Highly regioselective palladium-catalyzed condensation of terminal acetylenes with 2,5-diiodobenzoic acid

Authors
Balavoine, F Madec, D Mioskowski, C
Citation
F. Balavoine et al., Highly regioselective palladium-catalyzed condensation of terminal acetylenes with 2,5-diiodobenzoic acid, TETRAHEDR L, 40(48), 1999, pp. 8351-8354
Citations number
7
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
40
Issue
48
Year of publication
1999
Pages
8351 - 8354
Database
ISI
SICI code
0040-4039(19991126)40:48<8351:HRPCOT>2.0.ZU;2-W
Abstract
Palladium-catalyzed coupling reactions between terminal alkynes and 2,5-dii odobenzoic acid have been shown to be highly regioselective, giving a rapid and efficient route for the synthesis of disymmetric 2,5-bis ethynyl benzo ic acid derivatives. (C) 1999 Elsevier Science Ltd. All rights reserved.