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A novel, highly stereoselective synthetic approach for the preparation of substituted 2,5-dihydro-2,5-dihydroxyfurans
- 1.0361097 - ÚOCHB 2012 CZ eng C - Conference Paper (international conference)
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]
R&D Projects: GA MŠMT 1M0508
Institutional research plan: CEZ:AV0Z40550506
Keywords : stereoselective reduction * nucleosides * antiproliferative
Subject RIV: CC - Organic Chemistry
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.
Permanent Link: http://hdl.handle.net/11104/0198504
Number of the records: 1