A new pseudo C2-symmetric tertiary diamine for the enantioselective addition of MeLi to aromatic imines

Tetrahedron Asymmetry

Volumn 17, Issue 7, 2006, Pages 1045-1047

  Gille, Ségolène ^a   Cabello, Noemi ^a   Kizirian, Jean Claude ^a   Alexakis, Alexandre ^a  

^a UNIVERSITY OF GENEVA   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC COMPOUND; DIAMINE; IMINE; LITHIUM DERIVATIVE; METHYL GROUP; PSEUDOEPHEDRINE;

ADDITION REACTION; ARTICLE; CHEMICAL MODIFICATION; CHEMICAL REACTION KINETICS; COMPARATIVE STUDY; ENANTIOSELECTIVITY; PRIORITY JOURNAL; STEREOCHEMISTRY;

EID: 33646496365     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2006.03.026     Document Type: Article

References (11)

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11. 1H NMR spectrum of this crude was analyzed to determine the conversion of the reaction. Finally, purification by silica gel column chromatography gave pure amines 4a-f already fully characterized in Ref. 2b.