NEW STEREOSPECIFIC CROSS-COUPLING BY THE PALLADIUM-CATALYZED REACTION OF 1-ALKENYLBORANES WITH 1-ALKENYL OR 1-ALKYNYL HALIDES

被引：1896

作者：

MIYAURA, N ^{[1
]}

YAMADA, K ^{[1
]}

SUZUKI, A ^{[1
]}

机构：

[1] HOKKAIDO UNIV, FAC ENGN, SAPPORO, HOKKAIDO 060, JAPAN

来源：

TETRAHEDRON LETTERS | 1979年 / 20卷 / 36期

关键词：

D O I：

10.1016/S0040-4039(01)95429-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The representative (E)-1-alkenyldisiamylboranes and (E)-1-alkenyl-1,3,2-benzodioxaboroles readily obtainable via hydroboration of 1-alkynes react with 1-alkenyl halides or 1-alkynyl halides in the presence of a catalytic amount of tetrakis(triphenylphosphine)palladium and base to give corresponding conjugated (E)-dienes or (E)-enynes with high regio- and stereospecificity in good yields, respectively. © 1979.

引用

页码：3437 / 3440

页数：4

共 16 条

[1] NOVEL STEREOSPECIFIC ALKENYL-ALKENYL CROSS-COUPLING BY A PALLADIUM-CATALYZED OR NICKEL-CATALYZED REACTION OF ALKENYLALANES WITH ALKENYL HALIDES
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[6] PALLADIUM-CATALYZED CONJUGATED DIENE SYNTHESIS FROM VINYLIC HALIDES AND OLEFINIC COMPOUNDS
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HECK, RF
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[7] MERCURY IN ORGANIC-CHEMISTRY .7. CONVENIENT SYNTHESIS OF SYMMETRICAL CONJUGATED DIENES AND POLYENES
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[J]. JOURNAL OF ORGANIC CHEMISTRY, 1976, 41 (13) : 2241 - 2246
[8] STEREOSELECTIVE SYNTHESIS OF CONJUGATED TRANS-ENYNES READILY CONVERTIBLE INTO CONJUGATED CIS,TRANS-DIENES AND ITS APPLICATION TO SYNTHESIS OF PHEROMONE BOMBYKOL
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[J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1973, (22) : 874 - 875
[9] NEGISHI E, 1972, J CHEM SOC CHEM COMM, P606
[10] STEREOSELECTIVE SYNTHESIS OF CIS-ALKENYLBORANES
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LEW, G
YOSHIDA, T
[J]. JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1975, 92 (01) : C4 - C6

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