REMARKABLY FACILE REDUCTIVE OPENING OF TETRAHYDROFURAN AND RELATED ETHERS BY LITHIUM TRI-TERT BUTOXYALUMINOHYDRIDE IN PRESENCE OF TRIETHYLBORANE

被引：40

作者：

BROWN, HC

KRISHNAM.S

COLEMAN, RA

机构：

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 1972年 / 94卷 / 05期

关键词：

D O I：

10.1021/ja00760a059

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

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页码：1750 / &

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[2] THE REACTION OF LITHIUM ALUMINUM HYDRIDE WITH ALCOHOLS - LITHIUM TRI-TERT-BUTOXY-ALUMINOHYDRIDE AS A NEW SELECTIVE REDUCING AGENT
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[3] SELECTIVE REDUCTIONS .7. REACTION OF LITHIUM TRIMETHOXYALUMINOHYDRIDE WITH SELECTED ORGANIC COMPOUNDS CONTAINING REPRESENTATIVE FUNCTIONAL GROUPS
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[4] REACTION OF B-ALKYL-9-BORABICYCLO[3.3.1]NONANES WITH CARBON MONOXIDE IN PRESENCE OF LITHIUM TRI-T-BUTOXYALUMINOHYDRIDE - CONVERSION OF FUNCTIONALLY SUBSTITUTED OLEFINS INTO ALDEHYDES VIA HYDROBORATION
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[5] BROWN HC, 1963, ISRAEL J CHEM, V1, P430
[6] REDUCTIVE RING-CLEAVAGE OF TETRAHYDROFURANS BY DIBORANE
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