期刊文献+

(S)-3-氯-1-苯基丙醇合成的两种方法的比较研究 被引量:5

Study on Two Synthesis Methods of (S)-3-chloro-1-phenylpropanol
下载PDF
导出
摘要 采用(S)-BINAP-Ru催化剂催化3-氯苯丙酮合成(S)构型的3-氯-1-苯基丙醇,收率75%,ee值99%。经生物筛选得到更为经济的生物催化剂胡萝卜活性胚芽,此生物组织具有还原3-氯苯丙酮活性,制备得到(S)-3-氯-1-苯基丙醇,产率78%,ee值98%。 (S)-BINAP-Ru as a catalyst was used in synthesis of (S)-3-chlorophenylpropanol from 3- chorophenylpropanone, the yield is 75% and ee is 99%. The good yield (78%) and high ee value (98%) is obtained when carrot's root used as a catalyst, find a more useful and economical biocatalyst.
出处 《浙江化工》 CAS 2010年第1期20-21,共2页 Zhejiang Chemical Industry
基金 浙江省重大科技攻关项目(2007C33047)
关键词 3-氯苯丙酮 (S)-3-氯-1-苯基丙醇 催化剂 3 -chloropropiophenone (S)-3-chloro- 1-phenylpropanol catalyst
  • 相关文献

参考文献3

  • 1赵妍,曹映玉,王万得,韩晓燕,杨琨,郝金库.氟西汀对映体的不对称合成[J].天津化工,2003,17(3):18-22. 被引量:3
  • 2Huang H L, Liu L T, Chen SF, et al. The synthesis of achiral fluoxetine intermediate by catalytic enantioselective hydrogenation of benzoylacetamide [J].Tetrahedron: Asymmetry, 1998, 9(10):1637-1640. 被引量:1
  • 3Ramachandran P V, Gong B Q, Brown Herbert C.Aremarkable inversion in configuration of the product alcohols from the asymmetric reduction of orthohydroxyacetophenones with β-chlorodiisopinocampheylborane, [J]. Tetrahedron Letters, 1994, 35(14) :2141-2144. 被引量:1

二级参考文献11

  • 1Manfred P Schneider, Ulrich Goergens. An efficient route to enantiomerically pure antidepressants: tomoxetine,nisoxetine and fluoxetine [ J ]. Tetrahedron Asymmetry,1992, (3) :525 - 528. 被引量:1
  • 2Paul N Devine, Richard M Heid. Stereoselective synthesis of 2 - aryloxy esters:an asymmetric approach to, tomoxetine and nisoxetine[J]. Tetrahedron, 1997, 53. 6739 -6746. 被引量:1
  • 3Y Gao, K B Sharpless. Asymmetric synthesis of both enantiomers of tomoxetine and fluoxetine. Selective reduction of 2, 3 - epoxycinnamly alcohol with Red - A1[J ]. J Org Chem, 1988,53: 4081 - 4084. 被引量:1
  • 4William H Miles, Elizabeth J Fialcowitz. Enantioselective synthesis of (S) - and (R) - fluoxetine hydrochloride[ J ]. Tetrahedron, 2001,57: 9925 - 9929. 被引量:1
  • 5E J Corey, Gregory A Reichard. Enantioselective and practical synthesis of R- and S- fluxoetine[ J ]. Tetrahedron Letters, 1989,30 : 5207 - 5210. 被引量:1
  • 6James W Hilborn, Zhi - Hui Lu. A practical asymmetric synthesis of (R) - fluxoetine and its major metabolite.(R) - norfluxoetine [ J ]. Tetrahedron Letters, 2001,42:8919- 8921. 被引量:1
  • 7Morris Srebnik,P V Ramachandran. A highly enantioselective synthesis of both optical isomers of tomoxetine,fluoxetine and nisoxetine [J ]. J Org Chern, 1988, 53:2916 - 2920. 被引量:1
  • 8Robert chenevert, genevieve fortier. Asymmetric synthesis of both enantiomers of fluoxetine via microbiological reduction of ethly benzoylacetate[J ]. Tetrahedron,1992,48: 6769 - 6776. 被引量:1
  • 9Margarita Quiros, Francisca Rebolledo. Enantioselective reduction of the β - keto amides by the fungus mortierella isabellina [ J ]. tetrahedron Asymmetry,1997, (8) :3035 - 3038. 被引量:1
  • 10Thomas M Koenig, David Mitchell. A convenient method for preparing enantiomerically pure nortluoxefine, fluoxetineand tomoxetine [ J ]. Tetrahedron Letters, 1994,35 : 1339 - 1342. 被引量:1

共引文献2

同被引文献31

引证文献5

二级引证文献15

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