Advanced search
Publication Cover
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 12, 1982 - Issue 9
Submit an article Journal homepage
34
Views
6
CrossRef citations to date
0
Altmetric
Original Articles

A Direct Approach to the cis-1-Octalone System. 2-Carbomethoxy-2-Cyclohexenone as a Dienophile

Hsing-Jang Liu Department of Chemistry, University of Alberta Edmonton, Alberta, Canada, T6G 2G2
&
Teng Ko Ngooi Department of Chemistry, University of Alberta Edmonton, Alberta, Canada, T6G 2G2
Pages 715-722 | Published online: 05 Dec 2006
 
Sample our Physical Sciences journals, sign in here to start your FREE access for 14 days

Abstract

Under stannic chloride catalysis, 2-carbo-methoxy-2-cyclohexenone (1) was found to undergo Diels-Alder reaction with a variety of dienes to give directly the cis-1-octalone system possessing a functionalized substituent at the angular position.

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.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.