VINYLOXYBORANES AS SYNTHETIC INTERMEDIATES

被引：95

作者：

MUKAIYAM.T ^{[1
]}

INOMATA, K ^{[1
]}

MURAKI, M ^{[1
]}

机构：

[1] TOKYO INST TECHNOL, LAB ORG CHEM, MEGURO, TOKYO, JAPAN

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 1973年 / 95卷 / 03期

关键词：

D O I：

10.1021/ja00784a079

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：967 / 968

页数：2

共 16 条

[1] A FACILE REACTION OF ORGANOBORANES WITH ACROLEIN . A CONVENIENT NEW ALDEHYDE SYNTHESIS VIA HYDROBORATION
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[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1967, 89 (22) : 5709 - &
[2] OXYGEN-INDUCED REACTIONS OF ORGANOBORANES WITH INERT ALPHA,BETA-UNSATURATED CARBONYL DERIVATIVES . A CONVENIENT NEW ALDEHYDE AND KETONE SYNTHESIS VIA HYDROBORATION
BROWN, HC
KABALKA, GW
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1970, 92 (03) : 714 - &
[3] ACYL PEROXIDE AND PHOTOCHEMICAL INDUCED REACTIONS OF ORGANOBORANES WITH INERT ALPHA,BETA-UNSATURATED CARBONYL DERIVATIVES
BROWN, HC
KABALKA, GW
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1970, 92 (03) : 712 - &
[4] ALKYLATION OF DIAZOACETONITRILE AND ETHYL DIAZOACETATE BY MEANS OF ORGANOBORANES . A NEW SYNTHESIS OF NITRILES AND ESTERS
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LINKE, S
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1968, 90 (24) : 6891 - &
[5] REACTION OF ORGANOBORANES WITH DIAZO ESTERS AND DIAZO KETONES IN PRESENCE OF DEUTERIUM OXIDE . A NEW SYNTHESIS OF ALPHA-DEUTERIO- AND ALPHA,ALPHA-DIDEUTERIO ESTERS AND KETONES
HOOZ, J
GUNN, DM
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1969, 91 (22) : 6195 - &
[6] REACTION OF TRIALKYLBORANES WITH DIAZOACETONE . A NEW KETONE SYNTHESIS
HOOZ, J
LINKE, S
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1968, 90 (21) : 5936 - &
[7] HOOZ J, 1969, TETRAHEDRON LETT, P3455
[8] HOOZ J, 1969, CHEM COMMUN, V139
[9] INHIBITION OF REACTION OF ORGANOBORANES WITH ALPHA,BETA-UNSATURATED CARBONYL DERIVATIVES BY GALVINOXYL . EVIDENCE FOR A FREE-RADICAL CHAIN MECHANISM
KABALKA, GW
BROWN, HC
SUZUKI, A
HONMA, S
ARASE, A
ITOH, M
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1970, 92 (03) : 710 - &
[10] KOSTER R, 1968, ANGEW CHEM, V80, P756

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