1. |
Bibliographie Néerlandaise |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 72,
Issue 3,
1953,
Page 183-184
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ISSN:0165-0513
DOI:10.1002/recl.19530720302
出版商:WILEY‐VCH Verlag
年代:1953
数据来源: WILEY
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2. |
The effect of ortho methyl groups on the methylsulphonyl group, compared with their influence on the nitro group: (Properties of the sulphonyl group XXXIII |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 72,
Issue 3,
1953,
Page 185-194
H. Kloosterziel,
H. J. Backer,
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摘要:
Abstract4‐Methylsulphonyl‐3,5‐xylenol has been prepared by a series of reactions involving thiocyanation, reduction with LiAlH4, methylation, and oxidation. The methylsulphonyl group exerts a negative mesomeric effect, which, however, is not hindered by ortho methyl groups. The spectrum as well as the ionization constant prove this. For the latter property, additivity of Hammett's σ‐constants for groups in the 3, 4, and 5 positions was taken as a criterion. For sulphur, as a second‐row element, coplanarity of its SO‐valencies and the benzene nucleus is no condition for maximum resonance. Throughout this paper, the data of the corresponding nitro compounds have been measured fo
ISSN:0165-0513
DOI:10.1002/recl.19530720303
出版商:WILEY‐VCH Verlag
年代:1953
数据来源: WILEY
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3. |
The Hofmann degradation of 4‐hydroxy‐phthalimide |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 72,
Issue 3,
1953,
Page 195-201
C. van der Stelt,
B. G. Suurmond,
W. Th. Nauta,
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摘要:
AbstractAccording toRodionowandFedorowa1), Hofmann degradation of 4‐hydroxy‐phthalimide yields 2‐amino‐4‐hydroxy‐benzoic acid. This has been shown to be incorrect. Only 2‐amino‐5‐hydroxy‐benzoic acid could be isolated from the reaction mixture. The spectra of both the acids mentioned were measured, and a few deriva
ISSN:0165-0513
DOI:10.1002/recl.19530720304
出版商:WILEY‐VCH Verlag
年代:1953
数据来源: WILEY
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4. |
The hydrolysis of methylene diurea |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 72,
Issue 3,
1953,
Page 202-206
J. I. de Jong,
J. de Jonge,
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摘要:
AbstractThe hydrolysis of methylene diurea giving urea and monomethylolurea was found to be a monomolecular reaction. The rate of the reaction is directly proportional to the hydrogen ion concentration in the pH range measured (3‐5) and independent of the buffer concentration. The activation energy appeared to be 19.5 kcal.Generally, the reaction of an amidomethylol group with an amide group leading to the formation of a methylene bridge between urea fragments, will be a reversible reaction. The rates of both the forward and the reverse reactions are proportional to the hydrogen ion concentratio
ISSN:0165-0513
DOI:10.1002/recl.19530720305
出版商:WILEY‐VCH Verlag
年代:1953
数据来源: WILEY
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5. |
Kinetics of the reaction between mono‐methylolurea and methylene diurea |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 72,
Issue 3,
1953,
Page 207-212
J. I. de Jong,
J. de Jonge,
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摘要:
AbstractThe reaction between monomethylolurea and methylene diurea appeared to be bimolecular and the rate constants were found to be directly proportional to the concentration of the hydrogen ions. An influence of the buffer concentration was not observed. The activation energy was found to be 15 kcal/mol.
ISSN:0165-0513
DOI:10.1002/recl.19530720306
出版商:WILEY‐VCH Verlag
年代:1953
数据来源: WILEY
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6. |
The reaction of methylene diurea with formaldehyde |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 72,
Issue 3,
1953,
Page 213-217
J. I. de Jong,
J. de Jonge,
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摘要:
AbstractThe reaction of methylene diurea with formaldehyde showed a close resemblance to the previously studied reaction of urea and formaldehyde1), i.e. the reaction appeared to be bimolecular and the rates were found to be directly proportional to the concentration of hydroxyl ions while further an influence of the buffer concentration on the rates was observed. Obviously the reaction is subject to a general acid and/or base catalysis. The activation energy appeared to be about 15 kcal/mol. The values for the rate constants were almost the same as were found for the reaction between urea and formaldehyde.
ISSN:0165-0513
DOI:10.1002/recl.19530720307
出版商:WILEY‐VCH Verlag
年代:1953
数据来源: WILEY
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7. |
Rayonne‐viscose ‐ role physico‐chimique des bains de regeneration |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 72,
Issue 3,
1953,
Page 218-226
Jean‐Charles Pariaud,
Jean Ferrier,
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摘要:
AbstractL'influence des concentrations des bains acides, sur le processus de régénération de la cellulose à partir de la viscose a été éxaminée. La méthode statique employée, en dehors de la filature, est basée sur la mesure de L'épaisseur de la couronne de cellulose, apparaissant lorsqu'on trempe un cylindre de viscose dans ces bains. On propose une interprétation
ISSN:0165-0513
DOI:10.1002/recl.19530720308
出版商:WILEY‐VCH Verlag
年代:1953
数据来源: WILEY
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8. |
Etude physico‐chimique de la vagotonine: I. Électrophorèse |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 72,
Issue 3,
1953,
Page 227-231
G. F. Michel,
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摘要:
AbstractL'hétérogénéité de la vagotonine a été signalée par quelques auteurs. Nous avons étudié le comportement de cette substance et des différentes fractions isolées par précipitation saline, à L'électrophorèse et à L'ult
ISSN:0165-0513
DOI:10.1002/recl.19530720309
出版商:WILEY‐VCH Verlag
年代:1953
数据来源: WILEY
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9. |
Etude physico‐chimique de la vagotonine: II. Ultracentrifugation |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 72,
Issue 3,
1953,
Page 232-235
G. F. Michel,
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摘要:
AbstractNos premiers essais de fractionnement de la vagotonine isolée du pancréas parSantenoise1) nous ont amenés à séparer par précipitation fractionnée au sulfate de lithium deux fractions de solubilités différentes2). Nous avons par la suite fractionné de nouveau la portion la plus soluble, et dans une précédente communication3), nous avons décrit leur comportement électrophorétique. Ces substances se sont révélées non homogènes à L'électrophorèse et renferment trois composés principaux accompagnés d'autres protéines en proportions plus faibles. Nous avons voulu vérifier si cette hétérogénéité se manifestait également lors de la sédi
ISSN:0165-0513
DOI:10.1002/recl.19530720310
出版商:WILEY‐VCH Verlag
年代:1953
数据来源: WILEY
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10. |
Chloramphenicol analogues I:DL‐2‐dichloroacetamido‐1‐(4‐pyridyl)‐1,3‐propanediol |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 72,
Issue 3,
1953,
Page 236-246
S. van der Meer,
H. Kofman,
H. Veldstra,
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摘要:
AbstractThe synthesis of one of the stereoisomeric forms (probably the threo‐form) ofDL‐2‐dichloroacetamido‐1‐(4‐pyridyl)‐1,3‐propanediol, the pyridine analogue of chloramphenicol, is described.Its activity againstSalm. typhimuriumandEbert. typhiis 1‐3 per cent of that of chl
ISSN:0165-0513
DOI:10.1002/recl.19530720311
出版商:WILEY‐VCH Verlag
年代:1953
数据来源: WILEY
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