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Volumn 100, Issue 9, 2009, Pages 2463-2468

Adzuki bean: A new resource of biocatalyst for asymmetric reduction of aromatic ketones with high stereoselectivity and substrate tolerance

Author keywords

Adzuki bean; Asymmetric reduction; Biocatalyst; Phaseolus angularis; Substrate tolerance

Indexed keywords

ADZUKI BEAN; ASYMMETRIC REDUCTION; BIOCATALYST; PHASEOLUS ANGULARIS; SUBSTRATE TOLERANCE;

EID: 59649104098     PISSN: 09608524     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.biortech.2008.11.054     Document Type: Article
Times cited : (39)

References (24)
  • 1
    • 0347355224 scopus 로고    scopus 로고
    • Highly stereoselective reduction of 4-aryl-2-oxo but-3-enoic carboxylic esters by plant cell culture of Daucus carota
    • Baskar B., Ganesh S., Lokeswari T.S., and Chadha A. Highly stereoselective reduction of 4-aryl-2-oxo but-3-enoic carboxylic esters by plant cell culture of Daucus carota. J. Mol. Catal. B: Enzymatic 27 (2004) 13-17
    • (2004) J. Mol. Catal. B: Enzymatic , vol.27 , pp. 13-17
    • Baskar, B.1    Ganesh, S.2    Lokeswari, T.S.3    Chadha, A.4
  • 2
    • 33745069991 scopus 로고    scopus 로고
    • Daucus carota L. Mediated bioreduction of prochiral ketones
    • Blanchard N., and Van de Weghe P. Daucus carota L. Mediated bioreduction of prochiral ketones. Org. Biomol. Chem. 4 (2006) 2348-2353
    • (2006) Org. Biomol. Chem. , vol.4 , pp. 2348-2353
    • Blanchard, N.1    Van de Weghe, P.2
  • 3
    • 0035861701 scopus 로고    scopus 로고
    • High enantioselectivity and broad substrate specificity of a carbonyl reductase: toward a versatile biocatalyst
    • Ema T., Moriya H., Kofukuda T., Ishida T., Maehara K., Utaka M., and Sakai T. High enantioselectivity and broad substrate specificity of a carbonyl reductase: toward a versatile biocatalyst. J. Org. Chem. 66 (2001) 8682-8684
    • (2001) J. Org. Chem. , vol.66 , pp. 8682-8684
    • Ema, T.1    Moriya, H.2    Kofukuda, T.3    Ishida, T.4    Maehara, K.5    Utaka, M.6    Sakai, T.7
  • 4
    • 4344665227 scopus 로고    scopus 로고
    • Synthetic applicability and in situ recycling of a B-methoxy oxazaborolidine catalyst derived from cis-1-amino-indan-2-ol
    • Gilmore N.J., Jones S., and Muldowney M.P. Synthetic applicability and in situ recycling of a B-methoxy oxazaborolidine catalyst derived from cis-1-amino-indan-2-ol. Org. Lett. 6 (2004) 2805-2808
    • (2004) Org. Lett. , vol.6 , pp. 2805-2808
    • Gilmore, N.J.1    Jones, S.2    Muldowney, M.P.3
  • 5
    • 0348225170 scopus 로고    scopus 로고
    • Rapid identification of enantioselective ketone reductions using targeted microbial libraries
    • Homann M.J., Vail R.B., Previte E., Tamarez M., Morgan B., Dodds D.R., and Zaks A. Rapid identification of enantioselective ketone reductions using targeted microbial libraries. Tetrahedron 60 (2004) 789-797
    • (2004) Tetrahedron , vol.60 , pp. 789-797
    • Homann, M.J.1    Vail, R.B.2    Previte, E.3    Tamarez, M.4    Morgan, B.5    Dodds, D.R.6    Zaks, A.7
  • 7
    • 0038539459 scopus 로고    scopus 로고
    • Soaked Phaseolus aureus L: an efficient biocatalyst for asymmetric reduction of prochiral aromatic ketones
    • Kumaraswamy G., and Ramesh S. Soaked Phaseolus aureus L: an efficient biocatalyst for asymmetric reduction of prochiral aromatic ketones. Green Chem. 5 (2003) 306-308
