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Volumn 30, Issue 2, 2012, Pages 238-244

Biocatalytic Knoevenagel reaction using alkaline protease from Bacillus licheniformis

Author keywords

Alkaline protease; Biocatalysis; Knoevenagel condensation

Indexed keywords

ACETYLACETONE; ALKALINE PROTEASE; BACILLUS LICHENIFORMIS; BIOCATALYSIS; BIOCATALYTIC REACTION; ETHYLACETOACETATE; FUNCTIONALIZED; GOOD YIELD; KNOEVENAGEL CONDENSATION; KNOEVENAGEL REACTION; PRESENCE OF WATER; TRISUBSTITUTED ALKENES; UNSATURATED ALDEHYDES; UNSATURATED CARBONYL COMPOUNDS;

EID: 84863359869     PISSN: 10242422     EISSN: 10292446     Source Type: Journal    
DOI: 10.3109/10242422.2012.662961     Document Type: Article
Times cited : (25)

References (51)
  • 1
    • 34347246249 scopus 로고    scopus 로고
    • Rearrangement of propargylic esters: Metal-based stereospecific synthesis of (E)- and (Z)-knoevenagel derivatives
    • DOI 10.1021/ja072864r
    • Barluenga J, Riesgo L, Vicente R, Luis AL, Tomás M. 2007. Rearrangement of propargylic esters: metal-based stereospecifc synthesis of (e)-and (Z)-knoevenagel derivatives. J am Chem Soc 129:7772-7773. (Pubitemid 46998173)
    • (2007) Journal of the American Chemical Society , vol.129 , Issue.25 , pp. 7772-7773
    • Barluenga, J.1    Riesgo, L.2    Vicente, R.3    Lopez, L.A.4    Tomas, M.5
  • 2
    • 40849116176 scopus 로고    scopus 로고
    • Magnesium perchlorate as eff-cient lewis acid for the knoevenagel condensation between b-diketones and aldehydes
    • Bartoli G, Bosco M, Carlone A, Dalpozzo R, galzerano P, Melchiorre P, Sambri L. 2008. Magnesium perchlorate as eff-cient Lewis acid for the Knoevenagel condensation between b-diketones and aldehydes. Tetrahedron Lett 49:2555-2557.
    • (2008) Tetrahedron Lett , vol.49 , pp. 2555-2557
    • Bartoli, G.1    Bosco, M.2    Carlone, A.3    Dalpozzo, R.4    Galzerano, P.5    Melchiorre, P.6    Sambri, L.7
  • 3
    • 10044248344 scopus 로고    scopus 로고
    • Catalytic promiscuity in biocatalysis: Using old enzymes to form new bonds and follow new pathways
    • DOI 10.1002/anie.200460416
    • Bornscheuer UT, Kazlauskas RJ. 2004. Catalytic promiscuity in biocatalysis: using old enzymes to form new bonds and follow new pathways. angew Chem int ed 43:6032-6040. (Pubitemid 39611872)
    • (2004) Angewandte Chemie - International Edition , vol.43 , Issue.45 , pp. 6032-6040
    • Bornscheuer, U.T.1    Kazlauskas, R.J.2
  • 4
    • 77958046500 scopus 로고    scopus 로고
    • Hydrolases: Cata-lytically promiscuous enzymes for non-conventional reactions in organic synthesis
    • Busto E, Gotor-Fernández V, Gotor V. 2010. Hydrolases: cata-lytically promiscuous enzymes for non-conventional reactions in organic synthesis. Chem Soc Rev 39:4504-4523.
    • (2010) Chem Soc Rev , vol.39 , pp. 4504-4523
    • Busto, E.1    Gotor-Fernández, V.2    Gotor, V.3
  • 5
    • 33845469112 scopus 로고
    • Knoevenagel condensation in the heterogeneous phase using aluminum phosphate-aluminum oxide as a new catalyst
    • Cabello JA, Campelo JM, Garcia A, Luna D, Marinas JM. 1984. Knoevenagel condensation in the heterogeneous phase using aluminum phosphate-aluminum oxide as a new catalyst. J org Chem 49:5195-5197.
    • (1984) J Org Chem , vol.49 , pp. 5195-5197
    • Cabello, J.A.1    Campelo, J.M.2    Garcia, A.3    Luna, D.4    Marinas, J.M.5
  • 6
    • 78651397152 scopus 로고    scopus 로고
    • The lipase-catalyzed asymmetric C-C michael addition
    • Cai JF, Guan Z, He YH. 2011. The lipase-catalyzed asymmetric C-C Michael addition. J Mol Catal B enzym 68:240-244.
