ALKYLATION ORIENTATION RULES IN CONJUGATE ADDITION OF GRIGNARD-REAGENTS TO NITROPYRROLE AND NITROTHIOPHENE SYSTEMS

被引：17

作者：

BALLINI, R ^{[1
]}

BARTOLI, G ^{[1
]}

BOSCO, M ^{[1
]}

DALPOZZO, R ^{[1
]}

MARCANTONI, E ^{[1
]}

机构：

[1] UNIV BOLOGNA,DEPARTIMENTO CHIM ORGAN,I-40136 BOLOGNA,ITALY

来源：

TETRAHEDRON | 1988年 / 44卷 / 20期

关键词：

D O I：

10.1016/S0040-4020(01)89831-8

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：6435 / 6440

页数：6

共 22 条

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[5] SELECTIVITY OF ATTACK IN NUCLEOPHILIC ALKYLATION OF NITROARENES WITH GRIGNARD-REAGENTS - REACTIVITY OF SOME SUBSTITUTED NITROBENZENES AND NITRONAPHTHALENES
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[8] 2-NITRO-THIOPHENE,3-NITRO-THIOPHENE,2,4-DINITRO-THIOPHENE, AND 2,5-DINITROTHIOPHENE
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[9] SUBSTITUENT EFFECTS IN HETEROCYCLIC RINGS - ELECTRON-SPIN RESONANCE STUDY OF SOME 5-SUBSTITUTED 2-THIENYL NITROXIDES AND NITRO-ANIONS
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[J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1974, (10): : 1195 - 1198
[10] GRONOWITZ S, 1980, CHEM SCRIPTA, V15, P145

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