期刊文献+

芳基高价碘与烯丙基硅烷的[3,3]-重排反应研究进展

Research progress on[3,3]-rearrangement reaction of aryl hypervalent iodine with allyl silane
下载PDF
导出
摘要 芳基高价碘作为反应物参与的[3,3]-重排反应逐渐受到合成化学家的关注.通过查阅高价碘与烯丙基硅烷反应的文献资料,并且分析、归纳后,进一步对高价碘与烯丙基硅烷的[3,3]-重排反应进行了深入的探讨与研究.详细阐述了该反应的发展历程,以及该反应在各类杂环化合物合成中的应用.随着高价碘化学的发展,高价碘与烯丙基硅烷的[3,3]-重排反应模型对[3,3]-重排领域具有非常重要的指导意义. Aryl iodine reagents serving as coupling partner in[3,3]-rearrangement had received great attention from synthetic community.The[3,3]-rearrangement reaction of hypervalent iodine and allyl silane was further discussed and studied through analysis and conclusion of the relevant literatures related hypervalent iodine and allyl substitution reactions.The history of the reaction and the application of the reaction in the synthesis of various heterocyclic compounds were described in details.With the development of hypervalent iodine chemistry,the hypervalent iodine and allyl silane[3,3]-rearrangement reaction model was supposed to have very important guiding significance for the[3,3]-rearrangement field.
作者 彭勃 陈孟源 詹娅玲 董涛涛 PENG Bo;CHEN Mengyuan;ZHAN Yaling;DONG Taotao(College of Chemistry and Life Sciences,Zhejiang Normal University,Jinhua 321004,China)
出处 《浙江师范大学学报(自然科学版)》 CAS 2020年第2期176-183,共8页 Journal of Zhejiang Normal University:Natural Sciences
基金 国家自然科学基金资助项目(21502171)。
关键词 高价碘 烯丙基硅烷 [3 3]-重排 三氟化硼乙醚 烯丙基化 hypervalent iodine allyl silane [3 3]-rearrangement boron trifluoride etherate allylation
  • 相关文献

参考文献1

二级参考文献35

  • 1Stang P J, Zhdankin V V. Organic polyvalent iodine compounds. Chemical Reviews, 1996, 96(3): 1123 1178.
  • 2Zhdankin V V, Stang P J. Recent developments in the chemistry of polyvalent iodine compounds. Chemical Reviews, 2002, 102(7): 2523 2584.
  • 3Zhdankin V V, Stang P J. Chemistry ofpolyvalent iodine. Chemical Reviews, 2008, 108(12): 5299-5358.
  • 4Ochiai M. Hypervalent halogans and their reactions in organic synthesis. Yakugaku Zasshi. Journal of the Pharmaceutical Society of Japan, 2009, 129(3): 321-334.
  • 5Zhdankin V V. Hypervalent iodine (III) reagents in organic synthesis. ARKIVOC, 2009, 1(1): 1-62.
  • 6Merritt E A, Olofsson B. ct-Functionalization of carbonyl com- pounds using hypervalent iodine reagents. Synthesis (Stuttgart), 2011, 4:517-538.
  • 7Silva L F Jr, Olofsson B. Hypervalent iodine reagents in the total synthesis of natural products. Na~'al Product Reports, 2011, 28 (10): 1722-1754.
  • 8Duschek A, Kirsch S F. 2 - Iodoxybenzoic acid--a simple oxidant with a dazzling array of potential applications. Angewandte Chemie International Edition, 2011, 50(7): 1524-1552.
  • 9Duschek A, Kirsch S. For an overview of IBX-mediated oxidations. Angewandte Chemie, 2011, 123:1562-1590.
  • 10Ochiai M, Ito T, Takaoka Y, Masaki Y. Generation of allenylio- dinanes and their reductive iodonio-Claisen rearrangement. Journal of the American Chemical Society, 1991, 113(4): 1319-1323.

共引文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部