期刊文献+

合成肽在不对称催化反应中的应用

Application of Synthetic Peptides in Asymmetric Catalytic Reaction
下载PDF
导出
摘要 综述了合成肽作为催化剂在不对称催化反应中的应用,总结了各种合成肽催化剂的结构及其在催化不同类型反应如氰醇化反应、Strecker反应、Aldol反应、Michael加成反应、Morita-Baylis-Hillman反应和Stetter反应等中的催化活性及影响因素。 The application of synthetic peptides as catalyst in asymmetric catalytic reaction was reviewed.The structures and catalytic activities of the catalysts,and the influential factors for various asymmetric reactions such as hydrocyanation of aldehydes,asymmetric Strecker reaction,Aldol reaction,Michael addition reaction,Morita-Baylis-Hillman reaction and Stetter reaction were reviewed.
出处 《化学与生物工程》 CAS 2009年第11期7-11,共5页 Chemistry & Bioengineering
基金 教育部留学回国人员科研启动基金资助项目
关键词 合成肽 不对称催化 手性催化 synthetic peptide asymmetric catalysis chiral catalysis
  • 相关文献

参考文献35

  • 1Dugas H,Penney C. Bioorganic Chemistry: A Chemical Approach to Enzyme Action[EM]. New York: Springer-Verlag, 1981:93-94.
  • 2Jones J B. In Asymmetric Synthesis[M]. New York: Academic Press, 1985:309-310.
  • 3周中振,何彦祯,曹敏,杨光富.微波辅助组合合成的研究进展[J].有机化学,2006,26(11):1500-1507. 被引量:14
  • 4Oku J, ho N, Inoue S. Asymmetric cyanohydrin synthesis catalyzed by synthetic dipeptides. I . [J]. Die Makromolekulare Chemie,1979, 180(4) :1089-1091.
  • 5Oku J, Inoue S. Asymmetric cyanohydrin synthesis catalyzed by a synthetic cyclic dipeptide[J]. Journal of the Chemical Society, Chemical Communications, 1981, (5):229 -230.
  • 6Asada S,Kobayashi Y,Inoue S. Asymmetric addition of hydrogen cyanide to aliphatic aldehydes catalyzed by a synthetic cyclic peptide, cyclo[(S)-phenylalanyl-(S)-histidyl][J]. Die Makromolekulare Chemic,1985, 186(9) :1755 -1762.
  • 7Tanaka K, Mori A, Inoue S. The cyclic dipeptide cyclo[(S)-phenylalanyl-(S)-histidyl] as a catalyst for asymmetric addition of hydrogen cyanide to aldehydes[J]. The Journal of Organic Chemistry,1990, 55(1) :181-185.
  • 8Danda H. Essential factors in asymmetric hydrocyanation catalyzed by cyclo[-(R)-Phe-(R)-His-][J]. Synlett, 1991, (4) : 263- 264.
  • 9Iyer M S, Gigstad K M, Namdev N D, et al. Asymmetric catalysis of the Strecker amino acid synthesis by a cyclic dipeptide[J]. Journal of the American Chemical Society, 1996,118(20):4910- 4911.
  • 10Martin H J, List B. Mining sequence space for asymmetric amino catalysis: N-Terminal prolylpeptides efficiently catalyze enantioselective Aldol and Michael reactions [J]. Synlett, 2003, (12) : 1901-1902.

二级参考文献63

  • 1Ugi,I.; Dōmling,A.Endeavour 1994,18,115.
  • 2Hoel,A.M.L.; Nielsen,J.Tetrahedron Lett.1999,40,3941.
  • 3Brain,C.T.; Paul,J.M.; Loonc,Y.; Oakley,P.J.Tetrahedron Lett.1999,40,3275.
  • 4Brain,C.T.; Brunton,S.A.Synlett 2001,382.
  • 5Dolle,R.E.J.Comb.Chem.2000,2,383.
  • 6Dolle,R.E.J.Comb.Chem.2001,3,477.
  • 7Dolle,R.E.J.Comb.Chem.2002,4,369.
  • 8Maclean,D.; Baldwin,J.J.; Ivanov,V.T.; Kato,Y.; Shaw,A.; Schineider,P.; Gordon,E.M.J.Comb.Chem.2000,2,562.
  • 9Fenneri,H.Curr.Med.Chem.1996,3,343.
  • 10Cowley,P.M.; Rees,D.C.Curr.Med.Chem.1997,4,211.

共引文献13

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