    • (2011) J Mol Catal B Enzym , vol.68 , pp. 240-244
    • Cai, J.F.1    Guan, Z.2    He, Y.H.3
  • 7
    • 78649334393 scopus 로고    scopus 로고
    • A tandem aldol condensation/dehydration co-catalyzed by acylase and n-heterocy-clic compounds in organic media
    • Chen X, Liu BK, Kang H, Lin XF. 2011. A tandem aldol condensation/ dehydration co-catalyzed by acylase and n-heterocy-clic compounds in organic media. J Mol Catal B enzym 68: 71-76.
    • (2011) J Mol Catal B Enzym , vol.68 , pp. 71-76
    • Chen, X.1    Liu, B.K.2    Kang, H.3    Lin, X.F.4
  • 8
    • 84863379195 scopus 로고    scopus 로고
    • Synthesis of 4-Thienyl substituted dihy-dropyridines derivatives
    • Deng L, Xu MX. 2002. Synthesis of 4-thienyl substituted dihy-dropyridines derivatives. Huaxi Yaoxue Zazhi 1:37-38.
    • (2002) Huaxi Yaoxue Zazhi , vol.1 , pp. 37-38
    • Deng, L.1    Xu, M.X.2
  • 9
    • 77955422225 scopus 로고    scopus 로고
    • Promiscuous candida antarctica lipase b-catalyzed synthesis of b-amino esters via aza-michael addition of amines to acrylates
    • Dhake KP, Tambade PJ, Singhal RS, Bhanage BM. 2010. Promiscuous Candida antarctica lipase B-catalyzed synthesis of b-amino esters via aza-Michael addition of amines to acrylates. Tetrahedron Lett 51:4455-4458.
    • (2010) Tetrahedron Lett , vol.51 , pp. 4455-4458
    • Dhake, K.P.1    Tambade, P.J.2    Singhal, R.S.3    Bhanage, B.M.4
  • 10
    • 79955634803 scopus 로고    scopus 로고
    • Lipase CaL-B does not catalyze a promiscuous decarboxylative aldol addition or Knoevenagel reaction
    • Evitt AS, Bornscheuer UT. 2011. Lipase CaL-B does not catalyze a promiscuous decarboxylative aldol addition or Knoevenagel reaction. green Chem 13:1141-1142.
    • (2011) Green Chem , vol.13 , pp. 1141-1142
    • Evitt, A.S.1    Bornscheuer, U.T.2
  • 11
    • 0042970210 scopus 로고    scopus 로고
    • Role of water activity on the synthesis of vinyl thymidine catalyzed by protease from Bacillus subtilis
    • DOI 10.1002/mabi.200350012
    • Fan H, Kitagawa M, Rakub T, Tokiwa Y. 2003. Role of water activity on the synthesis of vinyl thymidine catalyzed by protease from Bacillus Subtilis. Macromol Biosci 3:420-424. (Pubitemid 37010636)
    • (2003) Macromolecular Bioscience , vol.3 , Issue.8 , pp. 420-424
    • Fan, H.1    Kitagawa, M.2    Raku, T.3    Tokiwa, Y.4
  • 12
    • 71549120756 scopus 로고    scopus 로고
    • Lipase-catalysed decarboxylative aldol reaction and decarboxy-lative Knoevenagel reaction
    • Feng XW, Li C, Wang N, Li K, Zhang WW, Wang Z, Yu XQ. 2009. Lipase-catalysed decarboxylative aldol reaction and decarboxy-lative Knoevenagel reaction. green Chem 11:1933-1936.
    • (2009) Green Chem , vol.11 , pp. 1933-1936
    • Feng, X.W.1    Li, C.2    Wang, N.3    Li, K.4    Zhang, W.W.5    Wang, Z.6    Yu, X.Q.7
  • 14
    • 79955766024 scopus 로고    scopus 로고
    • Synthesis of (R)-b-nitro alcohols catalyzed by r-selective hydroxynitrile lyase from arabidopsis thaliana in the aqueous-organic biphasic system
    • Fuhshuku K, Asano Y. 2011. Synthesis of (R)-b-nitro alcohols catalyzed by R-selective hydroxynitrile lyase from Arabidopsis thaliana in the aqueous-organic biphasic system. J Biotechnol 153:153-159.
