AROMATIC REACTIVITY .61. REACTIVITIES AND SOLVENT ISOTOPE EFFECTS IN BASE CLEAVAGE OF TRIORGANO-SILICON, TRIORGANO-GERMANIUM, AND TRIORGANO-TIN GROUPS FROM FURAN, THIOPHENE, BENZOFURAN, AND BENZOTHIOPHEN RINGS

被引：33

作者：

EABORN, C

SECONI, G

机构：

[1] UNIV SUSSEX,SCH MOLEC SCI,BRIGHTON BN1 9QJ,SUSSEX,ENGLAND

[2] CNR,COMPOSTI CARBONIO CONTENENTI ETEROATOMI & APPLICAZIONI,I-40064 OZZANO EMILIA,ITALY

来源：

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2 | 1976年 / 08期

关键词：

D O I：

10.1039/p29760000925

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：925 / 930

页数：6

共 26 条

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[2] AROMATIC REACTIVITY .55. SOLVENT ISOTOPE-EFFECTS IN BASE CLEAVAGE OF ARYLTRIMETHYLSTANNANES IN METHANOL - EVIDENCE FOR ELECTROPHILIC ASSISTANCE BY SOLVENT [J].

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[6] ORGANOSILICON COMPOUNDS .33. ADDITIONAL SUBSTITUENT EFFECTS IN ALKALI CLEAVAGE OF BENZYLTRIMETHYLSILANES [J].

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[7] ALKALI-CLEAVAGE OF SOME CARBON-SILICON, -GERMANIUM, AND -TIN BONDS [J].

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[8] AROMATIC REACTIVITY .18. ACID CLEAVAGE OF TRIMETHYLSILYL DERIVATIVES OF DIPHENYL ETHER, DIPHENYL SULPHIDE, FURAN, THIOPHEN, BENZOTHIOPHEN, DIBENZOFURAN, DIBENZOTHIOPHEN, AND 9-ETHYLCARBAZOLE [J].

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[9] AROMATIC REACTIVITY .10. RELATIVE RATES OF CLEAVAGE OF ARYL-SILICON, ARYL-TIN, ARYL-GERMANIUM, AND ARYL-LEAD BONDS BY AQUEOUS-ETHANOLIC PERCHLORIC ACID [J].

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[10] AROMATIC REACTIVITY .35. ALKALI CLEAVAGE OF ARYLTRIMETHYLSTANNANES - AN UNUSUAL ELECTROPHILIC AROMATIC SUBSTITUTION [J].

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