Advanced search
Publication Cover
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 29, 1999 - Issue 21
Submit an article Journal homepage
36
Views
4
CrossRef citations to date
0
Altmetric
Original Articles

Synthesis of the C2 Symmetric 1,3-Dicyclohexyl-1,3-Propanediol and Diamine Enantiomers

A. Richard Donovan Department of Chemistry, Division of Science, Murdoch University, Murdoch, Western Australia, 6150
&
Gregory H. P. Roos Chemistry Department, College of Science, Sultan Qaboos University, Box 36, Al-Khod, Sultanate of Oman, 123
Pages 3685-3692 | Received 13 Jan 1999, Accepted 29 Mar 1999, Published online: 17 Sep 2007
 
Sample our Physical Sciences journals, sign in here to start your FREE access for 14 days

Abstract

The parent C2-symmetric (R,R)- and (S,S)-1,3-dicyclohexyl-1,3-propanediols and diamines are readily obtained from the corresponding diphenyldiol precursors.

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.