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1. |
Synthesis of 1‐decene‐2‐13C |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 21,
Issue 9,
1984,
Page 793-797
Alan P. Marchand,
Riza Kaya,
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摘要:
AbstractA four‐step synthesis of 1‐decene‐2‐13C starting with 1‐bronooctane (57% overall yield) is
ISSN:0362-4803
DOI:10.1002/jlcr.2580210902
出版商:John Wiley&Sons, Ltd.
年代:1984
数据来源: WILEY
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2. |
The synthesis of α‐methylstyrenes with14C‐labelling in the side chain |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 21,
Issue 9,
1984,
Page 799-802
H. M. Ali,
C. A. Barson,
P. L. Coe,
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摘要:
Abstractα‐Methylstyrenes with all three side chain carbons specifically14C‐labelled have been synthesised by Wittig reactions between the appropriately labelled acetophenones or methylene triphenylphosphoranes. The yields in all cases were good and any radiochemical impurities could be readily removed by distilla
ISSN:0362-4803
DOI:10.1002/jlcr.2580210903
出版商:John Wiley&Sons, Ltd.
年代:1984
数据来源: WILEY
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3. |
Synthesis of hydroxyl[13N]amine and binding of13NH2OH to two transaminases |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 21,
Issue 9,
1984,
Page 803-814
Deborah S. Kaseman,
Arthur J. L. Cooper,
Alton Meister,
Alan S. Gelbard,
Robert E. Reiman,
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摘要:
AbstractNH2OH was labeled with a β+emitter (13N, t1/2= 9 96 min.). Hydroxyl[13N]amine was synthesized from HSO 3−and [13N]nitrite (produced via the160(p,α)13N reaction by proton bombardment of H2O). The synthesis reactions are:Hydroxyl[13N]amine was purified by ion‐exchange chromatography on Dowex‐1 × 8 (AcO−) to remove unreacted13NO 2−and13NO 3−. Radiochemical yields of 50–90% were obtained in 25–30 min. The purity and specific activity of13NH2OH were determined by HPLC analysis and spectrophotometric assay. The binding of13NH2OH to pig heart glutamate‐pyruvate transaminase and to pig heart glutamate‐oxaloacetate transaminase was measured. This work demonstrates that quantitation of the binding of hydroxylamine (an active‐site directed enzyme inhibitor) labeled with a positron‐emitting
ISSN:0362-4803
DOI:10.1002/jlcr.2580210904
出版商:John Wiley&Sons, Ltd.
年代:1984
数据来源: WILEY
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4. |
Synthesis of11C‐labelled choline |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 21,
Issue 9,
1984,
Page 815-820
Mirko Diksic,
Y. Lucas Yamamoto,
William Feindel,
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摘要:
AbstractWe report the synthesis of11C‐labelled choline using the reaction of “nocarrier‐added”11C‐labelled methyliodide and 2‐amino‐(N,N‐dimethyl)‐ethanol. After determining the optimum temperature and duration for the reaction, we achieved a radiochemical yield of about 30% and the radioactivity levels needed for PET
ISSN:0362-4803
DOI:10.1002/jlcr.2580210905
出版商:John Wiley&Sons, Ltd.
年代:1984
数据来源: WILEY
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5. |
Preparation of [131I] iodinated nonoxynol‐9 |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 21,
Issue 9,
1984,
Page 821-831
Bushra J. Agha,
George A. Garbolas,
Kathleen Wets,
George A. Digenis,
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摘要:
AbstractA novel method for the radioiodination [131I] of the multicomponent non‐ionic surfactant nonoxynol‐9 (N‐9) is described. The extent of incorporation and distribution of the131I‐label into the aromatic moiety of various ethoxymer units of N‐9 was determined utilizing a high pressure liquid chromatographic (HPL
ISSN:0362-4803
DOI:10.1002/jlcr.2580210906
出版商:John Wiley&Sons, Ltd.
年代:1984
数据来源: WILEY
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6. |
Synthesis of deuterium‐labeled 1‐aminocyclopropane‐1‐carboxylic acid |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 21,
Issue 9,
1984,
Page 833-841
Kondareddiar Ramalingam,
Douglas Kalvin,
Ronald W. Woodard,
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摘要:
AbstractThe syntheses of D,L‐1‐amino[2,2‐2H2]cyclopropane‐1‐carboxylic acid; 1‐amino [c‐2,c‐3‐2H2] and 1‐amino[t‐2,t‐3‐2H2]cyclopropane‐1‐carboxylic acid (cis‐[2H2]ACC); 1‐amino[2S,3S‐2H2] and 1‐amino[2R,3R‐2H2]cyclopropane‐1‐carboxylic acid (trans‐[2H2]ACC); and 1‐amino[2,2,3,3‐2H4]cyclopropane‐1‐carboxylic acid are described. The [2,2‐2H2]and [2,2,3,3‐2H4]ACC compounds were prepared from the appropriately deuterated 2‐bromoethanol 4‐methylbenzenesulfonates by reaction with ethyl isocyanoacetate and two moles of sodium hydride. Thetrans‐[2H2]ACC andcis[2H2]ACC were prepared frommesoandd, l‐[1,2‐2H2]‐1,2‐dibromoethane respectively, by reaction with ethyl isocyanoacetate and two moles of sodium hydride. These compounds are required for use in the study of the biosynthesis of ethylene by various plants and for use in1H
ISSN:0362-4803
DOI:10.1002/jlcr.2580210907
出版商:John Wiley&Sons, Ltd.
