Advanced search
Publication Cover
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 28, 1998 - Issue 21
Submit an article Journal homepage
89
Views
1
CrossRef citations to date
0
Altmetric
Original Articles

Synthesis and Structural Determination of New Potential Chiral Tridentate Ligands Derivated from 1-(R)-(+)-Camphor

Mário L.A.A. Vasconcellos Núcleo de Pesquisas de Produtos Naturais, Universidade Federal do Rio de Janeiro, Laboratório, H1–029, bloco H, Centro de Ciências da Saúde, Ilha do Fundão, 21941-590, RJ, Brazil
,
Mauro L. Mellão Núcleo de Pesquisas de Produtos Naturais, Universidade Federal do Rio de Janeiro, Laboratório, H1–029, bloco H, Centro de Ciências da Saúde, Ilha do Fundão, 21941-590, RJ, Brazil
,
Uendel G. Barreiros Núcleo de Pesquisas de Produtos Naturais, Universidade Federal do Rio de Janeiro, Laboratório, H1–029, bloco H, Centro de Ciências da Saúde, Ilha do Fundão, 21941-590, RJ, Brazil
,
Marcelo C. Branco Instituto de Química de São Carlos, Laboratório de cristalografia av., Departamento de Química e fisica molecular, Dr. Carlos Botelho, 1465-Caixa postal, 780-13560-970, São Carlos, SP, Brazil
,
Maria T.P.Gambardella Instituto de Química de São Carlos, Laboratório de cristalografia av., Departamento de Química e fisica molecular, Dr. Carlos Botelho, 1465-Caixa postal, 780-13560-970, São Carlos, SP, Brazil
,
Oduvaldo F. Ramos Núcleo de Pesquisas de Produtos Naturais, Universidade Federal do Rio de Janeiro, Laboratório, H1–029, bloco H, Centro de Ciências da Saúde, Ilha do Fundão, 21941-590, RJ, Brazil
&
Marcelo Ribeiro Núcleo de Pesquisas de Produtos Naturais, Universidade Federal do Rio de Janeiro, Laboratório, H1–029, bloco H, Centro de Ciências da Saúde, Ilha do Fundão, 21941-590, RJ, Brazil
 show all
Pages 4077-4085 | Received 15 May 1998, Published online: 16 Aug 2006
 
Sample our Physical Sciences journals, sign in here to start your FREE access for 14 days

Abstract

New alcohols 3d, 3e and 3f were efficiently prepared in enantiopure form (2 steps, 50–58%), from available 1-(R)-(+)-camphor 1. The absolute configurations were assigned by NMR and relative X-ray crystallographic analysis.

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.