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    Please use this identifier to cite or link to this item: http://tkuir.lib.tku.edu.tw:8080/dspace/handle/987654321/24965

    Title: Epoxidation of protected (1,4,5)-cyclohex-2-ene-triols and their acid hydrolysis to synthesize quercitols from D-(-)-quinic acid
    Authors: Shih, T. L.;Lin, Y. L.
    Contributors: 淡江大學化學學系
    Keywords: 1,4,5 cyclohex 2 ene triol derivative;butane 2,3 bisacetal;cyclohexene derivative;cyclohexylidene acetal;epoxide;quercitol;quinic acid;unclassified drug;article;chemical reaction kinetics;epoxidation;hydrolysis;stereochemistry;synthesis
    Date: 2005-07
    Issue Date: 2013-08-08 14:43:51 (UTC+8)
    Publisher: Philadelphia: Taylor & Francis Inc.
    Abstract: Highly stereoselective epoxidations have been achieved in both cyclohexylidene acetal and butane 2,3‐bisacetal (BBA) protection of (1,4,5)‐cyclohex‐2‐ene‐triols. These epoxy derivatives are all derived from D‐(−)‐quinic acid and can be used for the synthesis of muco‐, (+)‐epi‐, (+)‐vibo, (−)‐talo, and (−)‐gala‐quercitols.
    Relation: Synthetic Communications 35(13), pp.1809-1817
    DOI: 10.1081/SCC-200063960
    Appears in Collections:[化學學系暨研究所] 期刊論文

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