Get 20M+ Full-Text Papers For Less Than $1.50/day. Start a 7-Day Trial for You or Your Team.

Learn More →

Pd-catalysed cross coupling of terminal alkynes to diynes in the absence of a stoichiometric additive.

Pd-catalysed cross coupling of terminal alkynes to diynes in the absence of a stoichiometric... An efficient, room temperature procedure for the cross-coupling of a range of terminal alkynes, using standard Sonogashira cross-coupling conditions (Pd/Cu) is presented. At higher reaction temperatures, head-to-tail or head-to-head dimerisation affords 1,3- and 1,4-disubstituted enynes, respectively as minor products. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Chemical Communications Pubmed

Pd-catalysed cross coupling of terminal alkynes to diynes in the absence of a stoichiometric additive.

Chemical Communications , Volume (5): -628 – Jun 10, 2003

Pd-catalysed cross coupling of terminal alkynes to diynes in the absence of a stoichiometric additive.


Abstract

An efficient, room temperature procedure for the cross-coupling of a range of terminal alkynes, using standard Sonogashira cross-coupling conditions (Pd/Cu) is presented. At higher reaction temperatures, head-to-tail or head-to-head dimerisation affords 1,3- and 1,4-disubstituted enynes, respectively as minor products.

Loading next page...
 
/lp/pubmed/pd-catalysed-cross-coupling-of-terminal-alkynes-to-diynes-in-the-5KwSHWzVb5

References (9)

ISSN
1359-7345
DOI
10.1039/b212430k
pmid
12669860

Abstract

An efficient, room temperature procedure for the cross-coupling of a range of terminal alkynes, using standard Sonogashira cross-coupling conditions (Pd/Cu) is presented. At higher reaction temperatures, head-to-tail or head-to-head dimerisation affords 1,3- and 1,4-disubstituted enynes, respectively as minor products.

Journal

Chemical CommunicationsPubmed

Published: Jun 10, 2003

There are no references for this article.