年代:1984
数据来源: WILEY
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7. |
Fast low temperature ultrasonic synthesis and injection ready preparation of carrier free 17‐I‐123‐heptadecanoic acid |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 21,
Issue 9,
1984,
Page 843-856
John Mertens,
Wim Vanryckeghem,
Axel Bossuyt,
Pierre Van Den Winkel,
René Vandendriessche,
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摘要:
Abstract17‐I‐123‐heptadecanoic acid is prepared carrier‐free from 17‐Br‐heptadecanoic acid in methyl ethyl ketone at 100°C. A quantitative labeling yield is obtained within 20 minutes using a 50 KHz ultrasonic bath. Sonication allows the presence of water up to 7.5% v/v. The pattern shown by the plot of the kinetic curves is typical of two consecutive reactions: the first being the dissociation of a radioactive side product, the second a I−for Br nucleophilic exchange. The pure carrier‐free radioiodinated fatty acid is obtained by HPLC separation and is used clinically in a sterile 6% human serum albumine solution. The quality control of the injection ready solution is based on the use of a RP18 S
ISSN:0362-4803
DOI:10.1002/jlcr.2580210908
出版商:John Wiley&Sons, Ltd.
年代:1984
数据来源: WILEY
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8. |
Reduction of iminium ethers with sodium boro[3H] hydride. Preparation of tritium labelled clomiphene and nitromiphene (CI 628) |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 21,
Issue 9,
1984,
Page 857-863
Peter C. Ruenitz,
Jerome R. Bagley,
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摘要:
AbstractThe preparation of [3H]‐clomiphene and [3H]‐nitromiphene from amido precursors in a two‐step reaction sequence utilizing NaB H4is described. The radiochemical yield and specific activity of the former are 34% and 16 mCi/mmol and those of the latter were 42% and 20 mCi/mmol, respectively. The method described is of micromolar scale designed for maintaining cost economy in the purchase of expensive radiolabelled reagents while yielding final products of sufficient radioactivity forin vitroandin vivometabolism st
ISSN:0362-4803
DOI:10.1002/jlcr.2580210909
出版商:John Wiley&Sons, Ltd.
年代:1984
数据来源: WILEY
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9. |
Syntheses of 5′‐deoxy‐5‐[18F] fluorouridine and related compounds as probes for measuring tissue proliferationin vivo |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 21,
Issue 9,
1984,
Page 865-873
Chyng‐Yann Shiue,
Alfred P. Wolf,
Morris Friedkin,
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摘要:
AbstractA rapid synthesis of 5′‐deoxy‐5‐[18F] fluorouridine (3a) from either [18F] F2or CH3CO218F is described. Fluorination of 2′,3′‐di‐O‐acetyl‐5′‐deoxyuridine (1a) with either [18F] F2or CH3CO218F in glacial acetic acid at room temperature followed by hydrolysis with sodium methoxide in methanol gives 5′‐deoxy‐5‐[18F] fluorouridine (3a) in radiochemical yields of 20‐25% in a synthesis time of 80 min from EOB. The same method also has been used to synthesize 5‐[18F] fluorouridine (3b) and 2′‐deoxy‐5‐[18F] fluorouridine (3c) in similar radiochemical yields. Acetyl hypofluorite (CH3CO2F) is prop
ISSN:0362-4803
DOI:10.1002/jlcr.2580210910
出版商:John Wiley&Sons, Ltd.
年代:1984
数据来源: WILEY
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10. |
Radiosynthesis of no‐carrier‐added75,77Br‐brombenperidol |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 21,
Issue 9,
1984,
Page 875-887
S. M. Moerlein,
G. Stöcklin,
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摘要:
AbstractA three‐step synthesis of the neuroleptic benperidol is presented, and the rapid no‐carrier‐added (n.c.a.) radiobromination of this compound to form brombenperidol (BBP), a radiolabelled dopaminergic receptor‐binding ligand, is described. N.c.a. radiobromination of benperidol using dichloramine‐T in trifluoroacetic acid at elevated temperatures results in bromination totally at the benzimidazolinyl ring of the neuroleptic, leaving the molecular characteristics necessary for receptor binding unaltered. Radiopharmaceutical production results in n.c.a.75,77Br‐brombenperidol with a corrected radiochemical yield of 30% and a specific activity exceeding 8,
ISSN:0362-4803
DOI:10.1002/jlcr.2580210911
出版商:John Wiley&Sons, Ltd.
年代:1984
数据来源: WILEY
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