Journal of Labelled Compounds

Titel Veröffentlichungsdatum Sprache Zitate
Synthesis of carbon‐14 labeled diphenylhydantoin and its major metabolite 5‐(p‐hydroxyphenyl)‐5‐phenylhydantoin (HPPH) in 70 minutes1974/07/01English4
A convenient procedure for the biosynthesis and isolation of 35S‐adenosylmethionine1966/01/01English4
Synthesis of 14C‐labelled (+)‐limonene1974/04/01English4
Radiosynthesen biologisch aktiver verbindungen. II Triforine (cela W 524) markiert mit tritum und 14C1973/01/01English4
The synthesis of p32 labelled polyalkyl polyphosphonates (phosphonated polyethylene)1971/07/01English4
New possibilities of enzymic synthesis of radioactive nucleotides. I. Synthesis of radioactive nucleoside‐5′‐triphosphates by an enzyme of Escherichia coli B1969/10/01English4
Preparation of [2‐14C]‐2‐(p‐chlorophenoxy)‐2‐methylpropionic acid and its ethyl ester, [14C] clofibrate1975/01/01English4
A gas‐chromatographic method for the preparation of 14C‐labeled vinyl chloride1975/01/01English4
Tritium labelling of compounds by exchange in strongly basic media1968/07/01English4
Synthesis of labeled anti‐inflammatory agents1973/04/01English4
Synthesis of dl‐erythro and threo‐sphingosine‐4,5‐3H1967/04/01English4
The synthesis of 14C‐diethylamine and lysergic acid diethylamide1974/04/01English4
Preparation of high specific activity DL‐tryptophan‐2, 3‐T and its resolution to l‐tryptophan‐2, 3‐T1973/04/01English4
A study of the stability and radiochemical purity of some radiopharmaceuticals. 1. Calculations of absorbed radiation energy1968/04/01English4
Synthesis of 3‐methyl‐4‐phenyl‐3‐butenamide‐1‐14C and N,N‐dideutero‐3‐methyl‐4‐phenyl‐3‐butenamide1974/01/01English4
A Method for routine preparation of very pure chlormerodrin labelled with 197 Hg or 203 Hg with high specific activity1972/10/01English4
The stability of thymidine, uridine and their related nucleotides, labelled with tritium1974/10/01English4
The synthesis of specifically 14C‐labelled 2,6‐diaminopimelic acid and its higher homologues1970/04/01English4
Synthesis of p‐substituted‐benzaldehyde‐α‐d1975/01/01English4
Markierte verbindungen VIII (1) tetrachloräthylen‐(14C) und tetrachlorkohlenstoff‐(14C)1971/04/01English4
Labelling of steroios by exchange with isotopic water on heterogeneous platinum and palladium: Methods for overcoming competing oxidation1975/01/01English4
Synthesis of O‐ethyl‐S‐phenyl‐14C(U)‐ethylphosphonodithioate1969/10/01English4
Synthesis of 14C‐labelled isotope‐isomeric alkanes. I n‐heptane‐1‐14C and ‐2‐14C1975/01/01English4
Synthesis of 7‐chloro‐1‐[cyclopropylmethyl‐(methylene‐14C)]‐5‐phenyl‐1H‐1,4‐benzodiazepin‐2 (3H)‐one and 7‐chloro‐1‐(cyclopropylmethyl)‐5‐phenyl‐1 H‐1,4‐benzodiazepin‐2 (3H)‐one‐5−14C1971/01/01English4
The synthesis of some pyrimidine derivatives labelled with 14C1970/01/01English4
Methyl esters of unsaturated fatty acids labeled with tritium in the methyl group1967/10/01English4
Isotopic discrimination between 3H and 14C in vitro during enzymatic phosphorylation of labelled thymidine1966/01/01English4
Synthesis of homovanillic acid‐2−14C, homoprotocatechuic acid‐2−14C, 3′, 4′‐dihydroxymandelic acid‐2−14C and 1‐(4 hydroxy‐3‐methoxyphenyl)‐ethylene glycol‐1−14C1971/10/01English4
L'Étude métabolique des médicaments marqués: Description d'un plan expérimental1966/04/01English4
Une nouvelle synthèse des cyanures alcalins marqués au carbone ‐14 par pyrolyse de la cyanamide de baryum en présence de sodium et d'oxyde de titane1968/01/01English4