Reactivity of benzylic acylammonium chlorides. A novel method for the synthesis of N-phenacylamides

Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/21794

Title:	Reactivity of benzylic acylammonium chlorides. A novel method for the synthesis of N-phenacylamides
Authors:	Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü. Coşkun, Necdet Tirli, Fatma 7004177880 6505555336
Keywords:	Chemistry Ions
Issue Date:	1997
Publisher:	Taylor & Francis
Citation:	Coşkun, N. ve Tirli, F. (1997). "Reactivity of benzylic acylammonium chlorides. A novel method for the synthesis of N-phenacylamides". Synthetic Communications, 27(1), 1-9.
Abstract:	Tertian amines reacted with acid chlorides to give corresponding benzyl chlorides and N-phenacylamides Counterion in species attacked preferentially the benzylic methylene. Effect of substituents in the benzyl group on the reactivity. of acylammonium chlorides was investigated.
URI:	https://doi.org/10.1080/00397919708004799 https://www.tandfonline.com/doi/abs/10.1080/00397919708004799 http://hdl.handle.net/11452/21794
ISSN:	0039-7911
Appears in Collections:	Scopus Web of Science

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