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1. |
2‐deuteromethylation of ketones |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 12,
Issue 1,
1976,
Page 1-6
Benzion Fuchs,
Mordechai Pasternak,
Sarah Weinman,
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摘要:
AbstractA methods of obtaining 2‐deuteromethyl ketones by deuteromethylation of the corresponding β‐ketosters. is described and proposed as a general method for β‐deuterium labeling of
ISSN:0362-4803
DOI:10.1002/jlcr.2580120102
出版商:John Wiley&Sons, Ltd.
年代:1976
数据来源: WILEY
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2. |
Synthesis of14C‐labelled 4‐hydroperoxyisophosphamide, an effective antitumor agent |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 12,
Issue 1,
1976,
Page 7-11
T. Nagasaki,
Y. Katsuyama,
H. Minato,
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摘要:
Abstract4‐Hydroperoxyisophosphamide (II), an effective antitumor agent has been labelled with carbon‐14. The carbon‐14 label was incorporated into the C‐6 position of the molecule to give (VII). The overall radiochemical yield was 4.4% based on barium carbonate‐14C. The labelled compound obtained was used for absorption and metabolis
ISSN:0362-4803
DOI:10.1002/jlcr.2580120103
出版商:John Wiley&Sons, Ltd.
年代:1976
数据来源: WILEY
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3. |
Synthesis of deuterium and tritium labelled derivatives of maleopimaric acid |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 12,
Issue 1,
1976,
Page 13-22
Peter J. Ramm,
John B. Taylor,
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摘要:
AbstractA new hepatoprotective agent, N‐(2‐hydroxyethyl)‐maleopimarimidyl morpholide (RU18492) has been synthesised labelled with tritium at C‐3, C‐4a, C‐10 and in the C‐isopropyl group. The incorporation of tritium relies on the acid‐catalysed isomerisation of levopimaric acid (4) to abietic acid (2), which was then converted in thre
ISSN:0362-4803
DOI:10.1002/jlcr.2580120104
出版商:John Wiley&Sons, Ltd.
年代:1976
数据来源: WILEY
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4. |
Synthesis of14C‐desmethylene aldrin, desmethylene dieldrin and desmethylene aldrincisandtrans‐dihydrddiols |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 12,
Issue 1,
1976,
Page 23-30
Michael P. Walker,
James D. McKinney,
Vamanmurti G. Mudgal,
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摘要:
AbstractThe synthesis of14C‐desmethylene aldrin (I) from14C‐Ul‐hexachloro cyclopentadiene and cyclohexa‐l,4‐dieneviaa Diels‐Alder reaction and its conversion to desmethylene dieldrin (II) and desmethylenecis(III) andtrans(IV)‐dihydrodiols
ISSN:0362-4803
DOI:10.1002/jlcr.2580120105
出版商:John Wiley&Sons, Ltd.
年代:1976
数据来源: WILEY
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5. |
Synthese asymetrique de la D(+) amphetamine‐14C‐7 par l'intermediaire du benzyl‐2 methyl‐2 dithianne‐l,3 |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 12,
Issue 1,
1976,
Page 31-39
L. Pichat,
J‐P. Beaucourt,
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摘要:
AbstractBenzyl chloride‐7‐14C is condensed with 2‐lithio 2‐methyl 1,3‐dithianes. Deprotection with cupric chloride‐copper oxide of the resulting 2‐benzyl 2‐methyl 1,3‐dithianes leads to 1‐phenyl‐2‐propanone‐1‐14C. The latter with L(‐)α‐methylbenzylamine in presence of molecuLar sieve gives rise to (‐)N‐(α‐phen‐ethyl)phenylisopropylimine which is catalytically reduced into the corresponding amine. Hydrogenolysis of this amine gives D(+) amphetamine‐7‐14C isolated as the sulfate with an overall yield of 10 % based on be
ISSN:0362-4803
DOI:10.1002/jlcr.2580120106
出版商:John Wiley&Sons, Ltd.
