Issue 16, 1997
From the journal:

Chemical Communications

Palladium catalysed alkylative dimerization between pronucleophiles and vinyltins

Itaru Nakamura,   Naofumi Tsukada,   Mohammad Al-Masum  and  Yoshinori Yamamoto  

Abstract

In the presence of catalytic amounts of Pd 2 (dba) 3 ·CHCl 3 and dppb, the reaction of pronucleophiles 1 with vinyltins 2 gives the corresponding alkylative dimerization products of the vinyl group, 1,4-disubstituted butene derivatives 3, in good to high yields.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/A703463F
Article type
Paper

Chem. Commun., 1997, 1583-1584

Permissions

Request permissions

Palladium catalysed alkylative dimerization between pronucleophiles and vinyltins

I. Nakamura, N. Tsukada, M. Al-Masum and Y. Yamamoto, Chem. Commun., 1997, 1583 DOI: 10.1039/A703463F

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.

Social activity

Spotlight

Advertisements