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
Аннотация:
The axially chiral ketone 1 and its methyl derivative 2 have been reduced with sodium borohydride to the corresponding diastereoisomeric alcohols 3 and 4.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
R. Kubik, J. Nemecek, S. Boehm, M. Hradilek, J. Kuthan, “Diastereoisomeric Imidazo[1,2-a]pyridines”, Mendeleev Commun., 5:1 (1995), 29–30
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc5021
https://www.mathnet.ru/rus/mendc/v5/i1/p29
Эта публикация цитируется в следующих 3 статьяx:
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)
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