    • (2011) J Biotechnol , vol.153 , pp. 153-159
    • Fuhshuku, K.1    Asano, Y.2
  • 15
    • 79955550633 scopus 로고    scopus 로고
    • A novel light induced knoevenagel condensation of meldrum's acid with aromatic aldehydes in aqueous ethanol
    • Ghosh S, Das J, Chattopadhyay S. 2011. a novel light induced Knoevenagel condensation of Meldrum's acid with aromatic aldehydes in aqueous ethanol. Tetrahedron Lett 52:2869-2872.
    • (2011) Tetrahedron Lett , vol.52 , pp. 2869-2872
    • Ghosh, S.1    Das, J.2    Chattopadhyay, S.3
  • 17
    • 77949391402 scopus 로고    scopus 로고
    • L-arginine as a cost-effective and recyclable catalyst for the synthesis of a,b-unsaturated nitriles and ketones in an ionic liquid
    • Hu Y, Guan Z, He YH, Louwagie N, Yao MJ. 2010a. L-arginine as a cost-effective and recyclable catalyst for the synthesis of a,b-unsaturated nitriles and ketones in an ionic liquid. J Chem Res 34:22-24.
    • (2010) J Chem Res , vol.34 , pp. 22-24
    • Hu, Y.1    Guan, Z.2    He, Y.H.3    Louwagie, N.4    Yao, M.J.5
  • 18
    • 76749149512 scopus 로고    scopus 로고
    • A simple method for the preparation of functionalized trisubstituted alkenes and a,b,g,d-unsatu-rated carbonyl compounds by using natural amino acid l-tryptophan
    • Hu Y, He YH, Guan Z. 2010b. a simple method for the preparation of functionalized trisubstituted alkenes and a,b,g,d-unsatu-rated carbonyl compounds by using natural amino acid l-tryptophan. Catal Commun 11:656-659.
    • (2010) Catal Commun , vol.11 , pp. 656-659
    • Hu, Y.1    He, Y.H.2    Guan, Z.3
  • 19
    • 79959757238 scopus 로고    scopus 로고
    • Biocatalytic promiscuity
    • Humble MS, Berglund P. 2011. Biocatalytic promiscuity. eur J org Chem 2011:3391-3401.
    • (2011) Eur J Org Chem , vol.2011 , pp. 3391-3401
    • Humble, M.S.1    Berglund, P.2
  • 21
    • 79958288624 scopus 로고    scopus 로고
    • Nickel nanoparticles catalyzed chem-oselective knoevenagel condensation of meldrum's acid and tandem enol lactonizations via cascade cyclization sequence
    • Khurana JM, Vij K. 2011. nickel nanoparticles catalyzed chem-oselective Knoevenagel condensation of Meldrum's acid and tandem enol lactonizations via cascade cyclization sequence. Tetrahedron Lett 52:3666-3669.
    • (2011) Tetrahedron Lett , vol.52 , pp. 3666-3669
    • Khurana, J.M.1    Vij, K.2
  • 22
    • 38149041619 scopus 로고    scopus 로고
    • Understanding promiscuous amidase activity of an esterase from Bacillus subtilis
    • Kourist R, Bartsch S, Fransson L, Hult K, Bornscheuer uT. 2008. understanding promiscuous amidase activity of an esterase from Bacillus subtilis. ChemBioChem 9:67-69.
    • (2008) ChemBioChem , vol.9 , pp. 67-69
    • Kourist, R.1    Bartsch, S.2    Fransson, L.3    Hult, K.4    Bornscheuer, U.T.5
  • 23
    • 0024653016 scopus 로고
    • Enzymatic catalysis in anhydrous organic solvents
    • Klibanov AM. 1989. enzymatic catalysis in anhydrous organic solvents. Trends Biochem Sci 14:141-144.
    • (1989) Trends Biochem Sci , vol.14 , pp. 141-144
    • Klibanov, A.M.1
  • 24
    • 78049372110 scopus 로고    scopus 로고
    • Lipase-catalysed tandem Knoevenagel condensation and esterifcation with alcohol cosolvents
    • Lai YF, Zheng H, Chai SJ, Zhang PF, Chen XZ. 2010. Lipase-catalysed tandem Knoevenagel condensation and esterifcation with alcohol cosolvents. green Chem 12:1917-1918.
