Hypoiodous acid initiated rearrangement of tertiary propargylic alcohols to α-iodoenones

Moran, Wesley J. and Rodriguez, Arantxa (2012) Hypoiodous acid initiated rearrangement of tertiary propargylic alcohols to α-iodoenones. Organic & Biomolecular Chemistry, 10 (43). pp. 8590-8592. ISSN 1477-0520

Abstract

In the presence of an oxidant, sodium iodide is converted into hypoiodous acid which effects the rearrangement of tertiary propargylic alcohols to α-iodoenones in good yields.

Information

URI:

https://eprints.hud.ac.uk/id/eprint/15460

URI:

https://eprints.hud.ac.uk/id/eprint/15460

URI:

https://eprints.hud.ac.uk/id/eprint/15460

URI:

https://eprints.hud.ac.uk/id/eprint/15460

URI:

https://eprints.hud.ac.uk/id/eprint/15460

URI:

https://eprints.hud.ac.uk/id/eprint/15460

URI:

https://eprints.hud.ac.uk/id/eprint/15460

URI:

https://eprints.hud.ac.uk/id/eprint/15460

URI:

https://eprints.hud.ac.uk/id/eprint/15460

URI:

https://eprints.hud.ac.uk/id/eprint/15460

URI:

https://eprints.hud.ac.uk/id/eprint/15460

URI:

https://eprints.hud.ac.uk/id/eprint/15460

Title:

Hypoiodous acid initiated rearrangement of tertiary propargylic alcohols to α-iodoenones

Creators:

Moran, Wesley J. and Rodriguez, Arantxa

Identification Number:

10.1039/C2OB26360B

Official URL:

http://dx.doi.org/10.1039/C2OB26360B

Date:

October 2012

Subjects:

Q Science > Q Science (General)
Q Science > QD Chemistry

Schools:

School of Applied Sciences

Library

Item Type:

Article

Depositing User:

Date Deposited:

09 Oct 2012 09:18

Revision:

20

Last Modified:

28 Aug 2021 20:26

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