Stereoselective routes to E and Z straight-chain primary allylic amines

Article abstract of DOI:10.1080/00397919808005962

Stereoselective reduction of a triple C-C bond and chemoselective transformation of an azide function into amino group have been employed in the synthesis of straight-chain primary E and Z allylic amines from alk-2- yn-1-ols.

Full text of DOI:10.1080/00397919808005962

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Stereoselective Routes to E and
Z Straight-Chain Primary Allylic
Amines
Beata Tomassy a & Andrzej Zwierzak a
a Institute of Organic Chemistry, Technical University
(Politechnika) , Zeromskiego 116, Lodz, Poland
Published online: 15 Aug 2006.
To cite this article: Beata Tomassy & Andrzej Zwierzak (1998) Stereoselective Routes
to E and Z Straight-Chain Primary Allylic Amines, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 28:7,
1201-1214, DOI: 10.1080/00397919808005962
To link to this article: http://dx.doi.org/10.1080/00397919808005962
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