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Approach to the Synthesis of Dimeric Salen-Co(Ⅲ):A Recoverable Catalyst for Rac-Eprichlorohydrin HKR

Approach to the Synthesis of Dimeric Salen-Co(Ⅲ):A Recoverable Catalyst for Rac-Eprichlorohydrin HKR
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摘要 The synthesis of chiral dimeric Salen ligand 5, 5'-methylene-di-[(R, R )-| N-(3-tert-butylsalicylidine)-N'- ( 3', 5'-di- tert-butylsalicylidene) | - 1, 2-cyclohexanediamine ] which using 2-tert-butylphenol as starting material is reported. This compound reacts with cobalt (Ⅱ) acetate and then oxidized by air to give dimeric Salen catalyst 5 in this paper, which catalyzes the hydrolytic kinetic resolution (HKR) of racemic epichlorohydrin to afford biologically important chiral epoxides and diols. Ee values of diol up to 97 % were obtained, and the catalyst was recovered with no apparent loss. The synthesis of chiral dimeric Salen ligand 5, 5'-methylene-di-[(R, R )-| N-(3-tert-butylsalicylidine)-N'- ( 3', 5'-di- tert-butylsalicylidene) | - 1, 2-cyclohexanediamine ] which using 2-tert-butylphenol as starting material is reported. This compound reacts with cobalt (Ⅱ) acetate and then oxidized by air to give dimeric Salen catalyst 5 in this paper, which catalyzes the hydrolytic kinetic resolution (HKR) of racemic epichlorohydrin to afford biologically important chiral epoxides and diols. Ee values of diol up to 97 % were obtained, and the catalyst was recovered with no apparent loss.
出处 《Journal of Beijing Institute of Technology》 EI CAS 2008年第1期92-95,共4页 北京理工大学学报(英文版)
基金 Sponsored by the Beijing Municipal Science & Technology Commission Project (20070539022)
关键词 SALEN hydrolytic kinetic resolution asymmetric catalysis one pot process Salen hydrolytic kinetic resolution asymmetric catalysis one pot process
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参考文献10

  • 1Katsuki T.Some recent advances in metallosalen chem- istry[].Synlett.2003
  • 2Schaus S E,Larrow J F,Jacobsen E N.Practical syn- thesis of enantiopure cyclic 1,2-amino alcohols via catalyt- ic asymmetric ring opening of meso epoxides[].Journal of Organic Chemistry.1997
  • 3Kureshy RI,Khan N H,Abdi S HR,et al.Enantios- elective epoxidation of non-functionalized alkenes using a urea-hydrogen peroxide oxidant and a di meric homochi- ral Mn(Ⅲ)-Schiff base complex catalyst[].Tetrahe- dron: Asymmetry.2001
  • 4Tokunaga M,LarrowJ F,Kakiuchi F,et al.Asymmet- ric catalysis with water : Efficient kinetic resolution of terminal epoxides by means of catalytic hydrolysis[].Science.1997
  • 5Yoon T P,Jacobsen E N.Privileged chiral catalysts[].Science.2003
  • 6Breuer M,Ditrich K,Habicher T,et al.Industrial methods for the production of optically active intermedi- ates[].Angew ChemInt Ed.2004
  • 7David J.Homogeneous catalysis—Newapproaches to cat- alyst separation,recovery,and recycling[].Science.2003
  • 8Kureshy RI,Khan N H,Abdi S HR,et al.Si multane- ous production of chirally enriched epoxides and 1,2-diols from racemic epoxides via hydrolytic kinetic resolution (HKR)[].Journal of Molecular Catalysis A: Chemi- cal.2002
  • 9Whitney T A.Direct optical resolution of trans-1,2-di- aminocyclohexane from an amine mixture[].Journal of Organic Chemistry.1980
  • 10Casiraghi G,Casnati G,Puglia G,et al.Selective reac- tions between phenols and formaldehyde .A novel route to salicylaldehydes[].J C S PerkinⅠ.1980

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