메뉴 건너뛰기




Volumn 28, Issue 4, 2010, Pages 272-278

Chemoenzymatic synthesis of enantiopure 1-phenyl-2-haloethanols and their esters

Author keywords

CALA; CALB; Enantiopure secondary alcohols; Enantiopure secondary esters; Kinetic resolution

Indexed keywords

ACYL DONORS; CANDIDA ANTARCTICA; CHEMO-ENZYMATIC SYNTHESIS; ENANTIOMERIC EXCESS; ENANTIOPURE; ENANTIOPURE SECONDARY ALCOHOLS; FASTER REACTIONS; GOOD YIELD; KINETIC RESOLUTION; NOVOZYM435; SECONDARY ALCOHOLS; VINYL ACETATES;

EID: 77954251714     PISSN: 10242422     EISSN: 10292446     Source Type: Journal    
DOI: 10.3109/10242422.2010.501406     Document Type: Article
Times cited : (11)

References (22)
  • 1
    • 0030250088 scopus 로고    scopus 로고
    • Calculation of enantiomer ratio and equilibrium constants in biocatalytic ping-pong bi-bi resolutions
    • Anthonsen HW, Hoff BH, Anthonsen T. 1996. Calculation of enantiomer ratio and equilibrium constants in biocatalytic ping-pong bi-bi resolutions. Tetrahedron: Asymmetry 7:2633-2638.
    • (1996) Tetrahedron: Asymmetry , vol.7 , pp. 2633-2638
    • Anthonsen, H.W.1    Hoff, B.H.2    Anthonsen, T.3
  • 2
    • 0032102791 scopus 로고    scopus 로고
    • Resolution of derivatives of 1,2-propanediol with lipase B from Candida antarctica. Effect of substrate structure, medium, water activity and acyl donor on enantiomeric ratio
    • Anthonsen T, Hoff BH. 1998. Resolution of derivatives of 1,2-propanediol with lipase B from Candida antarctica. Effect of substrate structure, medium, water activity and acyl donor on enantiomeric ratio. Chem Phys Lipids 93:199-207.
    • (1998) Chem Phys Lipids , vol.93 , pp. 199-207
    • Anthonsen, T.1    Hoff, B.H.2
  • 5
    • 4944241454 scopus 로고    scopus 로고
    • Enzymatic acylation reactions on ω-hydroxy cyanohydrins
    • de Gonzalo G, Lavandera I, Brieva R, Gotor V. 2004. Enzymatic acylation reactions on ω-hydroxy cyanohydrins. Tetrahedron 60:10525-10532.
    • (2004) Tetrahedron , vol.60 , pp. 10525-10532
    • De Gonzalo, G.1    Lavandera, I.2    Brieva, R.3    Gotor, V.4
  • 7
  • 8
    • 33646825361 scopus 로고    scopus 로고
    • New chiral building blocks from acetovanillone using lipases A and B from Candida antarctica
    • Fuglseth E, Anthonsen T, Hoff B. 2006. New chiral building blocks from acetovanillone using lipases A and B from Candida antarctica. Tetrahedron: Asymmetry 17:1290-1295.
    • (2006) Tetrahedron: Asymmetry , vol.17 , pp. 1290-1295
    • Fuglseth, E.1    Anthonsen, T.2    Hoff, B.3
  • 9
    • 50649093988 scopus 로고    scopus 로고
    • Asymmetric reduction using (R)-MeCBS and determination of absolute confi guration of para-substituted 2-fl uoroarylethanols
    • Fuglseth E, Sundby E, Bruheim P, Hoff BH. 2008a. Asymmetric reduction using (R)-MeCBS and determination of absolute confi guration of para-substituted 2-fl uoroarylethanols. Tetrahedron: Asymmetry 19:1941-1946.
    • (2008) Tetrahedron: Asymmetry , vol.19 , pp. 1941-1946
    • Fuglseth, E.1    Sundby, E.2    Bruheim, P.3    Hoff, B.H.4
  • 10
    • 45449084390 scopus 로고    scopus 로고
    • Electrophilic and nucleophilic side chain fl uorination of para-substituted acetop-henones
    • Fuglseth E, Krane Tvedt TH, Hoff B. 2008b. Electrophilic and nucleophilic side chain fl uorination of para-substituted acetop-henones. Tetrahedron 64:7318-7323.
    • (2008) Tetrahedron , vol.64 , pp. 7318-7323
    • Fuglseth, E.1    Krane Tvedt, T.H.2    Hoff, B.3
  • 11
    • 0001456022 scopus 로고    scopus 로고
    • A novel phosphinamide catalyst for the asymmetric reduction of ketones by borane
