A convenient one-pot synthesis of cyclohexenic primary amines

Article abstract of DOI:10.1080/00397919808004433

The reaction between Grignard reagents prepared from allylic or propargylic halides and the N-phenylsulfenimine derived from the heptane- 2,6-dione affords primary 1-alkenyl (or alkynyl)-3-methylcyclohex-2-enamines in good yields.

Full text of DOI:10.1080/00397919808004433

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A Convenient One-Pot
Synthesis of Cyclohexenic
Primary Amines
a
a
Francis Barbot , Mohand Aidene & Léone
a
Miginiac
a
Laboratoire de Synthèse Organique , URA 574
CNRS, Université de Poitiers 40 , avenue du
Recteur Pineau, 86022, Poitiers, France
Published online: 23 Aug 2006.
To cite this article: Francis Barbot , Mohand Aidene & Léone Miginiac (1998)
A Convenient One-Pot Synthesis of Cyclohexenic Primary Amines, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 28:17, 3279-3289, DOI: 10.1080/00397919808004433
To link to this article: http://dx.doi.org/10.1080/00397919808004433
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