Reactivity of Benzylic Acylammonium Chlorides. A Novel Method for the Synthesis of N-Phenacylamides: Synthetic Communications: Vol 27, No 1

Synthetic Communications

An International Journal for Rapid Communication of Synthetic Organic Chemistry

Volume 27, 1997 - Issue 1

185

Views

CrossRef citations to date

Altmetric

Abstract

Tertiary amines 1 reacted with acid chlorides 2 to give corresponding benzyl chlorides and N-phenacylamides 4 . Counterion in species 3 attacked preferentially the benzylic methylene. Effect of substituents in the benzyl group on the reactivity of acylammonium chlorides 3 was investigated.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

Reactivity of Benzylic Acylammonium Chlorides. A Novel Method for the Synthesis of N-Phenacylamides

Information for

Open access

Opportunities

Help and information

Reactivity of Benzylic Acylammonium Chlorides. A Novel Method for the Synthesis of N-Phenacylamides

Abstract

Reprints and Corporate Permissions

Academic Permissions

Related research

To cite this article:

Download citation

Information for

Open access

Opportunities

Help and information

Keep up to date

Your download is now in progress and you may close this window

Login or register to access this feature