期刊文献+

金催化去芳构化反应研究进展 被引量:16

Recent Progress on Gold-catalyzed Dearomatization Reactions
原文传递
导出
摘要 均相金催化在过去十几年经历了飞速的发展,展现出了非常高的催化效率和非常强的官能团兼容性.另一方面,催化去芳构化反应能够直接高效地将芳香化合物转化为高度官能团化的具有丰富三维立体结构的分子.因此,金催化去芳构化反应将会为天然产物和复杂分子的合成提供新颖直接高效的路径.本文总结了近几年金催化去芳构化反应的例子,主要可分为金催化的重排反应和炔烃/联烯的氢-官能团化反应两方面,同时还介绍了这两类反应的特点与可能的反应机理. Homogeneous gold catalysis has experienced rapid development since 2004 and generally exhibited high effi- ciency and good functional group tolerance. On the other hand, catalytic dearomatization reactions provide a unique and straight approach to the construction of highly functionalized molecules with diverse three-dimensional structures from sim- ple aromatic compounds. In this perspective, recent examples on gold-catalyzed dearomatization reactions are summarized in two main categories: gold-catalyzed rearrangements and gold-catalyzed hydrofunctionalizations of alkynes and allenes. In the first category, intra- and inter- molecular dearomatization reactions were achieved via gold-catalyzed rearrangements of pro- pargylic ester and its derivatives. Although this area is still at its early stage, several outstanding asymmetric examples have been reported by Shi and Toste. In the second category, an array of dearomatization reactions via gold-catalyzed hydrofunc- tionalizations of alkynes and allenes were presented. All these cases have shown great potentials for convenient and straight- forward construction of spiro and/or bridged polycyclic molecules, and some of them have exhibited excellent enantioselec- tivity. In addition, salient features and proposed mechanisms for these two types of reactions are also described.
出处 《化学学报》 SCIE CAS CSCD 北大核心 2017年第5期419-438,共20页 Acta Chimica Sinica
基金 科技部国家重点研发项目(2016YFA0202900) 国家基础研究计划(973项目2015CB856600) 国家自然科学基金委(21332009 21421091) 中国科学院战略性先导项目(XDB20000000) 中国科学院前沿科学重点研究项目(QYZDY-SSW-SLH012) 中国科学院国家外国专家局创新团队国际合作伙伴计划资助~~
关键词 金催化 去芳构化 不对称催化 重排反应 氢-官能团化反应 gold catalysis dearomatization asymmetric catalysis rearrangement hydrofunctionalization
  • 相关文献

参考文献7

二级参考文献47

  • 1蔡超君,胡炳成,吕春绪.吡咯及二氢吡咯类化合物的合成研究进展[J].有机化学,2005,25(10):1311-1317. 被引量:21
  • 2Schmidt,A.; Dreger,A. Curr. Org. Chem. 2011,15,1423.
  • 3Yu,X.; Zhang,J. Chem. Eur. J. 2012,18,12945.
  • 4Aggarwal,V. K.; de Vicente,J.; Bonnert,R. V. J. Org. Chem. 2003,68,5381.
  • 5Baldwin,J. E.; Pritchard,G. J.; Rathmell,R. E. J. Chem. Soc.,Perkin Trans. 1 2001,2906.
  • 6Chang,E.-M.; Lee,C. T.; Chen,C. Y.; Wong,F. F.; Yeh,M. Y. Aust. J. Chem. 2008,61,342.
  • 7Chang,K. T.; Choi,Y. H.; Kim,S. H.; Yoon,Y. J.; Lee,W. S. J. Chem. Soc.,Perkin Trans. 1 2002,207.
  • 8Deng,X.; Mani,N. S. J. Org. Chem. 2008,73,2412.
  • 9Fustero,S.; Sanchez-Rosello,M.; Barrio,P.; Simon-Fuentes,A. Chem. Rev. 2011,111,6984.
  • 10Garcia,H.; Iborra,S.; Miranda,M. A.; Morera,I. M.; Primo,J. Heterocycles 1991,32,1745.

共引文献33

同被引文献44

引证文献16

二级引证文献32

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