    • (2003) Green Chem. , vol.5 , pp. 306-308
    • Kumaraswamy, G.1    Ramesh, S.2
  • 8
    • 1142305981 scopus 로고    scopus 로고
    • Ability of different biomaterials to enantioselectively catalyze oxidation and reduction reactions
    • Nagaoka H. Ability of different biomaterials to enantioselectively catalyze oxidation and reduction reactions. Biotechnol. Prog. 20 (2004) 128-133
    • (2004) Biotechnol. Prog. , vol.20 , pp. 128-133
    • Nagaoka, H.1
  • 9
    • 0032530128 scopus 로고    scopus 로고
    • Highly stereoselective reduction of ketones by Geotrichum candidum
    • Nakamura K. Highly stereoselective reduction of ketones by Geotrichum candidum. J. Mol. Catal. B: Enzymatic 5 (1998) 129-132
    • (1998) J. Mol. Catal. B: Enzymatic , vol.5 , pp. 129-132
    • Nakamura, K.1
  • 10
    • 0029875971 scopus 로고    scopus 로고
    • Asymmetric reduction of ketones by the acetone powder of Geotrichum candidium
    • Nakamura K., Kitano K., Matsuda T., and Ohno A. Asymmetric reduction of ketones by the acetone powder of Geotrichum candidium. Tetrahedron Lett. 37 (1996) 1629-1632
    • (1996) Tetrahedron Lett. , vol.37 , pp. 1629-1632
    • Nakamura, K.1    Kitano, K.2    Matsuda, T.3    Ohno, A.4
  • 11
    • 0031766942 scopus 로고    scopus 로고
    • Asymmetric reduction of ketones by the acetone powder of Geotrichum candidum
    • Nakamura K., and Matsuda T. Asymmetric reduction of ketones by the acetone powder of Geotrichum candidum. J. Org. Chem. 63 (1998) 8957-8964
    • (1998) J. Org. Chem. , vol.63 , pp. 8957-8964
    • Nakamura, K.1    Matsuda, T.2
  • 12
    • 1842558913 scopus 로고    scopus 로고
    • Highly enantioselective conversion of racemic 1-phenyl-1, 2-ethanediol by stereoinversion involving a novel cofactor-dependent oxidoreduction system of Candida parapsilosis CCTCC M203011
    • Nie Y., Xu Y., and Mu X.Q. Highly enantioselective conversion of racemic 1-phenyl-1, 2-ethanediol by stereoinversion involving a novel cofactor-dependent oxidoreduction system of Candida parapsilosis CCTCC M203011. Org. Process. Res. Dev. 8 (2004) 246-251
    • (2004) Org. Process. Res. Dev. , vol.8 , pp. 246-251
    • Nie, Y.1    Xu, Y.2    Mu, X.Q.3
  • 13
    • 0001322847 scopus 로고    scopus 로고
    • General asymmetric hydrogenation of hetero-aromatic ketones
    • Ohkuma T., Koizumi M., Yoshida M., and Noyori R. General asymmetric hydrogenation of hetero-aromatic ketones. Org. Lett. 2 (2000) 1749-1751
    • (2000) Org. Lett. , vol.2 , pp. 1749-1751
    • Ohkuma, T.1    Koizumi, M.2    Yoshida, M.3    Noyori, R.4
  • 14
    • 0032963622 scopus 로고    scopus 로고
    • Acetophenone tolerance, chemical adaptation, and residual bioreductive capacity of non-fermenting baker's yeast (Saccharomyces cerevisiae) during sequential reactor cycles
    • Rogers R.S., Hackman J.R., Mercer V., and Delancey G.B. Acetophenone tolerance, chemical adaptation, and residual bioreductive capacity of non-fermenting baker's yeast (Saccharomyces cerevisiae) during sequential reactor cycles. J. Ind. Microbiol. Biotechnol. 22 (1999) 108-114
    • (1999) J. Ind. Microbiol. Biotechnol. , vol.22 , pp. 108-114
    • Rogers, R.S.1    Hackman, J.R.2    Mercer, V.3    Delancey, G.B.4
  • 16
    • 33748570459 scopus 로고    scopus 로고
