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May, Sheldon W., Phillips. Robert S., (1980) Asymmetric sulfoxidation by dopamine .beta.-hydroxylase, an oxygenase heretofore considered specific for methylene hydroxylation. Journal Of The American Chemical Society, 102 (18) 5981-5983 doi:10.1021/ja00538a080

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Reference TypeJournal (article/letter/editorial)
TitleAsymmetric sulfoxidation by dopamine .beta.-hydroxylase, an oxygenase heretofore considered specific for methylene hydroxylation
JournalJournal Of The American Chemical Society
AuthorsMay, Sheldon W.Author
Phillips. Robert S., Author
Year1980 (August)Volume102
Issue18
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ja00538a080Search in ResearchGate
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Mindat Ref. ID1363128Long-form Identifiermindat:1:5:1363128:4
GUID0
Full ReferenceMay, Sheldon W., Phillips. Robert S., (1980) Asymmetric sulfoxidation by dopamine .beta.-hydroxylase, an oxygenase heretofore considered specific for methylene hydroxylation. Journal Of The American Chemical Society, 102 (18) 5981-5983 doi:10.1021/ja00538a080
Plain TextMay, Sheldon W., Phillips. Robert S., (1980) Asymmetric sulfoxidation by dopamine .beta.-hydroxylase, an oxygenase heretofore considered specific for methylene hydroxylation. Journal Of The American Chemical Society, 102 (18) 5981-5983 doi:10.1021/ja00538a080
In(1980, August) Journal Of The American Chemical Society Vol. 102 (18) American Chemical Society (ACS)

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MAY, S. W., PHILLIPS, R. S. (1980) ChemInform Abstract: ASYMMETRIC SULFOXIDATION BY DOPAMINE β-HYDROXYLASE, AN OXYGENASE HERETOFORE CONSIDERED SPECIFIC FOR METHYLENE HYDROXYLATION. Chemischer Informationsdienst, 11 (48) doi:10.1002/chin.198048115
Sirimanne, Sarath R., May, Sheldon W. (1988) Facile stereoselective allylic hydroxylation by dopamine .beta.-monooxygenase. Journal Of The American Chemical Society, 110 (22) 7560-7561 doi:10.1021/ja00230a059
Bachan, L., Storm, C. B., Wheeler, J. W., Kaufman, S. (1974) Isotope effects in the hydroxylation of phenylethylamine by dopamine .beta.-hydroxylase. Journal Of The American Chemical Society, 96 (21) 6799-6800 doi:10.1021/ja00828a063
Katopodis, Andreas G., Smith, Homer A., May, Sheldon W. (1988) New oxyfunctionalization capabilities for .omega.-hydroxylases. Asymmetric aliphatic sulfoxidation and branched ether demethylation. Journal Of The American Chemical Society, 110 (3) 897-899 doi:10.1021/ja00211a033
Wimalasena, Kandatege, May, Sheldon W. (1987) Mechanistic studies on dopamine .beta.-monooxygenase catalysis: N-dealkylation and mechanism-based inhibition by benzylic-nitrogen-containing compounds. Evidence for a single-electron-transfer mechanism. Journal Of The American Chemical Society, 109 (13) 4036-4046 doi:10.1021/ja00247a033
Wimalasena, Kandatege, May, Sheldon W. (1989) Dopamine .beta.-monooxygenase-catalyzed aromatization of 1-(2-aminoethyl)-1,4-cyclohexadiene: redirection of specificity and evidence for a hydrogen-atom-transfer mechanism. Journal Of The American Chemical Society, 111 (7) 2729-2731 doi:10.1021/ja00189a065
BACHAN, L., STORM, C. B., WHEELER, J. W., KAUFMAN, S. (1974) ChemInform Abstract: ISOTOPE EFFECTS IN THE HYDROXYLATION OF PHENYLETHYLAMINE BY DOPAMINE BETA-HYDROXYLASE. Chemischer Informationsdienst, 5 (52) doi:10.1002/chin.197452194
Kelly, T. Ross, Vaya, Jacob, Ananthasubramanian, L. (1980) Efficient, regiospecific synthesis of (.+-.)-daunomycinone. Journal Of The American Chemical Society, 102 (18) 5983-5984 doi:10.1021/ja00538a081
BATTERSBY, A. R., SHELDRAKE, P. W., STAUNTON, J., WILLIAMS, D. C. (1974) ChemInform Abstract: STEREOCHEMICAL COURSE OF HYDROXYLATION OF DOPAMINE BY DOPAMINE-BETA-HYDROXYLASE (EC1.14.17.1) Chemischer Informationsdienst, 5 (43) doi:10.1002/chin.197443187
Itoh, Shinobu, Kondo, Toshihiko, Komatsu, Mitsuo, Ohshiro, Yoshiki, Li, Chunmin, Kanehisa, Nobuko, Kai, Yasushi, Fukuzumi, Shunichi (1995) Functional Model of Dopamine .beta.-Hydroxylase. Quantitative Ligand Hydroxylation at the Benzylic Position of a Copper Complex by Dioxygen. Journal Of The American Chemical Society, 117 (16) 4714-4715 doi:10.1021/ja00121a033
May, Sheldon W., Schwartz, Robert D. (1974) Stereoselective epoxidation of octadiene catalyzed by an enzyme system of Pseudomonas oleovorans. Journal Of The American Chemical Society, 96 (12) 4031-4032 doi:10.1021/ja00819a060
 
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