The nickel and palladium catalysed stereoselective cross coupling of cyclopropyl nucleophiles with aryl halides

被引：22

作者：

de Lang, RJ ^{[1
]}

Brandsma, L ^{[1
]}

机构：

[1] Univ Utrecht, Dept Preparat Organ Chem, NL-3584 CH Utrecht, Netherlands

来源：

SYNTHETIC COMMUNICATIONS | 1998年 / 28卷 / 02期

关键词：

D O I：

10.1080/00397919808005715

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The reaction of 2-phenylcyclopropylzinc chloride with some substituted (het)aryl halides gave the corresponding coupling products with goad yields and stereoselectivities under the influence of a catalytic amount of Pd(PPh3)(4). Other Ni- and Pd-catalysts were less efficient. Alkyl-substituted cyclopropyl nucleophiles gave lower yields.

引用

页码：225 / 232

页数：8

共 14 条

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