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An improved synthesis of 1-beta-D-arabinofuranosylcytosine 5 '-phosphate-L,1,2-diacylglycerols
Uppsala University.
1998 (English)In: NUCLEOSIDES & NUCLEOTIDES, ISSN 0732-8311, Vol. 17, no 9-11, 1953-1967 p.Article in journal (Other scientific) Published
Abstract [en]

5'-O-MMTr-cytosine arabinoside was prepared on a large scale from 5'-0-MMTr-cytidine with diphenyl carbonate via 5'-protected cytidine - 2',3'-carbonate -- aracytidine-2',2-anhydro derivative at a 67 % yield. The synthesis of 1,2-L-dipalmitoyl-sn-glycerol

Place, publisher, year, edition, pages
MARCEL DEKKER INC , 1998. Vol. 17, no 9-11, 1953-1967 p.
Keyword [en]
CYTOSINE-ARABINOSIDE; CHEMICAL SYNTHESIS; PROTECTING GROUP; 1;2-ISOPROPYLIDENE-SN-GLYCEROL; DIACYLGLYCEROLS; DERIVATIVES; LEUKEMIA; CELLS; ACID
Identifiers
URN: urn:nbn:se:uu:diva-27429OAI: oai:DiVA.org:uu-27429DiVA: diva2:55324
Note
Addresses: Nyilas A, Tisza L Krt 18-D, H-6720 Szeged, Hungary. Univ Uppsala, Ctr Biomed, Dept Bioorgan Chem, S-75123 Uppsala, Sweden.Available from: 2008-10-17 Created: 2008-10-17 Last updated: 2011-01-14

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