    • (2010) Green Chem , vol.12 , pp. 1917-1918
    • Lai, Y.F.1    Zheng, H.2    Chai, S.J.3    Zhang, P.F.4    Chen, X.Z.5
  • 25
    • 0001541455 scopus 로고
    • 4/THF/pyridin(i). alkyliden-und aryli-denmalonester bei 0-25°C
    • 4/THF/pyridin(i). alkyliden-und aryli-denmalonester bei 0-25°C. Tetrahedron Lett 11:4723-4724.
    • (1970) Tetrahedron Lett , vol.11 , pp. 4723-4724
    • Lehnert, W.1
  • 26
    • 38149122142 scopus 로고    scopus 로고
    • Catalytic promiscuity in the a/b-hydrolase superfamily: Hydroxamic acid formation, C-C bond formation, ester and thioester hydrolysis in the C-C hydrolase family
    • Li C, Hassler M, Bugg TDH. 2008. Catalytic promiscuity in the a/b-hydrolase superfamily: hydroxamic acid formation, C-C bond formation, ester and thioester hydrolysis in the C-C hydrolase family. ChemBioChem 9:71-76.
    • (2008) ChemBioChem , vol.9 , pp. 71-76
    • Li, C.1    Hassler, M.2    Bugg, T.D.H.3
  • 27
    • 78649447899 scopus 로고    scopus 로고
    • Promiscuous protease-catalyzed aldol reactions: A facile biocatalytic protocol for carbon-carbon bond formation in aqueous media
    • Li C, Zhou YJ, Wang N, Feng XW, Li K, Yu XQ. 2010a. Promiscuous protease-catalyzed aldol reactions: a facile biocatalytic protocol for carbon-carbon bond formation in aqueous media. J Biotechnol 150:539-545.
    • (2010) J Biotechnol , vol.150 , pp. 539-545
    • Li, C.1    Zhou, Y.J.2    Wang, N.3    Feng, X.W.4    Li, K.5    Yu, X.Q.6
  • 28
    • 78651310908 scopus 로고    scopus 로고
    • Nuclease p1: A new bio-catalyst for direct asymmetric aldol reaction under solvent-free conditions
    • Li HH, He YH, Yuan Y, Guan Z. 2011. nuclease p1: a new bio-catalyst for direct asymmetric aldol reaction under solvent-free conditions. green Chem 13:185-189.
    • (2011) Green Chem , vol.13 , pp. 185-189
    • Li, H.H.1    He, Y.H.2    Yuan, Y.3    Guan, Z.4
  • 29
    • 77956053152 scopus 로고    scopus 로고
    • Orga-nocatalytic asymmetric inverse-electron-demand Diels-alder reaction of electron-defcient dienes and crotonaldehyde
    • Li JL, Kang TR, Zhou SL, Li R, Wu L, Chen YC. 2010b. orga-nocatalytic asymmetric inverse-electron-demand Diels-alder reaction of electron-defcient dienes and crotonaldehyde. angew Chem int ed 49:6418-6420.
    • (2010) Angew Chem Int Ed , vol.49 , pp. 6418-6420
    • Li, J.L.1    Kang, T.R.2    Zhou, S.L.3    Li, R.4    Wu, L.5    Chen, Y.C.6
  • 30
    • 80052806973 scopus 로고    scopus 로고
    • Use of protease from Bacillus licheniformis as promiscuous catalyst for organic synthesis: Applications in C-C and C-n bond formation reactions
    • López-Iglesias M, Busto E, Gotor V, Gotor-Fernández V. 2011. use of protease from Bacillus licheniformis as promiscuous catalyst for organic synthesis: applications in C-C and C-n bond formation reactions. adv Synth Catal 353:2345-2353.
    • (2011) Adv Synth Catal , vol.353 , pp. 2345-2353
    • López-Iglesias, M.1    Busto, E.2    Gotor, V.3    Gotor-Fernández, V.4
  • 31
    • 33646449394 scopus 로고    scopus 로고
    • Carbon-Carbon bond forming solid-Phase reactions
    • Lorsbach BA, Kurth MJ. 1999. Carbon-carbon bond forming solid-phase reactions. Chem Rev 99:1549-1582.
    • (1999) Chem Rev , vol.99 , pp. 1549-1582
    • Lorsbach, B.A.1    Kurth, M.J.2
  • 32
    • 67349257142 scopus 로고    scopus 로고
    • Controllable enzymatic markovnikov addition and acylation of thiols to vinyl esters
    • Lou FW, Liu BK, Wang JL, Pan Q, Lin XF 2009. Controllable enzymatic Markovnikov addition and acylation of thiols to vinyl esters. J Mol Catal B enzym 60:64-68.
    • (2009) J Mol Catal B Enzym , vol.60 , pp. 64-68
    • Lou, F.W.1    Liu, B.K.2    Wang, J.L.3    Pan, Q.4    Lin, X.F.5
  • 33
    • 0024385914 scopus 로고
    • Tyrphostins inhibit epidermal growth factor (EGF)-receptor tyrosine kinase activity in living cells and EGF-stimulated cell proliferation
    • Lyall R, Zilberstein A, Gazit A, Gilon C, Levitzki A, Schlessinger J. 1989. Tyrphostins inhibit epidermal growth factor (egF)-receptor tyrosine kinase activity in living cells and egF-stimulated cell proliferation. J Biol Chem 2649:14503-14509. (Pubitemid 19214287)
    • (1989) Journal of Biological Chemistry , vol.264 , Issue.24 , pp. 14503-14509
    • Lyall, R.M.1    Zilberstein, A.2    Gazit, A.3    Gilon, C.4    Levitzki, A.5    Schlessinger, J.6
  • 34
    • 78049495036 scopus 로고    scopus 로고
    • Importance of the nature of a-substituents in pyrrolidine organocatalysts in asymmetric michael additions
    • Mahendra PP, Akhilesh KS, Raghavan BS. 2010. importance of the nature of a-substituents in pyrrolidine organocatalysts in asymmetric michael additions. J org Chem 75:7310-7321.
    • (2010) J Org Chem , vol.75 , pp. 7310-7321
    • Mahendra, P.P.1    Akhilesh, K.S.2    Raghavan, B.S.3
  • 35
    • 37049066839 scopus 로고
    • Cheminform abstract: Cadmium iodide as a new catalyst for knoevenagel condensations
    • Prajapati D, Sandhu JS. 1993. Cheminform abstract: cadmium iodide as a new catalyst for knoevenagel condensations. J Chem Soc Perkin Trans 1:739-740.
    • (1993) J Chem Soc Perkin Trans , vol.1 , pp. 739-740
    • Prajapati, D.1    Sandhu, J.S.2
  • 37
    • 0025951196 scopus 로고
    • Zinc chloride as a new catalyst for knoevenagel condensation
    • Rao PS, Venkataratnam RV. 1991. Zinc chloride as a new catalyst for knoevenagel condensation. Tetrahedron Lett 32:5821-5822.
    • (1991) Tetrahedron Lett , vol.32 , pp. 5821-5822
    • Rao, P.S.1    Venkataratnam, R.V.2
  • 38
    • 0031562446 scopus 로고    scopus 로고
    • Rare-earth (RE) exchanged NaY zeolite promoted Knoevenagel condensation
    • DOI 10.1016/S0040-4039(97)00180-9, PII S0040403997001809
    • Reddy TI, Varma RS. 1997. Rare-earth (Re) exchanged naY zeolite promoted knoevenagel condensation. Tetrahedron Lett 38:1721-1724. (Pubitemid 27102313)
    • (1997) Tetrahedron Letters , vol.38 , Issue.10 , pp. 1721-1724
    • Reddy, T.I.1    Varma, R.S.2
  • 39
    • 78649829673 scopus 로고    scopus 로고
    • Silica-immobilized piperazine: A sustainable organocatalyst for aldol and knoevenagel reactions
    • Shanmuganathan S, Greiner L, Domínguez de María P. 2010. Silica-immobilized piperazine: a sustainable organocatalyst for aldol and Knoevenagel reactions. Tetrahedron Lett 51:6670-6672.
