1. |
Aromatic sulphonation V: A kinetic study on the sulphonation of toluene, ethylbenzene and isopropylbenzene in aqueous sulphuric acid |
|
Recueil des Travaux Chimiques des Pays‐Bas,
Volume 82,
Issue 2,
1963,
Page 113-120
A. W. Kaandorp,
H. Cerfontain,
F. L. J. Sixma,
Preview
|
PDF (367KB)
|
|
摘要:
AbstractRate measurements have been made on the homogeneous sulphonation of toluene in aqueous sulphuric acid varying from 70.0 to 95.9 wt‐% at 5.0°, 25.0° and 45.0°. In addition, rate constants have been determined for the homogeneous sulphonation of ethylbenzene and isopropylbenzene at 25.0° in aqueous sulphuric acid solutions varying from 72.4 to 89.1 wt‐%. All reactions were found to be first order with respect to the aromatic compound. It is suggested that the differences in the overall rate constants for the sulphonation of toluene, ethylbenzene and isopropylbenzene originate predominantly from steric hindrance forortho‐sub
ISSN:0165-0513
DOI:10.1002/recl.19630820202
出版商:WILEY‐VCH Verlag
年代:1963
数据来源: WILEY
|
2. |
Microbiological conversion of 19‐nortestosterone: (I) 16‐hydroxylation |
|
Recueil des Travaux Chimiques des Pays‐Bas,
Volume 82,
Issue 2,
1963,
Page 121-128
J. de Flines,
W. F. van der Waard,
W. J. Mijs,
S. A. Szpilfogel,
Preview
|
PDF (359KB)
|
|
摘要:
AbstractThe microbiological transformation of 19‐nortestosterone withMycosphaerella latebrosaand withHypomyces aurantius, leading to the 16β‐ and 16α‐hydroxy‐derivatives, respectively, is
ISSN:0165-0513
DOI:10.1002/recl.19630820203
出版商:WILEY‐VCH Verlag
年代:1963
数据来源: WILEY
|
3. |
Microbiological conversion of 19‐nortestosterone: (II)10‐ and 11‐hydroxylation |
|
Recueil des Travaux Chimiques des Pays‐Bas,
Volume 82,
Issue 2,
1963,
Page 129-138
J. de Flines,
W. F. van der Waard,
W. J. Mijs,
S. A. Szpilfogel,
Preview
|
PDF (467KB)
|
|
摘要:
AbstractFermentation of 19‐nortestosterone withCurvularia lunataor withBotrytis paeoniaeyielded mainly the 10β‐hydroxy‐derivative. Fermentation withAspergillus ochraceusafforded the 11α‐hydroxy‐derivative in good yield.10β‐Hydroxy‐19‐nortestosterone withCorynebacterium simplexyielded 10β, 17β‐dihydroxy‐19‐
ISSN:0165-0513
DOI:10.1002/recl.19630820204
出版商:WILEY‐VCH Verlag
年代:1963
数据来源: WILEY
|
4. |
Microbiological conversion of 19‐nortestosterone: (III)12‐hydroxylation |
|
Recueil des Travaux Chimiques des Pays‐Bas,
Volume 82,
Issue 2,
1963,
Page 139-142
J. de Flines,
W. F. van der Waard,
W. J. Mijs,
L. A. van Dijck,
S. A. Szpilfogel,
Preview
|
PDF (197KB)
|
|
摘要:
AbstractThe microbiological reaction of 19‐nortestosterone withColletotrichum derridisyielding mainly 12β‐hydroxy‐19‐nortestosterone, is d
ISSN:0165-0513
DOI:10.1002/recl.19630820205
出版商:WILEY‐VCH Verlag
年代:1963
数据来源: WILEY
|
5. |
Microbiological conversion of 19‐nortestosterone: (IV)15α‐hydroxylation |
|
Recueil des Travaux Chimiques des Pays‐Bas,
Volume 82,
Issue 2,
1963,
Page 143-148
J. de Flines,
W. F. van der Waard,
W. J. Mijs,
S. A. Szpilfogel,
Preview
|
PDF (266KB)
|
|
摘要:
