Issue 9, 1989
From the journal:

Journal of the Chemical Society, Chemical Communications

The stereochemistry of a substitution reaction via an episelenonium ion: retention by a 2-pyridylseleno group versus scrambling by a phenylseleno group

Akio Toshimitsu,   Masaaki Ito  and  Sakae Uemura  

Abstract

The first example of retention of configuration during substitution on a carbon atom situated β to an arylseleno group was discovered when using a 2-pyridylseleno (2-PySe) group.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/C39890000530
Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 530-531

Permissions

Request permissions

The stereochemistry of a substitution reaction via an episelenonium ion: retention by a 2-pyridylseleno group versus scrambling by a phenylseleno group

A. Toshimitsu, M. Ito and S. Uemura, J. Chem. Soc., Chem. Commun., 1989, 530 DOI: 10.1039/C39890000530

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