HYDROBORATION .3. THE REDUCTION OF ORGANIC COMPOUNDS BY DIBORANE, AN ACID-TYPE REDUCING AGENT

被引：292

作者：

BROWN, HC

RAO, BCS

机构：

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 1960年 / 82卷 / 03期

关键词：

D O I：

10.1021/ja01488a045

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

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页码：681 / 686

页数：6

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[2] THE HYDROBORATION OF ACETYLENES - A CONVENIENT CONVERSION OF INTERNAL ACETYLENES TO CIS OLEFINS OF HIGH PURITY AND OF TERMINAL ACETYLENES TO ALDEHYDES
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[5] HYDROBORATION .1. THE REACTION OF OLEFINS WITH SODIUM BOROHYDRIDE ALUMINUM CHLORIDE - A CONVENIENT ROUTE TO ORGANOBORANES AND THE ANTI-MARKOWNIKOFF HYDRATION OF OLEFINS
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[6] SELECTIVE REDUCTIONS WITH DIBORANE, AN ACIDIC-TYPE REDUCING AGENT
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[7] ADDITION COMPOUNDS OF THE ALKALI METAL HYDRIDES .9. THE REACTION OF LEWIS ACIDS OF BORON WITH SODIUM HYDRIDE AND BOROHYDRIDE
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[9] REDUCTION OF ALDEHYDES, KETONES AND ACID CHLORIDES BY SODIUM BOROHYDRIDE
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[10] LITHIUM ALUMINUM HYDRIDE, ALUMINUM HYDRIDE AND LITHIUM GALLIUM HYDRIDE, AND SOME OF THEIR APPLICATIONS IN ORGANIC AND INORGANIC CHEMISTRY
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