REDUCTIVE OPENING OF SUGAR EPOXIDES BY DIBORANE-BOROHYDRIDE ION

被引：14

作者：

FU, YL ^{[1
]}

BOBEK, M ^{[1
]}

机构：

[1] NEW YORK STATE DEPT HLTH,ROSWELL PK MEM INST,GRACE CANC DRUG CTR,DEPT EXPTL THERAPEUT,BUFFALO,NY 14263

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1980年 / 45卷 / 19期

关键词：

D O I：

10.1021/jo01307a021

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：3836 / 3840

页数：5

共 30 条

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[2] BESSIERE.Y, 1971, TETRAHEDRON LETT, P621
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[8] REACTION OF DIBORANE IN TETRAHYDROFURAN WITH STYRENE OXIDE AND RELATED EPOXIDES IN PRESENCE OF BORON TRIFLUORIDE . A CONVENIENT ANTI-MARKOVNIKOV REDUCTIVE OPENING OF SUCH EPOXIDES
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[9] BOROHYDRIDE-CATALYZED REACTION OF DIBORANE WITH EPOXIDES . ANTI-MARKOVNIKOV OPENING OF TRISUBSTITUTED EPOXIDES
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[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1968, 90 (10) : 2686 - &
[10] SELECTIVE REDUCTIONS .15. REACTION OF DIBORANE IN TETRAHYDROFURAN WITH SELECTED ORGANIC COMPOUNDS CONTAINING REPRESENTATIVE FUNCTIONAL GROUPS
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