Palladium-catalyzed cross-coupling of 3-iodobut-3-enoic acid with organometallic reagents.: Synthesis of 3-substituted but-3-enoic acids

被引：21

作者：

Abarbri, M

Parrain, JL

Kitamura, M

Noyori, R

Duchêne, A

机构：

[1] Fac Sci Tours, Lab Physicochim Interfaces & Milieux React, F-37200 Tours, France

[2] Fac Sci & Tech St Jerome, Lab Synth Organ, CNRS, F-13397 Marseille 20, France

[3] Nagoya Univ, Dept Chem, Chikusa Ku, Nagoya, Aichi 4648602, Japan

[4] Nagoya Univ, Res Ctr Mat Sci, Chikusa Ku, Nagoya, Aichi 4648602, Japan

来源：

JOURNAL OF ORGANIC CHEMISTRY | 2000年 / 65卷 / 22期

关键词：

D O I：

10.1021/jo0007579

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

3-Substituted but-3-enoic acids were obtained in good yields under mild experimental conditions by palladium-catalyzed cross-coupling of 3-iodobut-3-enoic acid with organozinc or organotin compounds using PdCl2(MeCN)(2) as catalyst and DMF as solvent.

引用

页码：7475 / 7478

页数：4

共 46 条

[1]

Abarbri M, 1996, SYNTHESIS-STUTTGART, P82

[2]

ABE Y, 1983, CHEM PHARM BULL, V31, P4346

[3] A CONVENIENT SYNTHESIS OF PROTECTED E-ENYNALS VIA CROSS COUPLING OF VINYLTIN ACETALS WITH BROMOALKYNES [J].