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Dodds, David R., Jones, J. Bryan. (1988) Enzymes in organic synthesis. 38. Preparations of enantiomerically pure chiral hydroxydecalones via stereospecific horse liver alcohol dehydrogenase catalyzed reductions of decalindiones. Journal Of The American Chemical Society, 110 (2) 577-583 doi:10.1021/ja00210a044

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Reference TypeJournal (article/letter/editorial)
TitleEnzymes in organic synthesis. 38. Preparations of enantiomerically pure chiral hydroxydecalones via stereospecific horse liver alcohol dehydrogenase catalyzed reductions of decalindiones
JournalJournal Of The American Chemical Society
AuthorsDodds, David R.Author
Jones, J. Bryan.Author
Year1988 (January)Volume110
Issue2
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ja00210a044Search in ResearchGate
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Mindat Ref. ID1427103Long-form Identifiermindat:1:5:1427103:4
GUID0
Full ReferenceDodds, David R., Jones, J. Bryan. (1988) Enzymes in organic synthesis. 38. Preparations of enantiomerically pure chiral hydroxydecalones via stereospecific horse liver alcohol dehydrogenase catalyzed reductions of decalindiones. Journal Of The American Chemical Society, 110 (2) 577-583 doi:10.1021/ja00210a044
Plain TextDodds, David R., Jones, J. Bryan. (1988) Enzymes in organic synthesis. 38. Preparations of enantiomerically pure chiral hydroxydecalones via stereospecific horse liver alcohol dehydrogenase catalyzed reductions of decalindiones. Journal Of The American Chemical Society, 110 (2) 577-583 doi:10.1021/ja00210a044
In(1988, January) Journal Of The American Chemical Society Vol. 110 (2) American Chemical Society (ACS)

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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
Bridges, Alexander J., Raman, P. Sundara, Ng, George S. Y., Jones, J. Bryan (1984) Enzymes in organic synthesis. 31. Preparations of enantiomerically pure bicyclic [3.2.1] and [3.3.1] chiral lactones via stereospecific horse liver alcohol dehydrogenase catalyzed oxidations of meso diols. Journal Of The American Chemical Society, 106 (5) 1461-1467 doi:10.1021/ja00317a046
Lok, Kar P., Jakovac, Ignac J., Jones, J. Bryan (1985) Enzymes in organic synthesis. 34. Preparations of enantiomerically pure exo- and endo-bridged bicyclic [2.2.1] and [2.2.2] chiral lactones via stereospecific horse liver alcohol dehydrogenase catalyzed oxidations of meso diols. Journal Of The American Chemical Society, 107 (8) 2521-2526 doi:10.1021/ja00294a052
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
Davies, John, Jones, J. Bryan (1979) Enzymes in organic synthesis. 16. Heterocyclic ketones as substrates of horse liver alcohol dehydrogenase. Stereospecific reductions of 2-substituted tetrahydrothiopyran-4-ones. Journal Of The American Chemical Society, 101 (18) 5405-5410 doi:10.1021/ja00512a048
LOK, K. P., JAKOVAC, I. J., JONES, J. B. (1985) ChemInform Abstract: ENZYMES IN ORGANIC SYNTHESIS. 34. PREPARATIONS OF ENANTIOMERICALLY PURE EXO- AND ENDO-BRIDGED BICYCLIC (2.2.1) AND (2.2.2) CHIRAL LACTONES VIA STEREOSPECIFIC HORSE LIVER ALCOHOL DEHYDROGENASE CATALYZED OXIDATIONS OF MESO DIOLS. Chemischer Informationsdienst, 16 (34) doi:10.1002/chin.198534201
BRIDGES, A. J., RAMAN, P. S., NG, G. S. Y., JONES, J. B. (1984) ChemInform Abstract: ENZYMES IN ORGANIC SYNTHESIS. 31. PREPARATIONS OF ENANTIOMERICALLY PURE BICYCLIC (3.2.1) AND (3.3.1) CHIRAL LACTONES VIA STEREOSPECIFIC HORSE LIVER ALCOHOL DEHYDROGENASE CATALYZED OXIDATIONS OF MESO DIOLS. Chemischer Informationsdienst, 15 (24) doi:10.1002/chin.198424231
Haslegrave, J. Anthony, Jones, J. Bryan (1982) Enzymes in organic synthesis. 25. Heterocyclic ketones as substrates of horse liver alcohol dehydrogenase. Highly stereoselective reductions of 2-substituted tetrahydropyran-4-ones. Journal Of The American Chemical Society, 104 (17) 4666-4671 doi:10.1021/ja00381a025
NG, G. S. Y., YUAN, L.-C., JAKOVAC, I. J., JONES, J. B. (1984) ChemInform Abstract: ENZYMES IN ORGANIC SYNTHESIS - 29. PREPARATIONS OF ENANTIOMERICALLY PURE CIS-2,3- AND 2,4-DIMETHYL LACTONES VIA HORSE LIVER ALCOHOL DEHYDROGENASE-CATALYZED OXIDATIONS. Chemischer Informationsdienst, 15 (35) doi:10.1002/chin.198435352
Jones, J. Bryan, Dodds, David R. (1987) Enzymes in organic synthesis. 37. Preparation and characterization of potential decalindione substrates of horse liver alcohol dehydrogenase. Canadian Journal of Chemistry, 65 (10). 2397-2404 doi:10.1139/v87-400
Jones, J. Bryan, Dodds, David R. (1979) Enzymes in organic synthesis 17. Oxidoreductions of alcohols, aldehydes, and ketones using chemically modified horse liver alcohol dehydrogenase. Canadian Journal of Chemistry, 57 (19). 2533-2538 doi:10.1139/v79-406
 
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