AbstractMicrobiological reaction of 19‐nortestosterone withPenicilliumsp.ATCC 11598 leading to about equal amounts of the 15α‐hydroxy‐derivative and 15α‐hydroxy‐19‐nor‐androst‐4‐one‐3,17‐dione is described. Fermentation of 19‐nortestosterone withFusarium orthocerasafforded mainly 15α‐hydroxy‐19‐norandrost‐4‐ene‐3,17‐dione and only minor a
ISSN:0165-0513
DOI:10.1002/recl.19630820206
出版商:WILEY‐VCH Verlag
年代:1963
数据来源: WILEY
|
6. |
Microbiological conversion of 19‐nortestosterone: (V)6β‐ and 14α‐hydroxylation |
|
Recueil des Travaux Chimiques des Pays‐Bas,
Volume 82,
Issue 2,
1963,
Page 149-156
J. de Flines,
W. F. van der Waard,
W. J. Mijs,
L. A. van Dijck,
S. A. Szpilfogel,
Preview
|
PDF (351KB)
|
|
摘要:
AbstractThe microbiological reactions of 19‐nortestosterone withHelminthosporium kusanoileading to the 6β‐hydroxy‐derivative and withHelminthosporium buchloesleading to the 14α‐hydroxy‐derivative ar
ISSN:0165-0513
DOI:10.1002/recl.19630820207
出版商:WILEY‐VCH Verlag
年代:1963
数据来源: WILEY
|
7. |
Chemistry of acetylenic ethers 63: The synthesis of α,β‐unsaturated thiolesters from carbonyl compounds, acetylenic thioethers, and boron trifluoride |
|
Recueil des Travaux Chimiques des Pays‐Bas,
Volume 82,
Issue 2,
1963,
Page 157-171
L. B. Bos,
J. F. Arens,
Preview
|
PDF (651KB)
|
|
摘要:
AbstractThe α,β‐unsaturated thiolesters listed in Table I have been prepared by treating a mixture of a carbonyl compound and boron trifluoride with an acetylenic thioether (see reaction scheme 2). Good yields are obtained when ethers are used as solvents. The configuration of the esters prepared from aldehydes istrans. From unsymmetrical ketones mixtures ofcisandtransisomers are for
ISSN:0165-0513
DOI:10.1002/recl.19630820208
出版商:WILEY‐VCH Verlag
年代:1963
数据来源: WILEY
|
8. |
Thermal substitution reactions of cupric benzoate II |
|
Recueil des Travaux Chimiques des Pays‐Bas,
Volume 82,
Issue 2,
1963,
Page 172-176
W. Schoo,
J. U. Veenland,
Th. J. de Boer Boer,
F. L. J. Sixma,
Preview
|
PDF (156KB)
|
|
摘要:
AbstractAfter thermal decomposition of cupric benzoate in the presence of deuterium oxide 43% ofortho‐deutero‐benzoic acid can be obtained beside phenol. A radical mechanism for the air oxidation of benzoic acid to phenol under the catalytic influence of copper oxide should therefore be reasona
ISSN:0165-0513
DOI:10.1002/recl.19630820209
出版商:WILEY‐VCH Verlag
年代:1963
数据来源: WILEY
|
9. |
The condensation of rhodanine and derivatives with aromatic aldehydes containing iodine |
|
Recueil des Travaux Chimiques des Pays‐Bas,
Volume 82,
Issue 2,
1963,
Page 177-182
F. J. Allan,
G. G. Allan,
Preview
|
PDF (262KB)
|
|
ISSN:0165-0513
DOI:10.1002/recl.19630820210
出版商:WILEY‐VCH Verlag
年代:1963
数据来源: WILEY
|
10. |
Chemistry of acetylenic ethers, 64: Some remarks concerning the “nucleophilic substitution at an acetylenic carbon” |
|
Recueil des Travaux Chimiques des Pays‐Bas,
Volume 82,
Issue 2,
1963,
Page 183-188
J. F. Arens,
Preview
|
PDF (270KB)
|
|
摘要:
AbstractThe suggestion is put forward that nucleophilic displacements of a group X in compounds RC CX may occur through substitution at X rather than at the acetylenic carbon atom bearing
ISSN:0165-0513
DOI:10.1002/recl.19630820211
出版商:WILEY‐VCH Verlag
年代:1963
数据来源: WILEY
|