aDepartment of Organic Chemistry, Institute of Chemical Technology, Prague, Czech Republic bInstitute of Microbiology, Academy of Science of the Czech Republic, Prague cInstitute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, Prague
Abstract:
The axially chiral ketone 1 and its methyl derivative 2 have been reduced with sodium borohydride to the corresponding diastereoisomeric alcohols 3 and 4.
Document Type:
Article
Language: English
Citation:
R. Kubik, J. Nemecek, S. Boehm, M. Hradilek, J. Kuthan, “Diastereoisomeric Imidazo[1,2-a]pyridines”, Mendeleev Commun., 5:1 (1995), 29–30
Linking options:
https://www.mathnet.ru/eng/mendc5021
https://www.mathnet.ru/eng/mendc/v5/i1/p29
This publication is cited in the following 3 articles:
Radek Pohl, Jan Sýkora, Petr Maloň, Stanislav Böhm, Bohumil Kratochvíl, Josef Kuthan, “Sterically Crowded Heterocycles. XIII. An Insight Into the Absolute Stereochemistry of Atropisomeric (Z)-3-(Imidazo[1,2-a]pyridin-3-yl)prop-2-en-1-ones”, Collect. Czech. Chem. Commun., 65:10 (2000), 1643
R. Pohl, J. Pawlas, S. Boehm, R. Hrabal, H. Dvorakova, J. Kuthan, “Atropisomeric and atropdiastereoisomeric 2-substituted 1-aryl-3,5-diphenylpyrroles”, Mendeleev Commun., 9:2 (1999), 74–76
R. KUBIK, J. NEMECEK, S. BOEHM, M. HRADILEK, J. KUTHAN, “ChemInform Abstract: Diastereoisomeric Imidazo(1,2‐a)pyridines.”, ChemInform, 26:26 (1995)