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    Please use this identifier to cite or link to this item: http://tkuir.lib.tku.edu.tw:8080/dspace/handle/987654321/24869

    Title: Chemoselective deprotection of acid labile primary hydroxyl protecting groups under CBr4-photoirradiation conditions
    Authors: 李世元;Lee, Adam Shih-yuan;Chen, M. Y.;Patkar, L. N.;Lu, K. C.;Lin, C. C.
    Contributors: 淡江大學化學學系
    Keywords: CBr4-photoirradiation;Deprotection
    Date: 2004-12-06
    Issue Date: 2009-12-01
    Publisher: Elsevier
    Abstract: The CBr4-photoirradiation in methanol generates a controlled source of HBr, which can chemoselectively deprotect commonly used hydroxyl-protecting groups in saccharides and nucleosides, such as tert-butyldimethylsilyl, isopropylidene, benzylidene and triphenyl ethers in the presence of other acid-labile functional groups.
    Relation: Tetrahedron 60(50), pp.11465-11475
    DOI: 10.1016/j.tet.2004.09.095
    Appears in Collections:[化學學系暨研究所] 期刊論文

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