The Reduction of Azides with Borohydride Supported on an Ion Exchange Resin

George W. Kabalka Departments of Chemistry and Radiology, University of Tennessee, Knoxville, TN, 37996-1600

Prakash P. Wadgaonkar Departments of Chemistry and Radiology, University of Tennessee, Knoxville, TN, 37996-1600

Narayana Chatla Departments of Chemistry and Radiology, University of Tennessee, Knoxville, TN, 37996-1600

Abstract

Borohydride supported on an ion exchange resin in methanol reduced aryl azides and arylsulfonyl azides to the corresponding aromatic amines and aryl sulfonamides in excellent yields. The isolation of pure products by simple filtration and evaporation is an important feature of this method.

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.

The Reduction of Azides with Borohydride Supported on an Ion Exchange Resin

Information for

Open access

Opportunities

Help and information

The Reduction of Azides with Borohydride Supported on an Ion Exchange Resin

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