METHYLCOPPER INDUCED COUPLING OF DIALKENYLCHLOROBORANES - NEW PROCEDURE FOR STEREOSELECTIVE SYNTHESIS OF (E,E)-1,3-DIENES

被引：31

作者：

YAMAMOTO, Y ^{[1
]}

YATAGAI, H ^{[1
]}

MORITANI, I ^{[1
]}

机构：

[1] OSAKA UNIV,FAC ENGN SCI,DEPT CHEM,TOYONAKA 560,OSAKA,JAPAN

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 1975年 / 97卷 / 19期

关键词：

D O I：

10.1021/ja00852a061

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：5606 / 5607

页数：2

共 14 条

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[2] REACTION OF REPRESENTATIVE ALKYNES WITH MONOCHLOROBORANE DIETHYL ETHERATE - SIMPLE CONVENIENT SYNTHESIS OF DIALKENYLCHLOROBORANES VIA HYDROBORATION
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[3] BROWN HC, 1961, J AM CHEM SOC, V83, P1001, DOI 10.1021/ja01465a062
[4] COPPER-INDUCED COUPLING OF VINYL HALIDES - STEREOCHEMISTRY OF ULLMANN REACTION
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[5] REACTION BETWEEN TRIALKYLBORANES AND COPPER(II) SALTS - UNUSUAL ELECTTRON-TRANSFER OXIDATION-REDUCTION
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[J]. JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1971, 31 (03) : 421 - &
[6] LAPPERT MF, 1967, CHEMISTRY BORON ITS, P443
[7] ORGANOBORANES .10. A FAST REACTION OF ORGANOBORANES WITH MERCURIC ACETATE - A CONVENIENT PROCEDURE FOR CONVERSION OF TERMINAL OLEFINS INTO ALKYLMERCURIC SALTS VIA HYDROBORATION-MERCUTRATION
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[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1970, 92 (08) : 2467 - +
[8] REACTION OF 2-ALKENYL-1,3,2-BENZODIOXABOROLES WITH MERCURIC ACETATE - CONVENIENT STEREOSPECIFIC PROCEDURE FOR CONVERSION OF ALKYNES INTO ALKENYLMERCURIC SALTS
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GUPTA, SK
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[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1972, 94 (12) : 4371 - &
[9] HIGHLY STEREOSELECTIVE AND GENERAL SYNTHESIS OF CONJUGATED TRANS,TRANS-DIENES AND TRANS-ALKYL KETONES VIA HYDROBORATION
NEGISHI, E
YOSHIDA, T
[J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1973, (17) : 606 - 607
[10] VINYL ORGANOCOPPER COMPOUNDS .2. DEUTEROLYSIS, IODOLYSIS, COUPLING AND ALKYLATION BY STEREOSPECIFIC ADDITION OF VINYL COPPER DERIVATIVES
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[J]. JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1974, 77 (02) : 269 - 279

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