Home > Conference materials > Papers > A novel, highly stereoselective synthetic approach for the preparation of substituted 2,5-dihydro-2,5-dihydroxyfurans
Original title:
A novel, highly stereoselective synthetic approach for the preparation of substituted 2,5-dihydro-2,5-dihydroxyfurans
Authors:
Jansa, Petr ; Kaiser, Martin Maxmilian ; Holý, Antonín ; Janeba, Zlatko Document type: Papers Conference/Event: Chemistry of Nucleic Acid Components /15./, Český Krumlov (CZ), 2011-06-05 / 2011-06-10
Year:
2011
Language:
eng Abstract:
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.
Keywords:
antiproliferative; nucleosides; stereoselective reduction Project no.: CEZ:AV0Z40550506 (CEP), 1M0508 (CEP) Funding provider: GA MŠk Host item entry: Chemistry of Nucleic Acid Components. 15th Symposium, ISBN 978-80-86241-37-1
Institution: Institute of Organic Chemistry and Biochemistry AS ČR
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Document availability information: Fulltext is available at the institute of the Academy of Sciences. Original record: http://hdl.handle.net/11104/0198504