English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 54134/88902 (61%)
造访人次 : 10552593      在线人数 : 22
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library & TKU Library IR team.
搜寻范围 查询小技巧:
  • 您可在西文检索词汇前后加上"双引号",以获取较精准的检索结果
  • 若欲以作者姓名搜寻,建议至进阶搜寻限定作者字段,可获得较完整数据
  • 进阶搜寻


    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: http://tkuir.lib.tku.edu.tw:8080/dspace/handle/987654321/19516


    题名: Independent syntheses of the products of acid- and base-catalyzed rearrangements of 2-(1-isoquinolyl)-3,3,5-triarylpyrrolenines
    作者: McEwen, William E.;Berkeile, David H.;Liao, Tsung-kai;林雲山;Lin, Yun-shan
    贡献者: 淡江大學化學學系
    日期: 1971-01
    上传时间: 2009-11-04 16:51:55 (UTC+8)
    出版者: Washington: American Chemical Society (ACS)
    摘要: 2-( l-Isoquinoly1)-3,4,5- triphenylpyrrole (4) and 2-( l-isoquinolyl)-3-p-anisyl-4,5-diphenylpyrrole (6) have been synthesized by unambiguous methods. The synthetic samples are identical with the products of the acid- or base-catalyzed isomerization of 2-( l-isoquinolyl)-3,3,5-triphenylpyrrolenine (3) and the base-catalyzed isomerization of 2-( l-isoquinolyl)-3-p-anisyl-3,5-diphenylpyrro1eni(n2e l ), respectively. By inference, 2-( 1-isoquinoly1)- 4-p-ani~yl-3~5-diphenylpyrro(l7e) is the product of the acid-catalyzed isomerization of 2 1. These facts provide additional support for the mechanisms of the isomerization reactions proposed in previous papers.
    關聯: Journal of Organic Chemistry 36(11), pp.1459-1462
    DOI: 10.1021/jo00810a003
    显示于类别:[化學學系暨研究所] 期刊論文

    文件中的档案:

    档案 描述 大小格式浏览次数
    0022-3263_36(11)p1459-1462.pdf625KbAdobe PDF296检视/开启

    在機構典藏中所有的数据项都受到原著作权保护.

    TAIR相关文章

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library & TKU Library IR teams. Copyright ©   - 回馈