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1. |
An improved synthesis of labelled dibromochloropropane |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 18,
Issue 12,
1981,
Page 1713-1719
O. Buchman,
J. Azran,
I. Pri‐Bar,
M. Shimoni,
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摘要:
AbstractA continuous three‐step micro‐synthesis of 1,2‐dibromo‐3‐chloropropane, labelled with tritium in position 1 and 2, is described. A specific activity of 10.8 Ci/mmol is obtained. The yield observed in the uninterrupted overall synthesis is appreciably lower than that in the controlled step‐by‐s
ISSN:0362-4803
DOI:10.1002/jlcr.2580181202
出版商:John Wiley&Sons, Ltd.
年代:1981
数据来源: WILEY
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2. |
Labelling of fluorinated aromatics by isotopic exchange with [18F]fluoride |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 18,
Issue 12,
1981,
Page 1721-1730
Fulvio Cacace,
Maurizio Speranza,
Alfred P. Wolf,
Joanna S. Fowler,
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摘要:
AbstractThe efficient and rapid nucleophilic exchange of fluorine by fluoride‐18F ion in aromatic rings is reported here utilizing rubidium‐18F‐fluoride in DMSO on model compounds. Specific activities in the 3 × 104Ci/mol region are readily achievable. Nucleophilic substitution is shown to be an attractive modality for fluorine‐18 labeling of aromatic c
ISSN:0362-4803
DOI:10.1002/jlcr.2580181203
出版商:John Wiley&Sons, Ltd.
年代:1981
数据来源: WILEY
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3. |
Synthesis of14C‐labelled 1‐(4‐chlorobenzyl)‐3‐methyl‐3‐(2‐hydroxyethyl)‐thiourea |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 18,
Issue 12,
1981,
Page 1731-1735
K. Esses‐Reiter,
J. Reiter,
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摘要:
Abstract1‐(4‐Chlorobenzyl)‐3‐methyl‐3‐(2‐hydroxyethyl)‐thiourea labelled with14C at its urea group was synthesised starting from potassium cyanide‐14C, via potassium thiocyanate‐14C, 4‐chlorobenzyl‐thiocyanate‐14C and 4‐chlorobenzyl‐isothiocyanate‐14C. The conditions of the isomerisation of 4‐chlorobenzyl‐thiocyanate‐14C to 4‐chlorobenzyl‐
ISSN:0362-4803
DOI:10.1002/jlcr.2580181204
出版商:John Wiley&Sons, Ltd.
年代:1981
数据来源: WILEY
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4. |
Synthesis of tritium labelled precocenes |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 18,
Issue 12,
1981,
Page 1737-1741
A. Banerji,
N. C. Goomer,
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摘要:
AbstractRegiospecific syntheses of tritium labelled precocene I (5a) and precocene II (5b), the antijuvenile hormones, have been accomplished. The syntheses involved condensations between 2‐hydroxyacetophenones (1) with acetone‐T to give cross condensation products2which on cyclodehydration furnished 2,2‐dimethyl‐4‐chromanones‐(2‐gem dimethyl‐T) (3). Reduction of3with lithium aluminium hydride gave chroman‐4‐ols (2‐gem dimethyl‐T) (4). Dehydration of4furnished 2,2‐dimethyl‐ chromenes‐ (2‐gem dimethyl‐T) (5). Starting with appropriate acetophenones and acetone‐T, precocene I (7‐methoxy‐2,2‐dimethylchromene) and precocene II (6, 7‐dimethoxy‐2, 2‐dimethylchromene) labelled with tritium in the 2‐gemdimethylpositions, have been synthesised
ISSN:0362-4803
DOI:10.1002/jlcr.2580181205
出版商:John Wiley&Sons, Ltd.
年代:1981
数据来源: WILEY
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5. |
The use of the acetonide derivative in the preparation of D‐threo‐chloramphenicol‐1‐3H and its nitroso derivative |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 18,
Issue 12,
1981,
Page 1743-1753
J. Richard Heys,
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摘要:
AbstractAn efficient synthesis of millimolar quantities of high specific activity D‐threo‐chloramphenicol‐1‐3H is described. The key step is the chromatographic separation of the compound from its 1‐epimer, produced in the Ca(B3H4)2reduction of chloramphenicol ketone (D‐α‐dichloroacetyl‐amino‐β‐hydroxy‐p‐nitropropiophenone), by use of the acetonide derivative. Stereochemical aspects of the N‐bromosuccinimide oxidation of chloramphenicol to chloramphenicol ketone have been investigated, and the previously reported [1] specific rotation of chloramphenicol ketone has been corrected. The synthesis of nitrosochlora
ISSN:0362-4803
DOI:10.1002/jlcr.2580181206
出版商:John Wiley&Sons, Ltd.
