QUANTITATIVE STUDY OF NUCLEOPHILICITY OF THIOCARBONYL GROUP IN HETEROCYCLIC-COMPOUNDS

被引：11

作者：

ARBELOT, M ^{[1
]}

GALLO, R ^{[1
]}

CHANON, M ^{[1
]}

METZGER, J ^{[1
]}

机构：

[1] ST JEROME,FAC SCI,CHIM ORG LAB A,F-13013 MARSEILLE,FRANCE

来源：

PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS | 1976年 / 1卷 / 2-3期

关键词：

D O I：

10.1080/03086647608073332

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

引用

收藏

页码：271 / 279

页数：9

相关论文

共 33 条

[1] FRONTIER CONTROL NUCLEOPHILIC REACTIVITY AND PHOTOELECTRON-SPECTROSCOPY DATA WITHIN KLOPMAN EQUATION - THIOCARBONYL GROUP
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[2] ELECTRONIC-STRUCTURE OF SULFUR DERIVATIVES .5. ELECTRONIC-SPECTRA OF THIOCARBONYL HETEROCYCLIC-COMPOUNDS
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[J]. JOURNAL OF MOLECULAR STRUCTURE, 1974, 20 (03) : 487 - 494
[3] STERIC EFFECTS IN DISPLACEMENT REACTIONS .3. THE BASE STRENGTHS OF PYRIDINE, 2,6-LUTIDINE AND THE MONOALKYLPYRIDINES
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[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1955, 77 (07) : 1723 - 1726
[4] STERIC EFFECTS IN DISPLACEMENT REACTIONS .2. THE RATES OF REACTION OF ALKYL IODIDE S WITH THE MONOALKYLPYRIDINES - STERIC STRAIN IN THE ACTIVATED COMPLEX
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[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1955, 77 (07) : 1715 - 1723
[5] Cagle F. W., 1951, J AM CHEM SOC, V73, P5628
[6] SUR LES FACTEURS DETERMINANT LA FORCE BASIQUE DE DERIVES AZOTES DES HYDROCARBURES CONJUGUES ALTERNANTS
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[7] CHAMBONNET A, 1962, THESIS MARSEILLE
[8] CHANON M, 1968, B SOC CHIM FR, P2881
[9] CHANON M, 1971, INT J SULFUR CHEM, V6, P85
[10] COTTET R, 1967, B SOC CHIM FR, P4502

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