    • Gamble MP, Smith ARC, Wills M. 1998. A novel phosphinamide catalyst for the asymmetric reduction of ketones by borane. J Org Chem 63:6068-6071.
    • (1998) J Org Chem , vol.63 , pp. 6068-6071
    • Gamble, M.P.1    Arc, S.2    Wills, M.3
  • 12
    • 19444382313 scopus 로고    scopus 로고
    • Corrigendum to DMSO-triggered enhancement of enantioselectivity in Novozyme[435]-catalyzed transesterifi cation of chiral 1-phenylethanols
    • Goswami A, Goswami J. 2005. Corrigendum to DMSO-triggered enhancement of enantioselectivity in Novozyme[435]-catalyzed transesterifi cation of chiral 1-phenylethanols. Tetrahedron Lett 46:4411-4413.
    • (2005) Tetrahedron Lett , vol.46 , pp. 4411-4413
    • Goswami, A.1    Goswami, J.2
  • 14
    • 49449097238 scopus 로고    scopus 로고
    • The many roles for fl uorine in medicinal chemistry
    • Hagmann WK. 2008. The many roles for fl uorine in medicinal chemistry. J Med Chem 51:4359-4369.
    • (2008) J Med Chem , vol.51 , pp. 4359-4369
    • Hagmann, W.K.1
  • 16
    • 0032714332 scopus 로고    scopus 로고
    • Gas chromatographic enantiomer separation of C-3 and C-4 synthons: Prediction of absolute confi guration from elution order and enzymatic resolution
    • Hoff BH, Anthonsen T. 1999. Gas chromatographic enantiomer separation of C-3 and C-4 synthons: prediction of absolute confi guration from elution order and enzymatic resolution. Chirality 11:760-767.
    • (1999) Chirality , vol.11 , pp. 760-767
    • Hoff, B.H.1    Anthonsen, T.2
  • 17
    • 0034424913 scopus 로고    scopus 로고
    • Enantiopure derivatives of 1,2-alkanediols: Substrate requirements for lipase B from Candida antarctica
    • Jacobsen EE, Hoff BH, Anthonsen T. 2000. Enantiopure derivatives of 1,2-alkanediols: substrate requirements for lipase B from Candida antarctica. Chirality 12:654-659.
    • (2000) Chirality , vol.12 , pp. 654-659
    • Jacobsen, E.E.1    Hoff, B.H.2    Anthonsen, T.3
  • 18
    • 0036327837 scopus 로고    scopus 로고
    • Lipases from Candida antarctica: Unique biocatalysts from a unique origin
    • Kirk O, Christensen M W. 2002. Lipases from Candida antarctica: unique biocatalysts from a unique origin. Org Proc Res Dev 6: 446-451.
    • (2002) Org Proc Res Dev , vol.6 , pp. 446-451
    • Kirk, O.1    Christensen, M.W.2
  • 19
    • 18244393700 scopus 로고    scopus 로고
    • Kinetic resolution of 1-biaryl-and 1-(pyridylphenyl)alkan-1-ols catalyzed by the Lipase B from Candida antarctica
    • Kourist R, Gonzalez-Sabin J, Liz R, Rebolledo R. 2005. Kinetic resolution of 1-biaryl-and 1-(pyridylphenyl)alkan-1-ols catalyzed by the Lipase B from Candida antarctica. Adv Synth Catal 347:695-702.
    • (2005) Adv Synth Catal , vol.347 , pp. 695-702
    • Kourist, R.1    Gonzalez-Sabin, J.2    Liz, R.3    Rebolledo, R.4
  • 20
    • 1342264144 scopus 로고    scopus 로고
    • Synthesis of ether oligomers
    • Renaudet O, Reymond JL. 2004. Synthesis of ether oligomers. Org Lett 6:397-400.
    • (2004) Org Lett , vol.6 , pp. 397-400
    • Renaudet, O.1    Reymond, J.L.2
  • 22
    • 42249107322 scopus 로고    scopus 로고
    • Biocatalalytic resolution of saphenic acid. Substrate preferences for lipases A and B from Candida antarctica
    • Tjos å s F, Anthonsen T, Jacobsen EE. 2008. Biocatalalytic resolution of saphenic acid. Substrate preferences for lipases A and B from Candida antarctica. ARKIVOK vi:81-90.
    • (2008) ARKIVOK , vol.6 , pp. 81-90
    • Tjosås, F.1    Anthonsen, T.2    Jacobsen, E.E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.