年代:1981
数据来源: WILEY
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6. |
Small‐scale preparation of14C2‐pentaerythritol |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 18,
Issue 12,
1981,
Page 1755-1758
Alexander B. Susàn,
William P. Duncan,
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摘要:
Abstract14C2‐Pentaerythritol (14C‐PE) at approximately 8 mCi/mmole was prepared in 76% yield on a 3‐mmole scale via a base‐catalyzed condensation of acetaldehyde‐14C2with 1.5% aqu
ISSN:0362-4803
DOI:10.1002/jlcr.2580181207
出版商:John Wiley&Sons, Ltd.
年代:1981
数据来源: WILEY
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7. |
Synthesis of14C‐labeled 4‐acetyl‐5,6‐bis(4‐chlorophenyl)‐2‐(2‐hydroxyethyl)‐2H‐pyridazin‐3‐one |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 18,
Issue 12,
1981,
Page 1759-1763
Russell Buchman,
T. R. Evans,
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摘要:
AbstractA simple and convenient synthesis of a radiolabeled antihypertensive pyridazinone was developed. The product was purified chromatographically, and the chemical and radiochemical purities of the sample were determined.
ISSN:0362-4803
DOI:10.1002/jlcr.2580181208
出版商:John Wiley&Sons, Ltd.
年代:1981
数据来源: WILEY
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8. |
Synthesis of carbon‐14‐labelled antibacterial agent. Synthesis of 1‐ethyl‐ [1‐14C]‐6‐fluoro‐1, 4‐dihydro‐4‐oxo‐7‐ (1‐piperazinyl)‐3‐quinolinecarboxylic acid (14C‐AM‐715) |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 18,
Issue 12,
1981,
Page 1765-1771
Y. Nagatsu,
T. Irikura,
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摘要:
Abstract1‐Ethyl‐6‐fluoro‐1,4‐dihydro‐4‐oxo‐7‐(1‐piperazinyl)‐ 3‐quinolinecarboxylic acid (I, AM‐715), a new potent antibacterial agent, was labelled with carbon‐14 at the C‐1 position of the N‐ethyl group for metabolic studies. The synthesis was achieved according to two reaction routes. The overall radiochemical yields of14C‐AM‐715 based on ethyl iodide‐1‐14C from route A and rou
ISSN:0362-4803
DOI:10.1002/jlcr.2580181209
出版商:John Wiley&Sons, Ltd.
年代:1981
数据来源: WILEY
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9. |
Synthesis of methionines specifically labelled with2H or13C |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 18,
Issue 12,
1981,
Page 1773-1784
David C. Billington,
Bernard T. Golding,
Michael J. Kebbell,
Ishaq K. Nassereddin,
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摘要:
AbstractEfficient methods for synthesising L‐[methy‐13C]methionine from [13C]iodomethane and L‐methionine, and L‐[3,4‐13C2] methionine from [13C2]ethene, are described; the preparation of [3,3‐2H2]methionine and [2,3,3‐2H3]methionine from methionine by an exchange metho
ISSN:0362-4803
DOI:10.1002/jlcr.2580181210
出版商:John Wiley&Sons, Ltd.
年代:1981
数据来源: WILEY
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10. |
A simple, one‐step synthesis of 1‐14C‐acetylhydrazine |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 18,
Issue 12,
1981,
Page 1785-1791
P. Mathiaparanam,
L. T. Wong,
B. H. Thomas,
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摘要:
AbstractA synthesis of 1‐14C‐acetylhydrazine by acetylation of hydrazine using 1‐14C‐ethyl acetate and a catalytic amount of activated alumina is de
ISSN:0362-4803
DOI:10.1002/jlcr.2580181211
出版商:John Wiley&Sons, Ltd.
年代:1981
数据来源: WILEY
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