Issue 7, 1971
From the journal:

Journal of the Chemical Society D: Chemical Communications

Effect of substituents on the stereochemical course of Diels–Alder reaction between β-nitrostyrenes and trans,trans-1,4-diphenylbutadiene

Padam C. Jain,   Yatindra N. Mukerjee  and  Nitya Anand  

Abstract

In a study of the Diels–Alder reaction of trans,-trans-1,4-diphenylbutadiene with β-nitrostyrenes a marked stereoselectivity to phenyl “endo” adducts has been observed on introduction of electron-withdrawing substituents in the para-position of the phenyl ring of the β-nitrostyrenes.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/C29710000303
Article type
Paper

J. Chem. Soc. D, 1971, 303-304

Permissions

Request permissions

Effect of substituents on the stereochemical course of Diels–Alder reaction between β-nitrostyrenes and trans,trans-1,4-diphenylbutadiene

P. C. Jain, Y. N. Mukerjee and N. Anand, J. Chem. Soc. D, 1971, 303 DOI: 10.1039/C29710000303

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