Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Ignac, J."'
Autor:
Artemiou, P., Lukacin, S., Kirsch, P., Ignac, J., Bily, B., Tohatyova, A., Miroslava Rabajdova, Sabol, F.
Publikováno v:
Journal of Tehran University Heart Center, Vol 11, Iss 1 (2016)
The Journal of Tehran University Heart Center
Scopus-Elsevier
The Journal of Tehran University Heart Center
Scopus-Elsevier
Iatrogenic dissections of the ascending aorta are an uncommon and severe complication during cardiac catheterization. A 68-year-old female patient underwent diagnostic cardiac catheterization due to non-ST-elevation myocardial infarction. During the
Autor:
J. Bryan Jones, Ignac J. Jakovac
Publikováno v:
Organic Syntheses
Preparation of chiral, nonracemic γ-lactones by enzymecatalyzed oxidation of meso-diols: ( + )-(1R,6S)-8-oxabicyclo[4.3.0]nonan-7-one product: ( + )-(1R,6S)-8-oxabicyclo[4.3.0]nonan-7-one Keywords: annulation, heterocyclic-[5]; cyclization, oxidativ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::498088f417901ef5493590a37e6ec841
https://doi.org/10.1002/0471264180.os063.02
https://doi.org/10.1002/0471264180.os063.02
Publikováno v:
Canadian Journal of Chemistry; 1982, Vol. 60 Issue 15, p2007-2011, 5p
Autor:
Jones, J. Bryan, Jakovac, Ignac J.
Publikováno v:
Canadian Journal of Chemistry; 1982, Vol. 60 Issue 1, p19-28, 10p
Autor:
Ignac J. Jakovac, J. Bryan Jones
Publikováno v:
The Journal of Organic Chemistry. 44:2165-2168
Publikováno v:
Tetrahedron. 40:1235-1243
Further examples of the broad applicability of horse liver alcohol dehydrogenase-catalyzed oxidations of meso-diols as a route to chiral lactones of asymmetric synthetic value are described. The acyclic meso substrates, cis-2,3-dimethyl- and -diethyl
Publikováno v:
Journal of the American Chemical Society. 104:4659-4665
Autor:
Ignac J. Jakovac, J. Bryan Jones
Publikováno v:
Canadian Journal of Chemistry. 60:19-28
A new active site model for predicting and interpreting the structural- and stereospecificity of horse liver alcohol dehydrogenase-catalyzed oxidations and reductions has been formulated from the specificity, X-ray, and kinetic data now available. Th
Publikováno v:
Canadian Journal of Chemistry. 60:2007-2011
The synthesis of enantiomerically pure (+)-grandisol has been achieved from an enzymically generated chiral synthon. The synthesis is an efficient one, the yield of optically pure material being 12% up to the penultimate step and 3% overall.
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