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    Please use this identifier to cite or link to this item: http://ir.lib.ncu.edu.tw/handle/987654321/28333


    Title: Reduction of 1-pyrrolyl and 1-indolyl carbamates to hemiaminals
    Authors: Hsu,HC;Hou,DR
    Contributors: 中央大學
    Keywords: NUCLEAR-MAGNETIC-RESONANCE;DERIVATIVES;PYRROLE;INDOLE;ALKALOIDS;ANALOGS
    Date: 2009
    Issue Date: 2010-06-29 19:46:19 (UTC+8)
    Publisher: 化學研究所
    Abstract: Hemiaminals of pyrroles and indoles have been prepared from the lithium aluminum hydride reduction of 1-pyrrolyl and 1-indolyl carbamates with good yields (67-82%). These carbamates are more reactive than aliphatic amides and carbamates under the LAH reduction, but less reactive than esters. (c) 2009 Elsevier Ltd. All rights reserved.
    Relation: TETRAHEDRON LETTERS
    Appears in Collections:[化學研究所] 期刊論文

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