Epoxidation of 1,4-Diaroyl Ethene Derivatives in the Presence of UHP or H2O2 : Synthetic Communications: Vol 40, No 21

Synthetic Communications

An International Journal for Rapid Communication of Synthetic Organic Chemistry

Volume 40, 2010 - Issue 21

166

Views

CrossRef citations to date

Altmetric

Abstract

Hydrogen peroxide (H₂O₂) or urea–hydrogen peroxide (UHP) in basic media react with carbon–carbon double bonds of 1,4-diaroyl ethenes to produce the corresponding epoxides.

Keywords:

ACKNOWLEDGMENT

This study was supported in part by the Research Committee of the University of Guilan.

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.

Epoxidation of 1,4-Diaroyl Ethene Derivatives in the Presence of UHP or H₂O₂

Information for

Open access

Opportunities

Help and information

Epoxidation of 1,4-Diaroyl Ethene Derivatives in the Presence of UHP or H2O2

Abstract

ACKNOWLEDGMENT

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

Epoxidation of 1,4-Diaroyl Ethene Derivatives in the Presence of UHP or H₂O₂