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

doi:10.1080/00397919208020849

Journal ArticleDOI

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

Alain Guy, +1 more

- 01 Mar 1992 -

Synthetic Communications

- Vol. 22, Iss: 6, pp 853-857

TLDR

In this article, a method for the preparation of N-Benzyl allylamines is described, where Selenophenol generated in catalytic quantities from diphenyldiselenide and sodium borohydride leads to reductive amination of allylamine by substituted benzaldehydes.

About:

This article is published in Synthetic Communications.The article was published on 1992-03-01. It has received 6 citations till now. The article focuses on the topics: Reductive amination & Sodium borohydride.

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DOI

Protection for the Amino Group

Peter G. M. Wuts, +1 more

Journal ArticleDOI

Ruthenium-Catalyzed Allylic Substitution of Cyclic Allyl Carbonates with Nucleophiles. Stereoselectivity and Scope of the Reaction

Yasuhiro Morisaki, +2 more

- 13 Oct 1999 -

Organometallics

TL;DR: In this article, the first investigation of the stereochemical course of the ruthenium-catalyzed allylic substitution reaction with nucleophiles was carried out, in which the reaction proceeds with an overall retention of configuration.

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Journal ArticleDOI

The influence of benzylic protection and allylic substituents on the CuCl-TMEDA catalyzed rearrangement of N-allyl-N-benzyl-2,2-dihaloamides to γ-lactams. Application to the stereoselective synthesis of pilolactam

Franco Ghelfi, +10 more

- 30 Apr 1999 -

Tetrahedron

TL;DR: A number of N-benzylic protecting groups and allylic substituents have been investigated for the rearrangement, promoted by CuCl-TMEDA, of Nallyl-2,2-dihaloamides to 3,4-disubstituted γ-lactams.

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Journal ArticleDOI

Nitrones in Organic Synthesis. Synthesis of Secondary Allyl Amines

Alessandro Dondoni, +3 more

- 01 Oct 1994 -

Synthetic Communications

TL;DR: In this article, the N-benzyl allyl amines have been reduced to the corresponding N-bromide amines by adding vinyl organomagnesium bromide to give the allyl hydroxylamines.

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Reference EntryDOI

Advances in the Chemistry of Amino and Nitro Compounds

Gerhard V. Boyd

- 15 Dec 2009 -

Patai's Chemistry of Functional Groups

TL;DR: Amino compounds and nitro compounds with nucleophile reactions were studied in this paper, where the authors presented advances in chemistry of amino and Nitro compounds and showed that amino compounds can be synthesized with nucleophase reactions.

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