Issue 8, 2017
From the journal:

New Journal of Chemistry

Tetraalkynylstannanes in the Stille cross coupling reaction: a new effective approach to arylalkynes†

Andrey S. Levashov, ORCID logo *a   Dmitrii S. Buryi,a   Olga V. Goncharova,a   Valeriy V. Konshin,a   Victor V. Dotsenkoab  and  Alexey A. Andreev‡a  

* Corresponding authors

a Department of Organic Chemistry & Technologies, Kuban State University, 149 Stavropolskaya str., 350040 Krasnodar, Russian Federation
E-mail: aslevashov@mail.ru

b Department of Chemistry, North Caucasus Federal University, 1a Pushkin str., 355009 Stavropol, Russian Federation

Abstract

The Stille-type cross coupling reaction with tetraalkynylstannanes was studied in detail for the first time. The reaction provides a simple and effective route towards a variety of arylalkynes. The advantages and limitations of the proposed procedure are discussed.

Graphical abstract: Tetraalkynylstannanes in the Stille cross coupling reaction: a new effective approach to arylalkynes

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C6NJ03905G
Article type
Paper
Submitted
13 Dec 2016
Accepted
20 Feb 2017
First published
21 Feb 2017
This article is Open Access
Creative Commons BY license

New J. Chem., 2017,41, 2910-2918

Permissions

Request permissions

Tetraalkynylstannanes in the Stille cross coupling reaction: a new effective approach to arylalkynes

A. S. Levashov, D. S. Buryi, O. V. Goncharova, V. V. Konshin, V. V. Dotsenko and A. A. Andreev, New J. Chem., 2017, 41, 2910 DOI: 10.1039/C6NJ03905G

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements