1. |
The dielectric properties of some simple triglycerides |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 90,
Issue 10,
1971,
Page 1055-1068
A.M. Ras,
P. Bordewijk,
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摘要:
AbstractValues of ϵ′ and ϵ″ were determined for glycerol triacetate, tripropionate, and tributyrate in the frequency ranges 120 Hz to 100 kHz and 100 MHz to 9 GHz. The temperature‐dependence of the static dielectric constant indicates that the conformation of the molecules changes with the temperature. This conclusion is corroborated by the fact that for the triacetate and the tripropionate the distribution of relaxation times becomes broader with increasing temp
ISSN:0165-0513
DOI:10.1002/recl.19710901002
出版商:WILEY‐VCH Verlag
年代:1971
数据来源: WILEY
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2. |
Unconventional nucleotide analogues. VI.Synthesis of Purinyl‐ and Pyrimidinyl‐Peptides |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 90,
Issue 10,
1971,
Page 1069-1080
H. de Koning,
U.K. Pandit,
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摘要:
AbstractHomogeneous and heterogeneous peptides have been synthesized from pyrimidinyl‐ and purinyl‐amino acids la, b, c. Investigation of the oligopeptide derived from 1a (poly‐1a) showed no secondary structure as a result of base‐base interaction: however, the polymer was found to complex weakly with poly‐adenylic acid. Poly‐1a also exhibited a stimulation of phenylalanine incorporation in thein vitrosynthesis of poly‐
ISSN:0165-0513
DOI:10.1002/recl.19710901003
出版商:WILEY‐VCH Verlag
年代:1971
数据来源: WILEY
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3. |
The nitration of mono‐alkylbenzenes conformational analysis and steric hindrance: Part I:Primaryalkylbenzenes |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 90,
Issue 10,
1971,
Page 1081-1088
J.M.A. Baas,
B.M. Wepster,
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摘要:
AbstractThe partial rate factors for the nitration of sevenprimaryalkylbenzenes have been determined. The activation entropy of theortho‐substitution in neopentylbenzene is 2.9±1.7 e.u. smaller than that of thepara‐substitution. The steric hindrance of the nitration in theortho‐positions has been discussed by reference to the conformations of the initial states and the transition states. The increase of the steric hindrance is compensated by the increase of the polarizability of the alkyl
ISSN:0165-0513
DOI:10.1002/recl.19710901004
出版商:WILEY‐VCH Verlag
年代:1971
数据来源: WILEY
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4. |
The nitration of mono‐alkylbenzenes conformational analysis and steric hindrance: Part II:Secondaryalkylbenzenes |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 90,
Issue 10,
1971,
Page 1089-1097
J.M.A. Baas,
B.M. Wepster,
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摘要:
AbstractThe isomer distributions for the nitration of sixsecondaryalkylbenzenes and the partial rate factors of three of these compounds have been determined. The steric hindrance of the nitration in theortho‐position of isopropylbenzene is mainly of an enthalpic nature. The increase of this hindrance in the series of isopropylbenzene,s‐butylbenzene, (1‐ethylpropyl)benzene is of an entropic nature and can be explained from the conformational analysis of the initial states and the transition states. The steric hindrance in theortho‐positions of (2‐methyl‐1‐ isopropylpropyl)benzene and (1‐t‐butyl‐2.2‐dimethylpropyl)
ISSN:0165-0513
DOI:10.1002/recl.19710901005
出版商:WILEY‐VCH Verlag
年代:1971
数据来源: WILEY
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5. |
1‐alkynyl thiocyanates andN,N‐dialkyl‐1‐alkynesulfenamides: (Short Communication) |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 90,
Issue 10,
1971,
Page 1098-1100
J. Meijer,
L. Brandsma,
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ISSN:0165-0513
DOI:10.1002/recl.19710901006
出版商:WILEY‐VCH Verlag
年代:1971
数据来源: WILEY
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6. |
Cobalticenium salts. I: Reaction of cobaltocene with hydrogen halides and with triphenylphosphonium halides |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 90,
Issue 10,
1971,
Page 1101-1109
M. van Den Akker,
F. Jellinek,
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摘要:
AbstractReaction of cobaltocene with hydrogen halides HX (X = Cl, Br, I) in ethereal solution yields the ionic complexes [Cp2Co]+2[CoX4]2−in high yields. If triphenylphosphine is present in the reaction mixtures, the cobalticenium halides [Cp2Co]X are formed as the main products. Reaction of cobaltocene with hydrogen fluoride gives [Cp2Co][HF2]. The mechanisms of these reactions are discusse
ISSN:0165-0513
DOI:10.1002/recl.19710901007
出版商:WILEY‐VCH Verlag
年代:1971
数据来源: WILEY
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7. |
Chemistry of cyclopropene preparation and reactivity of the cycloprop‐1‐enyl anion in liquid ammonia: (Preliminary communication) |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 90,
Issue 10,
1971,
Page 1110-1112
A.J. Schipperijn,
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摘要:
AbstractIt has long been recognized that the vinylic hydrogens of cyclopropene have an acidity comparable to that of the hydrogens of acetylene1, but it is only in isolated cases that this property has been turned to advantage in the synthesis of substituted cyclopropene derivatives2‐7. In this communication we report the preparation of the cycloprop‐1‐enyl anion and its reaction with cyclopropene and alkyl h
ISSN:0165-0513
DOI:10.1002/recl.19710901008
出版商:WILEY‐VCH Verlag
年代:1971
数据来源: WILEY
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8. |
Simplified synthetic routes to symmetrical heterohelicenes |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 90,
Issue 10,
1971,
Page 1113-1118
P.G. Lehman,
Hans Wynberg,
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摘要:
AbstractThe synthetic route to heterohelicenes has been simplified significantly by a judicious choice of starting materials and the use of appropriate intermediates.
ISSN:0165-0513
DOI:10.1002/recl.19710901009
出版商:WILEY‐VCH Verlag
年代:1971
数据来源: WILEY
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9. |
Vapour phase thermolysis of allyl phenyl ether |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 90,
Issue 10,
1971,
Page 1119-1122
R. Louw,
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ISSN:0165-0513
DOI:10.1002/recl.19710901010
出版商:WILEY‐VCH Verlag
年代:1971
数据来源: WILEY
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10. |
Vinyl orthoformates and vinyl acetals. Part I: Synthesis of divinyloxymethyl and diaryloxymethyl halides and carboxylates |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 90,
Issue 10,
1971,
Page 1123-1128
J.W. Scheeren,
J.E.W. van Melick,
R.J.F. Nivard,
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摘要:
AbstractDiaryloxymethyl halides and divinyloxymethyl halides, formates, trichloro‐acetates, monochloroacetates, and acetates have been synthesized from corresponding vinyl orthoformate
ISSN:0165-0513
DOI:10.1002/recl.19710901011
出版商:WILEY‐VCH Verlag
年代:1971
数据来源: WILEY
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