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HYDROGENOLYSIS OF ACETAL 6,8-DIOXABICYCLO[3.2.1]OCTANE BY ALUMINUM-CHLORIDE HYDRIDE - EVIDENCE FOR PREFERRED DIRECTION OF RING CLEAVAGE IN COURSE OF ALPHA-BROMINATION OF THIS ACETAL

被引：10
作者：
CLASPER, P
BROWN, RK
机构：
来源：
JOURNAL OF ORGANIC CHEMISTRY | 1972年 / 37卷 / 21期
关键词：
D O I：
10.1021/jo00986a033
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
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页码：3346 / &
相关论文
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[2]   HYDROGENOLYSIS BY ALCL3-LIALH4 OF ETHER SOLUTIONS OF CIS AND TRANS ISOMERS OF 2,4-DISUBSTITUTED-1,3-DIOXOLANES [J].
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[3]   INFLUENCE OF SUBSTITUENTS ON EASE + DIRECTION OF RING OPENING IN LIALH4-ALCL3 REDUCTIVE CLEAVAGE OF SUBSTITUTED 1,3-DIOXOLANES [J].
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CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1964, 42 (05) :990-&
[4]  
MURRAY TP, 1971, J ORG CHEM, V36, P1311
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