期刊文献+

苯丙氨酸锂催化醛和胺以及三甲基硅腈三组分的Strecker反应(英文)

Three-component Strecker reaction of aldehyde,amine and trimethylsilyl cyanide catalyzed by phenylalanine lithium
下载PDF
导出
摘要 以苯丙氨基酸锂为催化剂,成功催化了醛、胺和三甲基硅腈三组分的Strecker反应,并结合一系列氨基酸盐催化剂的筛选以及各种溶剂的选择优化了反应条件.结果表明,利用所述反应可以得到较高收率的α-氨基腈;该三组份的Strecker反应具有反应条件温和、反应收率较高、操作简便、无需繁琐的分离步骤、催化剂便宜且环境友好等优点. The three-component Strecker reaction of aldehyde, amine and trimethyl silyl cyanide was successfully carried out with L-phenylalanine lithium as the catalyst. The reaction conditions were optimized in relation to the screening of a series of amino acid salt catalysts and the selection of various solvents. Results indicate that the present reaction can be adopted to Obtain a-amino nitriles in good yields. Furthermore, the protocol has the advantages of mild reaction conditions, good yield, simple operation, easy separation, and inexpensive and environmentally benign catalyst.
出处 《化学研究》 CAS 2014年第1期37-40,共4页 Chemical Research
基金 National Natural Science Foundation of China(21272109)
关键词 苯丙氨基酸锂 三甲基硅腈 三组分Strecker反应 phenylalanine lithium aldehyde amine trimethylsilyl cyanide three-component Strecker reaction
  • 相关文献

参考文献7

  • 1JARUSIEWICZ J,CHOE Y,YOO K S. Efficient three-component Strecker reaction of aldehydes/ketones via NHC-amidate palladium(Ⅱ) complex catalysis[J].Journal of Organic Chemistry,2009,(07):2873-2876.
  • 2SURYA PRAKASH G K,MATHEW T,OLAH G A. Gallium(Ⅲ) triflate:an efficient and a sustainable Lewis acid catalyst for organic synthetic transformations[J].Accounts of Chemical Research,2012,(04):565-577.
  • 3LIU Yan,MO Yan,CUI Yong. Porous and robust lanthanide metal-organoboron frameworks as water tolerant Lewis acid catalysts[J].Inorganic Chemistry,2013,(18):10286-10291.
  • 4YAMAGUCHI M,YOKOTA N,MINAMI T. The michael addition of dimethyl malonate to α,β-unsaturated aldehydes catalyzed by proline lithium salt[J].Journal of the Chemical Society Chemical Communications,1991,(16):1088-1089.
  • 5YAMAGUCHI M,SHIRAISHI T,HIRAMA M. Asymmetric michael addition of malonate anions to prochiral acceptors catalyzed by L-proline rubidium salt[J].Journal of Organic Chemistry,1996,(10):3520-3530.
  • 6YOSHIDA M,SATO A,HARA S. Asymmetric michael addition of aldehydes to nitroalkenes using a primary amino acid lithium salt[J].Organic and Biological Chemistry,2010.3031-3036.
  • 7YOSHIDA M,NARITA M,HARA S. Asymmetric michael addition of malonates to enones catalyzed by a primary β-amino acid and its lithium salt[J].Journal of Organic Chemistry,2011.8513-8517.

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