淡江大學機構典藏:Item 987654321/19516
English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 62805/95882 (66%)
造訪人次 : 3982597      線上人數 : 573
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library & TKU Library IR team.
搜尋範圍 查詢小技巧:
  • 您可在西文檢索詞彙前後加上"雙引號",以獲取較精準的檢索結果
  • 若欲以作者姓名搜尋,建議至進階搜尋限定作者欄位,可獲得較完整資料
  • 進階搜尋
    請使用永久網址來引用或連結此文件: https://tkuir.lib.tku.edu.tw/dspace/handle/987654321/19516


    題名: 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
    貢獻者: 淡江大學化學學系
    日期: 1971-01
    上傳時間: 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
    顯示於類別:[化學學系暨研究所] 期刊論文

    文件中的檔案:

    檔案 描述 大小格式瀏覽次數
    0022-3263_36(11)p1459-1462.pdf625KbAdobe PDF380檢視/開啟
    Independent syntheses of the products of acid- and base-catalyzed rearrangements of 2-(1-isoquinolyl)-3,3,5-triarylpyrrolenines.pdf621KbAdobe PDF2檢視/開啟

    在機構典藏中所有的資料項目都受到原著作權保護.

    TAIR相關文章

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