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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 22, 1992 - Issue 6
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Original Articles

Synthesis of N-Benzyl Allylamnes by Reductive Amination with Selenophenol Generated Catalytically

A. Guy Conservatoire National des Arts et Metiers—Laboratoire de Chimie Organique, URA, 1103, 292, rue Saint-Martin, 75141, PARIS, Cedex, 03
&
J. F. Barbetti Conservatoire National des Arts et Metiers—Laboratoire de Chimie Organique, URA, 1103, 292, rue Saint-Martin, 75141, PARIS, Cedex, 03
Pages 853-857 | Received 27 Sep 1991, Published online: 23 Sep 2006

Citations (7)

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Read on this site (1)

A. Dondoni, F.L. Merchán, P. Merino & T. Tejero. (1994) Nitrones in Organic Synthesis. Synthesis of Secondary Allyl Amines. Synthetic Communications 24:18, pages 2551-2555.
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Articles from other publishers (6)

. 2014. Greene's Protective Groups in Organic Synthesis. Greene's Protective Groups in Organic Synthesis 895 1193 .
Jocelyn Wills. (2015) Innovation in a Cold [War] Climate : Engineering Peace with the American Military–Industrial Complex . Enterprise & Society 12:1, pages 120-174.
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G. V. Boyd. 2009. PATAI'S Chemistry of Functional Groups. PATAI'S Chemistry of Functional Groups.
Yasuhiro Morisaki, Teruyuki Kondo & Take-aki Mitsudo. (1999) Ruthenium-Catalyzed Allylic Substitution of Cyclic Allyl Carbonates with Nucleophiles. Stereoselectivity and Scope of the Reaction. Organometallics 18:23, pages 4742-4746.
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Franco Ghelfi, Franco Bellesia, Luca Forti, Gianluca Ghirardini, Romano Grandi, Emanuela Libertini, Maria C Montemaggi, Ugo M Pagnoni, Adriano Pinetti, Laurent De Buyck & Andrew F Parsons. (1999) The influence of benzylic protection and allylic substituents on the CuCl-TMEDA catalyzed rearrangement of N-allyl-N-benzyl-2,2-dihaloamides to ?-lactams. Application to the stereoselective synthesis of pilolactam. Tetrahedron 55:18, pages 5839-5852.
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A. GUY & J. F. BARBETTI. (2010) ChemInform Abstract: Synthesis of N‐Benzylallylamines by Reductive Amination with Selenophenol Generated Catalytically.. ChemInform 23:35.
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