Počet záznamů: 1
A novel, highly stereoselective synthetic approach for the preparation of substituted 2,5-dihydro-2,5-dihydroxyfurans
- 1.0361097 - ÚOCHB 2012 CZ eng C - Konferenční příspěvek (zahraniční konf.)
Jansa, Petr - Kaiser, Martin Maxmilian - Holý, Antonín - Janeba, Zlatko
A novel, highly stereoselective synthetic approach for the preparation of substituted 2,5-dihydro-2,5-dihydroxyfurans.
Chemistry of Nucleic Acid Components. 15th Symposium. Praha: Institute of Organic Chemistry and Biochemistry AS CR, v. v. i., 2011 - (Hocek, M.), s. 339-341. Collection Symposium Series, 12. ISBN 978-80-86241-37-1.
[Chemistry of Nucleic Acid Components /15./. Český Krumlov (CZ), 05.06.2011-10.06.2011]
Grant CEP: GA MŠMT 1M0508
Výzkumný záměr: CEZ:AV0Z40550506
Klíčová slova: stereoselective reduction * nucleosides * antiproliferative
Kód oboru RIV: CC - Organická chemie
A novel highly stereoselective reduction of 5-substituted furan-2(5H)-ones has been developed as a key step in the synthesis of 2,5-dihydro-5-hydroxyfuran-2-yl nucleosides.
Trvalý link: http://hdl.handle.net/11104/0198504
Počet záznamů: 1