A convenient synthesis of tertiary carbinamines via N-aluminum ketimines

Article abstract of DOI:10.1080/00397919708004130

Reaction of N-unsubstituted ketimines with organoaluminum reagents prepared from allylic and propargylic halides, allows to prepare, in good yields, tertiary carbinamines with three different groups (phenyl, alkyl and α-unsaturated group) on die tertiary carbon center.

Full text of DOI:10.1080/00397919708004130

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Synthetic Communications: An
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A Convenient Synthesis of
Tertiary Carbinamines via N-
Aluminum Ketimines
a
a
Francis Barbot & Léone Miginiac
a
Laboratoire de Synthèse Organique, URA 574
CNRS , Université de Poitiers , 40, avenue du
Recteur Pineau, 86022, Poitiers, France
Published online: 22 Aug 2006.
To cite this article: Francis Barbot & Léone Miginiac (1997) A Convenient Synthesis
of Tertiary Carbinamines via N-Aluminum Ketimines, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 27:15,
2601-2614, DOI: 10.1080/00397919708004130
To link to this article: http://dx.doi.org/10.1080/00397919708004130
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