    • Response surface optimization of the critical medium components for carbonyl reductase production by Candida viswanathii MTCC 5158
    • Soni P., Singh M., Kamble A.L., and Banerjee U.C. Response surface optimization of the critical medium components for carbonyl reductase production by Candida viswanathii MTCC 5158. Bioresource Technol. 98 (2007) 829-833
    • (2007) Bioresource Technol. , vol.98 , pp. 829-833
    • Soni, P.1    Singh, M.2    Kamble, A.L.3    Banerjee, U.C.4
  • 19
    • 34250201122 scopus 로고    scopus 로고
    • Aqueous-phase asymmetric transfer hydrogenation of ketones - a greener approach to chiral alcohols
    • Wu X.F., and Xiao J.L. Aqueous-phase asymmetric transfer hydrogenation of ketones - a greener approach to chiral alcohols. Chem. Commun. 24 (2007) 2449-2466
    • (2007) Chem. Commun. , vol.24 , pp. 2449-2466
    • Wu, X.F.1    Xiao, J.L.2
  • 20
    • 0037204732 scopus 로고    scopus 로고
    • Efficient enantioselective reduction of ketones with Daucus carota Root
    • Yadav J.S., Nanda S., Reddy P.T., and Rao A.B. Efficient enantioselective reduction of ketones with Daucus carota Root. J. Org. Chem. 67 (2002) 3900-3903
    • (2002) J. Org. Chem. , vol.67 , pp. 3900-3903
    • Yadav, J.S.1    Nanda, S.2    Reddy, P.T.3    Rao, A.B.4
  • 21
    • 0037148449 scopus 로고    scopus 로고
    • Stereoselective synthesis of (R)-(-)-denopamine, (R)-(-)-tembamide and (R)-(-)-aegeline via asymmetric reduction of azidoketones by Daucus carota in aqueous medium
    • Yadav J.S., Reddy P.T., Nanda S., and Rao A.B. Stereoselective synthesis of (R)-(-)-denopamine, (R)-(-)-tembamide and (R)-(-)-aegeline via asymmetric reduction of azidoketones by Daucus carota in aqueous medium. Tetrahedron: Asymmetry 12 (2001) 3381-3385
    • (2001) Tetrahedron: Asymmetry , vol.12 , pp. 3381-3385
    • Yadav, J.S.1    Reddy, P.T.2    Nanda, S.3    Rao, A.B.4
  • 22
    • 33746393199 scopus 로고    scopus 로고
    • Asymmetric reduction of ketones by employing Rhodotorula sp. AS2.2241 and synthesis of the β-blocker (R)-nifenalol
    • Yang W., Xu J.H., Xie Y., Zhao G., and Lin G.Q. Asymmetric reduction of ketones by employing Rhodotorula sp. AS2.2241 and synthesis of the β-blocker (R)-nifenalol. Tetrahedron: Asymmetry 17 (2006) 1769-1774
    • (2006) Tetrahedron: Asymmetry , vol.17 , pp. 1769-1774
    • Yang, W.1    Xu, J.H.2    Xie, Y.3    Zhao, G.4    Lin, G.Q.5
  • 23
    • 4644241379 scopus 로고    scopus 로고
    • Challenges in the development of an efficient enzymatic process in the pharmaceutical industry
    • Yazbeck D.R., Martinez C.A., Hu S.H., and Tao J.H. Challenges in the development of an efficient enzymatic process in the pharmaceutical industry. Tetrahedron: Asymmetry 15 (2004) 2757-2763
    • (2004) Tetrahedron: Asymmetry , vol.15 , pp. 2757-2763
    • Yazbeck, D.R.1    Martinez, C.A.2    Hu, S.H.3    Tao, J.H.4
  • 24
    • 26444620937 scopus 로고    scopus 로고
    • 'Green' synthesis of important pharmaceutical building blocks: enzymatic access to enantiomerically pure α-chloroalcohols
    • Zhu D., Chandrani M., and Hua L. 'Green' synthesis of important pharmaceutical building blocks: enzymatic access to enantiomerically pure α-chloroalcohols. Tetrahedron: Asymmetry 16 (2005) 3275-3278
    • (2005) Tetrahedron: Asymmetry , vol.16 , pp. 3275-3278
    • Zhu, D.1    Chandrani, M.2    Hua, L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.