Year |
Citation |
Score |
1990 |
Owen TC. Acidity constants of benzimidazolium ketone and pyridinium aldehyde hydrates Journal of Heterocyclic Chemistry. 27: 987-990. DOI: 10.1002/Jhet.5570270431 |
0.341 |
|
1979 |
Lopatin W, Young PR, Owen TC. Pyruvamides. 3. Involvement of the amide group in carbinolamine formation, gem-diamine formation, and transimination Journal of the American Chemical Society. 101: 960-969. DOI: 10.1021/Ja00498A027 |
0.441 |
|
1979 |
Lopatin W, Young PRJ, Owen TC. Pyruvamides. 3. Involvement Of The Amide Group In Carbinolamine Formation, Gem-Diamine Formation, And Transimination Cheminform. 10. DOI: 10.1002/Chin.197921156 |
0.323 |
|
1975 |
Young PR, Howell LG, Owen TC. Pyruvamide semicarbazone formation. Kinetics, mechanism, and pertinence to pyruvamide-dependent histidine decarboxylase. Journal of the American Chemical Society. 97: 6544-6551. PMID 1184869 DOI: 10.1021/Ja00855A043 |
0.416 |
|
1974 |
Owen TC, Young PR. Pyruvamide-promoted deamination and decarboxylation of amines and amino acids: a system modelling histidine decarboxylase. Febs Letters. 43: 308-312. PMID 4415413 DOI: 10.1016/0014-5793(74)80668-X |
0.451 |
|
1973 |
Owen TC, Ellis DR. Radiation-Induced Mixed-Disulfide Formation from Cystamine and Aliphatic Disulfides in Aqueous Solution Radiation Research. 53: 24-32. DOI: 10.2307/3573444 |
0.322 |
|
1972 |
Owen TC, Wilbraham AC. Glutathionesulfonic acid, the predominant product of x-radiolysis of air-saturated solutions of oxidized glutathione. Radiation Research. 50: 253-260. DOI: 10.2307/3573485 |
0.344 |
|
1972 |
Owen TC, Wilbraham AC, Roach JAG, Ellis DR. Reduced Products and Hydrogen from X-Irradiated Air-Saturated Solutions of Cystamine and Cystine Radiation Research. 50: 234-252. DOI: 10.2307/3573484 |
0.329 |
|
1971 |
Wilbraham AC, Owen TC, Johnson BG, Roach JA. Rapid photometric method for the determination of taurine and cysteic acid. Talanta. 18: 977-81. PMID 18960972 DOI: 10.1016/0039-9140(71)80160-1 |
0.338 |
|
1967 |
Owen TC, Wilbraham AC. The X-Radiolytic Destruction Of Lipoic Acid In Aqueous Solution: A Chain Reaction. Chemical Communications (London). 624-625. DOI: 10.1039/C19670000624 |
0.306 |
|
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