Carboxylates as pronucleophiles in the phosphine-catalyzed gamma-addition reaction

Authors
Alvarez-Ibarra, C Csaky, AG de la Oliva, CG
Citation
C. Alvarez-ibarra et al., Carboxylates as pronucleophiles in the phosphine-catalyzed gamma-addition reaction, TETRAHEDR L, 40(48), 1999, pp. 8465-8467
Citations number
10
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
8465 - 8467
Database
ISI
SICI code
0040-4039(19991126)40:48<8465:CAPITP>2.0.ZU;2-W
Abstract
Carboxylates have been used as pronucleophiles in the phosphine-catalyzed g amma-addition reaction to alkynes bearing electron-withdrawing groups (Tros t's reaction) giving rise to functionalized allyl carboxylates. (C) 1999 El sevier Science Ltd. All rights reserved.