Issue 8, 1986
From the journal:

Journal of the Chemical Society, Chemical Communications

Asymmetric Diels–Alder reactions: (S)-(+)-[(η5-C5H5)Fe(CO)(PPh3)COCH[double bond, length half m-dash]CH2] as a chiral acrylate dienophile equivalent

Stephen G. Davies  and  Jonathan C. Walker  

Abstract

The zinc chloride-mediated Diels–Alder reaction between (S)-(+)-[(η5-C5H5)Fe(CO)(PPh3)COCH[double bond, length half m-dash]CH2] and cyclopentadiene yielded (2S)-(–)-bicyclo[2.2.1]hept-5-ene-2-endo-carboxylic acid which was converted into the corresponding optically pure iodolactone.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/C39860000609
Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 609-610

Permissions

Request permissions

Asymmetric Diels–Alder reactions: (S)-(+)-[(η5-C5H5)Fe(CO)(PPh3)COCH[double bond, length half m-dash]CH2] as a chiral acrylate dienophile equivalent

S. G. Davies and J. C. Walker, J. Chem. Soc., Chem. Commun., 1986, 609 DOI: 10.1039/C39860000609

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements