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Volumn 18, Issue 11, 2013, Pages 13910-13919

The henry reaction in [Bmim][PF6]-based microemulsions promoted by acylase

Author keywords

Acylase; Enzyme promiscuity; Henry reaction; Water in Bmim PF6 microemulsion

Indexed keywords

ALDEHYDE; AMIDASE;

EID: 84888591071     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules181113910     Document Type: Article
Times cited : (12)

References (28)
  • 1
    • 84862098736 scopus 로고    scopus 로고
    • Biocatalytic Approaches to the Henry (Nitroaldol) Reaction
    • Milner, S.E.; Moody, T.S.; Maguire, A.R. Biocatalytic Approaches to the Henry (Nitroaldol) Reaction. Eur. J. Org. Chem. 2012, 2012, 3059-3067.
    • (2012) Eur. J. Org. Chem. , vol.2012 , pp. 3059-3067
    • Milner, S.E.1    Moody, T.S.2    Maguire, A.R.3
  • 2
    • 0033546386 scopus 로고    scopus 로고
    • P(RNCH2CH2)3N: An efficient promoter for the nitroaldol (Henry) reaction
    • Kisanga, P.B.; Verkade, J.G. P(RNCH2CH2)3N: An efficient promoter for the nitroaldol (Henry) reaction. J. Org. Chem. 1999, 64, 4298-4303.
    • (1999) J. Org. Chem. , vol.64 , pp. 4298-4303
    • Kisanga, P.B.1    Verkade, J.G.2
  • 6
    • 84876790465 scopus 로고    scopus 로고
    • Ethyl acrylate conjugated polystyryl-diphenylphosphine-An extremely efficient catalyst for Henry reaction under solvent-free conditions (SolFC)
    • Rokhum, L.; Bez, G. Ethyl acrylate conjugated polystyryl- diphenylphosphine-An extremely efficient catalyst for Henry reaction under solvent-free conditions (SolFC). Can. J. Chem. 2012, 91, 300-306.
    • (2012) Can. J. Chem. , vol.91 , pp. 300-306
    • Rokhum, L.1    Bez, G.2
  • 7
    • 1642264118 scopus 로고    scopus 로고
    • Hydrotalcite catalysis in ionic liquid medium: A recyclable reaction system for heterogeneous Knoevenagel and nitroaldol condensation
    • Khan, F.A.; Dash, J.; Satapathy, R.; Upadhyay, S.K. Hydrotalcite catalysis in ionic liquid medium: A recyclable reaction system for heterogeneous Knoevenagel and nitroaldol condensation. Tetrahedron Lett. 2004, 45, 3055-3058.
    • (2004) Tetrahedron Lett. , vol.45 , pp. 3055-3058
    • Khan, F.A.1    Dash, J.2    Satapathy, R.3    Upadhyay, S.K.4
  • 8
    • 0034603590 scopus 로고    scopus 로고
    • 1,5,7- Triazabicyclo[4.4.0]dec-1-ene (TBD), 7-methyl-TBD (MTBD) and the polymer-supported TBD (P-TBD): Three efficient catalysts for the nitroaldol (Henry) reaction and for the addition of dialkyl phosphites to unsaturated systems
    • Simoni, D.; Rondanin, R.; Morini, M.; Baruchello, R.; Invidiata, F.P. 1,5,7- Triazabicyclo[4.4.0]dec-1-ene (TBD), 7-methyl-TBD (MTBD) and the polymer-supported TBD (P-TBD): Three efficient catalysts for the nitroaldol (Henry) reaction and for the addition of dialkyl phosphites to unsaturated systems. Tetrahedron Lett. 2000, 41, 1607-1610.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 1607-1610
    • Simoni, D.1    Rondanin, R.2    Morini, M.3    Baruchello, R.4    Invidiata, F.P.5
  • 9
    • 84877713484 scopus 로고    scopus 로고
    • Henry reaction in aqueous media at neutral pH
    • Bora, P.P.; Bez, G. Henry reaction in aqueous media at neutral pH. Eur. J. Org. Chem. 2013, 2013, 2922-2929.
    • (2013) Eur. J. Org. Chem. , vol.2013 , pp. 2922-2929
    • Bora, P.P.1    Bez, G.2
  • 10
    • 73749083243 scopus 로고    scopus 로고
    • Hydrolase-catalyzed fast Henry reaction of nitroalkanes and aldehydes in organic media
    • Wang, J.-L.; Li, X.; Xie, H.-Y.; Liu, B.-K.; Lin, X.-F. Hydrolase-catalyzed fast Henry reaction of nitroalkanes and aldehydes in organic media. J. Biotechnol. 2010, 145, 240-243.
    • (2010) J. Biotechnol. , vol.145 , pp. 240-243
    • Wang, J.-L.1    Li, X.2    Xie, H.-Y.3    Liu, B.-K.4    Lin, X.-F.5
  • 11
    • 75649119278 scopus 로고    scopus 로고
    • TMEDA catalyzed Henry (nitroaldol) reaction under metal and solvent-free conditions
    • Majhi, A.; Kadam, S.T.; Kim, S.S. TMEDA catalyzed Henry (nitroaldol) reaction under metal and solvent-free conditions. Bull. Korean Chem. Soc. 2009, 30, 1767-1770.
    • (2009) Bull. Korean Chem. Soc. , vol.30 , pp. 1767-1770
    • Majhi, A.1    Kadam, S.T.2    Kim, S.S.3
  • 12
    • 0032558660 scopus 로고    scopus 로고
    • A one pot, solvent-free synthesis of acyclic a-nitro ketones through the nitroaldol reaction
    • Ballini, R.; Bosica, G.; Parrini, M. A one pot, solvent-free synthesis of acyclic a-nitro ketones through the nitroaldol reaction. Tetrahedron Lett. 1998, 39, 7963-7964.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 7963-7964
    • Ballini, R.1    Bosica, G.2    Parrini, M.3
  • 13
    • 33344458899 scopus 로고    scopus 로고
    • Rapid microwave-assisted henry reaction in solvent-free processes
    • Changsheng, R.M.-A.H.R.; Gan, X.C.; Lai, G.; Wang, Z. Rapid microwave-assisted henry reaction in solvent-free processes. Synlett 2006, 2006, 387-390.
    • (2006) Synlett , vol.2006 , pp. 387-390
    • Changsheng, R.M.-A.H.R.1    Gan, X.C.2    Lai, G.3    Wang, Z.4
  • 14
    • 40849085140 scopus 로고    scopus 로고
    • Enantioselective Henry reaction catalyzed by trianglamine-Cu (OAc)2 complex under solvent-free conditions
    • Tanaka, K.; Hachiken, S. Enantioselective Henry reaction catalyzed by trianglamine-Cu (OAc)2 complex under solvent-free conditions. Tetrahedron Lett. 2008, 49, 2533-2536.
    • (2008) Tetrahedron Lett. , vol.49 , pp. 2533-2536
    • Tanaka, K.1    Hachiken, S.2
  • 15
    • 34250349059 scopus 로고    scopus 로고
    • Zinc-proline complex: An efficient, reusable catalyst for direct nitroaldol reaction in aqueous media
    • Reddy, K.R.; Rajasekhar, C.V.; Krishna, G.G. Zinc-proline complex: An efficient, reusable catalyst for direct nitroaldol reaction in aqueous media. Synth. Commun. 2007, 37, 1971-1976.
    • (2007) Synth. Commun. , vol.37 , pp. 1971-1976
    • Reddy, K.R.1    Rajasekhar, C.V.2    Krishna, G.G.3
  • 16
    • 34648828937 scopus 로고    scopus 로고
    • Iodine catalysis in aqueous medium: An improved reaction system for Knoevenagel and Nitroaldol condensation
    • Ren, Y.; Cai, C. Iodine catalysis in aqueous medium: An improved reaction system for Knoevenagel and Nitroaldol condensation. Catalysis Lett. 2007, 118, 134-138.
    • (2007) Catalysis Lett. , vol.118 , pp. 134-138
    • Ren, Y.1    Cai, C.2
  • 18
    • 33746265821 scopus 로고    scopus 로고
    • A biocatalytic Henry reaction-The hydroxynitrile lyase from Hevea brasiliensis also catalyzes nitroaldol reactions
    • Purkarthofer, T.; Gruber, K.; Gruber-Khadjawi, M.; Waich, K.; Skranc, W.; Mink, D.; Griengl, H. A biocatalytic Henry reaction-The hydroxynitrile lyase from Hevea brasiliensis also catalyzes nitroaldol reactions. Angew. Chem. Int. Ed. 2006, 45, 3454-3456.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 3454-3456
    • Purkarthofer, T.1    Gruber, K.2    Gruber-Khadjawi, M.3    Waich, K.4    Skranc, W.5    Mink, D.6    Griengl, H.7
  • 22
    • 84858071530 scopus 로고    scopus 로고
    • Lipase promiscuity and its biochemical applications
    • Kapoor, M.; Gupta, M.N. Lipase promiscuity and its biochemical applications. Process Biochem. 2012, 47, 555-569.
    • (2012) Process Biochem. , vol.47 , pp. 555-569
    • Kapoor, M.1    Gupta, M.N.2
  • 24
    • 78649451089 scopus 로고    scopus 로고
    • A novel water-in-ionic liquid microemulsion and its interfacial effect on the activity of laccase
    • Xue, L.; Qiu, H.; Li, Y.; Lu, L.; Huang, X.; Qu, Y. A novel water-in-ionic liquid microemulsion and its interfacial effect on the activity of laccase. Colloids Surf. B 2011, 82, 432-437.
    • (2011) Colloids Surf. B , vol.82 , pp. 432-437
    • Xue, L.1    Qiu, H.2    Li, Y.3    Lu, L.4    Huang, X.5    Qu, Y.6
  • 25
    • 60849139418 scopus 로고    scopus 로고
    • Biocatalysis in water-in-ionic liquid microemulsions: A case study with horseradish peroxidase
    • Moniruzzaman, M.; Kamiya, N.; Goto, M. Biocatalysis in water-in-ionic liquid microemulsions: A case study with horseradish peroxidase. Langmuir 2008, 25, 977-982.
    • (2008) Langmuir , vol.25 , pp. 977-982
    • Moniruzzaman, M.1    Kamiya, N.2    Goto, M.3
  • 27
    • 84856117892 scopus 로고    scopus 로고
    • The catalytic efficiency of lipase in a novel water-in-[Bmim][PF6] microemulsion stabilized by both AOT and Triton X-100
    • Xue, L.; Li, Y.; Zou, F.; Lu, L.; Zhao, Y.; Huang, X.; Qu, Y. The catalytic efficiency of lipase in a novel water-in-[Bmim][PF6] microemulsion stabilized by both AOT and Triton X-100. Colloids Surf. B 2012, 92, 360-366.
    • (2012) Colloids Surf. B , vol.92 , pp. 360-366
    • Xue, L.1    Li, Y.2    Zou, F.3    Lu, L.4    Zhao, Y.5    Huang, X.6    Qu, Y.7
  • 28
    • 21644443080 scopus 로고    scopus 로고
    • TX-100/water/1- butyl-3-methylimidazolium hexafluorophosphate microemulsions
    • Gao, Y.; Han, S.; Han, B.; Li, G.; Shen, D.; Li, Z.; Du, J.; Hou, W.; Zhang, G. TX-100/water/1- butyl-3-methylimidazolium hexafluorophosphate microemulsions. Langmuir 2005, 21, 5681-5684.
    • (2005) Langmuir , vol.21 , pp. 5681-5684
    • Gao, Y.1    Han, S.2    Han, B.3    Li, G.4    Shen, D.5    Li, Z.6    Du, J.7    Hou, W.8    Zhang, G.9


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.