PALLADIUM(0)-CATALYZED HYDROBORATION OF 1-BUTEN-3-YNES - PREPARATION OF ALLENYLBORANES

被引：80

作者：

MATSUMOTO, Y

NAITO, M

HAYASHI, T

机构：

[1] HOKKAIDO UNIV,CATALYSIS RES CTR,KITA KU,SAPPORO,HOKKAIDO 060,JAPAN

[2] HOKKAIDO UNIV,GRAD SCH PHARMACEUT SCI,KITA KU,SAPPORO,HOKKAIDO 060,JAPAN

来源：

ORGANOMETALLICS | 1992年 / 11卷 / 07期

关键词：

D O I：

10.1021/om00043a075

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Reaction of 2-substituted 1-buten-3-ynes (CH2=CR-C=CH) with catecholborane in the presence of a palladium catalyst bearing a monodentate phosphine ligand such as PPh3 or PPh2(C6F5) proceeded in a 1,4-fashion to give (3-substituted 1,2-butadienyl)-1,3,2-benzodioxaboroles (CH3(R)C=C=CH(BO2C6H4)). Reaction of the allenylboranes with benzaldehyde gave the corresponding homopropargyl alcohols.

引用

页码：2732 / 2734

页数：3

共 27 条

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