Molecules 2006, 11(7), 523-527; doi:10.3390/11070523

[Hydroxy(tosyloxy)iodo]benzene Mediated α-Azidation of Ketones

Department of Chemistry, Kurukshetra University, Kurukshetra, Haryana, India
* Author to whom correspondence should be addressed.
Received: 20 August 2005; in revised form: 10 March 2006 / Accepted: 12 March 2006 / Published: 14 July 2006
PDF Full-text Download PDF Full-Text [62 KB, uploaded 20 June 2008 16:50 CEST]
Abstract: Reaction of various ketones with [hydroxy(tosyloxy)iodo]benzene (HTIB) followed by treatment of the α-tosyloxy ketones thus generated in situ with NaN3 offers a one-pot procedure for the synthesis of α-azido ketones. The HTIB used in this conversion may also be generated in situ by using iodosobenzene in combination with p-toluene- sulphonic acid.
Keywords: Hypervalent iodine; α-azido ketones; [hydroxy(tosyloxy)iodo]benzene; iodosobenzene.

Article Statistics

Load and display the download statistics.

Citations to this Article

Cite This Article

MDPI and ACS Style

Prakash, O.; Pannu, K.; Prakash, R.; Batra, A. [Hydroxy(tosyloxy)iodo]benzene Mediated α-Azidation of Ketones. Molecules 2006, 11, 523-527.

AMA Style

Prakash O, Pannu K, Prakash R, Batra A. [Hydroxy(tosyloxy)iodo]benzene Mediated α-Azidation of Ketones. Molecules. 2006; 11(7):523-527.

Chicago/Turabian Style

Prakash, Om; Pannu, Kamaljeet; Prakash, Richa; Batra, Anita. 2006. "[Hydroxy(tosyloxy)iodo]benzene Mediated α-Azidation of Ketones." Molecules 11, no. 7: 523-527.

Molecules EISSN 1420-3049 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert