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Jones, J. Bryan, Goodbrand, H. Bruce (1977) Regiospecific horse liver alcohol dehydrogenase-catalyzed oxidations of some bishydroxycyclohexanes. Canadian Journal of Chemistry, 55 (14). 2685-2691 doi:10.1139/v77-374

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Reference TypeJournal (article/letter/editorial)
TitleRegiospecific horse liver alcohol dehydrogenase-catalyzed oxidations of some bishydroxycyclohexanes
JournalCanadian Journal of Chemistry
AuthorsJones, J. BryanAuthor
Goodbrand, H. BruceAuthor
Year1977 (July 15)Volume55
Issue14
PublisherCanadian Science Publishing
DOIdoi:10.1139/v77-374Search in ResearchGate
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Mindat Ref. ID8303530Long-form Identifiermindat:1:5:8303530:4
GUID0
Full ReferenceJones, J. Bryan, Goodbrand, H. Bruce (1977) Regiospecific horse liver alcohol dehydrogenase-catalyzed oxidations of some bishydroxycyclohexanes. Canadian Journal of Chemistry, 55 (14). 2685-2691 doi:10.1139/v77-374
Plain TextJones, J. Bryan, Goodbrand, H. Bruce (1977) Regiospecific horse liver alcohol dehydrogenase-catalyzed oxidations of some bishydroxycyclohexanes. Canadian Journal of Chemistry, 55 (14). 2685-2691 doi:10.1139/v77-374
In(1977, July) Canadian Journal of Chemistry Vol. 55 (14) Canadian Science Publishing

See Also

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Irwin, Anthony J., Jones, J. Bryan (1977) Regiospecific and enantioselective horse liver alcohol dehydrogenase catalyzed oxidations of some hydroxycyclopentanes. Journal Of The American Chemical Society, 99 (5) 1625-1630 doi:10.1021/ja00447a057
IRWIN, A. J., JONES, J. B. (1977) ChemInform Abstract: REGIOSPECIFIC AND ENANTIOSELECTIVE HORSE LIVER ALCOHOL DEHYDROGENASE CATALYZED OXIDATIONS OF SOME HYDROXYCYCLOPENTANES. Chemischer Informationsdienst, 8 (21) doi:10.1002/chin.197721121
Jones, J. Bryan, Lok, Kar P. (1979) Enzymes in organic synthesis. 14. Stereoselective horse liver alcohol dehydrogenase catalyzed oxidations of diols containing a prochiral centre and of related hemiacetals. Canadian Journal of Chemistry, 57 (9). 1025-1032 doi:10.1139/v79-170
Jakovac, Ignac J., Goodbrand, H. Bruce, Lok, Kar P., Jones, J. Bryan (1982) Enzymes in organic synthesis. 24. Preparations of enantiomerically pure chiral lactones via stereospecific horse liver alcohol dehydrogenase catalyzed oxidations of monocyclic meso diols. Journal Of The American Chemical Society, 104 (17) 4659-4665 doi:10.1021/ja00381a024
Jones, J. Bryan, Francis, Christopher J. (1984) Enzymes in organic synthesis. 32. Stereospecific horse liver alcohol dehydrogenase-catalyzed oxidations of exo- and endo-oxabicyclic meso diols. Canadian Journal of Chemistry, 62 (11). 2578-2582 doi:10.1139/v84-440
Irwin, Anthony J., Jones, J. Bryan (1977) Asymmetric syntheses via enantiotopically selective horse liver alcohol dehydrogenase catalyzed oxidations of diols containing a prochiral center. Journal Of The American Chemical Society, 99 (2) 556-561 doi:10.1021/ja00444a040
Jones, J. Bryan, Jakovac, Ignac J. (1982) A new cubic-space section model for predicting the specificity of horse liver alcohol dehydrogenase-catalyzed oxidoreductions. Canadian Journal of Chemistry, 60 (1). 19-28 doi:10.1139/v82-005
Jones, J. Bryan, Schwartz, Harold M. (1982) Enzymes in organic synthesis. 22. Effects of organic solvents on horse liver alcohol dehydrogenase-catalyzed reduction. Canadian Journal of Chemistry, 60 (3). 335-338 doi:10.1139/v82-051
Jones, J. Bryan, Schwartz, Harold M. (1982) Enzymes in organic synthesis. 23. Effects of organic solvents on horse liver alcohol dehydrogenase-catalyzed oxidation. Canadian Journal of Chemistry, 60 (8). 1030-1033 doi:10.1139/v82-152
JAKOVAC, I. J., GOODBRAND, H. B., LOK, K. P., JONES, J. B. (1982) ChemInform Abstract: ENZYMES IN ORGANIC SYNTHESIS. 24. PREPARATIONS OF ENANTIOMERICALLY PURE CHIRAL LACTONES VIA STEREOSPECIFIC HORSE LIVER ALCOHOL DEHYDROGENASE CATALYZED OXIDATIONS OF MONOCYCLIC MESO DIOLS. Chemischer Informationsdienst, 13 (47) doi:10.1002/chin.198247363
Jones, J. Bryan, Takemura, Tetsuo (1982) Enzymes in organic synthesis. 28. Reinvestigation of the horse liver alcohol dehydrogenase-catalyzed reductions of 2-alkylcyclohexanones.Identification of cis-alkylcyclohexanols as minor products. Canadian Journal of Chemistry, 60 (23). 2950-2956 doi:10.1139/v82-423
 
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