年代:1976
数据来源: WILEY
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6. |
Synthesis of14c‐labeled 2,2‐dichloropropionic acid |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 12,
Issue 1,
1976,
Page 41-51
F. S. Tanaka,
R. G. Wien,
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摘要:
AbstractA widely used herbicide, 2,2‐dichloropropionic acid (dalapon), was synthesized with14C‐labeling in the C‐1 or C‐2 positions. The carboxyl labeled material was prepared in 55% yield by carbonation of 1,1‐dichloro‐ethyllithium at approximately −104°. Starting with trichloroacetic acid, the C‐2 labeled product was prepared in an overall yield of 39% by means of a 4‐step reaction sequence which involved the removal of a chlorine atom and the addition
ISSN:0362-4803
DOI:10.1002/jlcr.2580120107
出版商:John Wiley&Sons, Ltd.
年代:1976
数据来源: WILEY
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7. |
A quantitative stereoselective synthesis of radiolabelled PGF2αfrom arachidonate or PGE2 |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 12,
Issue 1,
1976,
Page 53-62
K. J. Stone,
M. Hart,
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摘要:
AbstractA simple, efficient and relatively cheap procedure for synthesising radiolabelled PGF2αfrom arachidonate or PGE2is described. The method exploits the stereospecific enzymatic reduction of PGE2by PGE2‐9‐ketoreductase from rabbit renal co
ISSN:0362-4803
DOI:10.1002/jlcr.2580120108
出版商:John Wiley&Sons, Ltd.
年代:1976
数据来源: WILEY
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8. |
The synthesis of18O multilabeled anhydrous nitric acid |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 12,
Issue 1,
1976,
Page 63-67
A. C. Scott,
J. H. McReynolds,
M. Anbar,
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摘要:
Abstract18O‐multilabeled anhydrous nitric acid (89 atom %18O) was prepared by exchange with H218O, neutralization with NH3, and distillation from methane sulfonic acid. The use of trifluoromethane sulfonic acid, sulfuric acid, and oleum was also investigated, but these acids were found unsuitable due to rapid oxygen exchange. The extent of exchange was. monitored by converting water to methanol, nitric acid to nitroanisole, and analyzing by field ionization mass spectrometr
ISSN:0362-4803
DOI:10.1002/jlcr.2580120109
出版商:John Wiley&Sons, Ltd.
年代:1976
数据来源: WILEY
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9. |
Synthesis of deuterium‐labelled drugs of abuse for use as internal standards in quantification by selected ion monitoring. I. Methamphetamine; 2,5‐dimethoxy‐4‐methylamphetamine (DOM); phencyclidine (PCP); and methaqualone |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 12,
Issue 1,
1976,
Page 69-78
Allison F. Fentimanjr,
Rodger L. Foltz,
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摘要:
AbstractFour deuterium‐labelled compounds were prepared for use as internal standards in the quantification of methamphetamine, DOM, PCP, and methaqualone at low levels in body fluids by selected ion monitoring. The need for standards containing more than three deuterium atoms per molecule and having high isotopic purity is discusse
ISSN:0362-4803
DOI:10.1002/jlcr.2580120110
出版商:John Wiley&Sons, Ltd.
年代:1976
数据来源: WILEY
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10. |
Synthese von Pulvinsäure‐[14C], 4‐Hydroxy‐Pulvinsäure‐[14C] und 4′‐Hydroxy‐Pulvinsäure‐[14C] |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 12,
Issue 1,
1976,
Page 79-96
Hans Ehrenfried Noppel,
Karl‐Heinz Schweer,
Friedrich Von Massow,
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摘要:
AbstractEs wird die Synthese von Pulvinäure‐[14C], 4′‐Hydroxy‐pulvinäure‐[14C], ausgehend von Phenylacetonitril‐[2‐14C], bschrieben. Die Identität der markierten Verbindungen wurde durch dünnschichtchtomatographischen Vergleich mit den auf glechim Wege synthetisierten inaktiven substanzen sichergestellt, deren Struktur durch Elementaranalyse, MASSEN‐,1H‐NMR‐Spektern
ISSN:0362-4803
DOI:10.1002/jlcr.2580120111
出版商:John Wiley&Sons, Ltd.
年代:1976
数据来源: WILEY
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