry

Volumn 76, Issue 2, 2011, Pages 704-707

  Righi, Marika ^a   Bedini, Annalida ^a   Piersanti, Giovanni ^a   Romagnoli, Federica ^a   Spadoni, Gilberto ^a  

^a UNIVERSITY OF URBINO   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ETHYLENE DIAMINE; FUNCTIONALIZED; MILD REACTION CONDITIONS; N-ALKYLATION; ONE POT; ONE-POT PROCEDURES; REDUCTIVE ALKYLATION; ROOM TEMPERATURE; SECONDARY AROMATIC AMINES; SYNTHETIC APPROACH; TRIETHYLSILANE;

AMINES; FUNCTIONAL GROUPS; HYDROTHERMAL SYNTHESIS;

ALKYLATION;

ACETAL DERIVATIVE; ACETAMIDE; ANILINE DERIVATIVE; CARBAMIC ACID DERIVATIVE; ETHYLENEDIAMINE; SILANE DERIVATIVE;

ALKYLATION; AMINATION; ARTICLE; CHEMICAL STRUCTURE; ONE POT SYNTHESIS; REDUCTION;

ACETALS; ALKYLATION; ANILINE COMPOUNDS; CATALYSIS; ETHYLENEDIAMINES; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; OXIDATION-REDUCTION; SILANES; TRIFLUOROACETIC ACID;

EID: 78651519487     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo102109f     Document Type: Article

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