4,4,5,5-Tetraphenyl-1,3,2-dioxaborolane: A Bulky Borane for the Transition Metal Catalysed Hydroboration of Alkenes

摘要:

4,4,5,5-Tetraphenyl-1,3,2-dioxaborolane (HBBzpin, 3) has been prepared in high yield by the addition of H3B-SMe2 to benzopinacol. HBBzpin is a relatively stable solid that reacts with a variety of alkenes under catalytic conditions to give air- and chromatography-stable organoboronate esters. Reactions of vinylarenes in the presence of catalytic amounts of [Cp * IrCl2](2) gave the corresponding terminal products selectively. Addition of HBBzpin to RhCl(PPh3)(3) gave Rh(H)Cl(BzBpin)(PPh3)(2) (11) as the only new rhodium-containing product. The complex 11 has been characterized by a number of physical and analytical methods, including a single-crystal X-ray diffraction study. ((c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008).

展开

DOI:

10.1002/ejic.200701066

年份:

2008

通过文献互助平台发起求助,成功后即可免费获取论文全文。

相似文献

参考文献

引证文献

辅助模式

0

引用

文献可以批量引用啦~
欢迎点我试用!

关于我们

百度学术集成海量学术资源,融合人工智能、深度学习、大数据分析等技术,为科研工作者提供全面快捷的学术服务。在这里我们保持学习的态度,不忘初心,砥砺前行。
了解更多>>

友情链接

百度云百度翻译

联系我们

合作与服务

期刊合作 图书馆合作 下载产品手册

©2025 Baidu 百度学术声明 使用百度前必读

引用