    • (2010) Tetrahedron Lett , vol.51 , pp. 6670-6672
    • Shanmuganathan, S.1    Greiner, L.2    Domínguez De María, P.3
  • 40
    • 0024520721 scopus 로고
    • Specific inhibitors of tyrosine-specific protein kinases: Properties of 4-hydroxycinnamamide derivatives in vitro
    • Shiraishi T, Owada MK, Tatsuki M, Yamashita Y, Kaun-Aga T. 1989. Specifc inhibitors of tyrosine-specifc protein kinases: properties of 4-hydroxycinnamamide derivatives in Vitro. Cancer Res 49:2374-2378. (Pubitemid 19125564)
    • (1989) Cancer Research , vol.49 , Issue.9 , pp. 2374-2378
    • Shiraishi, T.1    Koji Owada, M.2    Tatsuka, M.3    Yamashita, T.4    Watanabe, K.5    Kakunaga, T.6
  • 41
    • 77950259989 scopus 로고    scopus 로고
    • Synthesis of diphenylamine-based novel fuores-cent styryl colorants by Knoevenagel condensation using a conventional method, biocatalyst, and deep eutectic solvent
    • Sonawane YA, Phadtare SB, Borse BN, Jagtap amit R, Shankar-Ling GS. 2010. Synthesis of diphenylamine-based novel fuores-cent styryl colorants by Knoevenagel condensation using a conventional method, biocatalyst, and deep eutectic solvent. org Lett 12:1456-1459.
    • (2010) Org Lett , vol.12 , pp. 1456-1459
    • Sonawane, Y.A.1    Phadtare, S.B.2    Borse, B.N.3    Jagtap Amit, R.4    Shankar-Ling, G.S.5
  • 42
    • 0001274945 scopus 로고
    • Knoevenagel condensation catalysed by aluminium oxide
    • Texier-Boullet F, Foucaud A. 1982. Knoevenagel condensation catalysed by aluminium oxide. Tetrahedron Lett 23:4927-4928.
    • (1982) Tetrahedron Lett , vol.23 , pp. 4927-4928
    • Texier-Boullet, F.1    Foucaud, A.2
  • 44
    • 80051591376 scopus 로고    scopus 로고
    • Biocatalytic domino reaction: Synthesis of 2H-1-benzopyran-2-one derivatives using alkaline protease from Bacillus licheniformis
    • Wang CH, Guan Z, He YH. 2011. Biocatalytic domino reaction: synthesis of 2H-1-benzopyran-2-one derivatives using alkaline protease from Bacillus licheniformis. green Chem 13:2048-2054.
    • (2011) Green Chem , vol.13 , pp. 2048-2054
    • Wang, C.H.1    Guan, Z.2    He, Y.H.3
  • 45
    • 73749083243 scopus 로고    scopus 로고
    • Hydrolase-catalyzed fast henry reaction of nitroalkanes and aldehydes in organic media
    • Wang JL, Li X, Xie HY, Liu BK, Lin XF. 2010a. Hydrolase-catalyzed fast Henry reaction of nitroalkanes and aldehydes in organic media. J Biotechnol 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
  • 46
    • 77956899695 scopus 로고    scopus 로고
    • Enzyme-mediated domino synthesis of 2-Alkylbenzimidazoles in solvent-free system: A green route to heterocyclic compound
    • Wang L, Li C, Wang N, Li K, Chen X, Yu XQ. 2010b. enzyme-mediated domino synthesis of 2-alkylbenzimidazoles in solvent-free system: a green route to heterocyclic compound. J Mol Catal B enzym 67:16-20.
    • (2010) J Mol Catal B Enzym , vol.67 , pp. 16-20
    • Wang, L.1    Li, C.2    Wang, N.3    Li, K.4    Chen, X.5    Yu, X.Q.6
  • 47
    • 77958009739 scopus 로고    scopus 로고
    • Enzymatic promiscuity for organic synthesis and cascade process
    • Wu Q, Liu BK, Lin XF. 2010. enzymatic promiscuity for organic synthesis and cascade process. Curr org Chem 14:1966-1988.
    • (2010) Curr Org Chem , vol.14 , pp. 1966-1988
    • Wu, Q.1    Liu, B.K.2    Lin, X.F.3
  • 48
    • 33845931812 scopus 로고    scopus 로고
    • Efficient Knoevenagel condensation catalyzed by cyclic guanidinium lactate ionic liquid as medium
    • DOI 10.1016/j.catcom.2006.05.034, PII S1566736706001749
    • Xin X, Guo X, Duan HF, Lin YJ, Sun H. 2007. effcient Kno-evenagel condensation catalyzed by cyclic guanidinium lactate ionic liquid as medium. Catal Commun 8:115-117. (Pubitemid 46038831)
    • (2007) Catalysis Communications , vol.8 , Issue.2 , pp. 115-117
    • Xin, X.1    Guo, X.2    Duan, H.3    Lin, Y.4    Sun, H.5
  • 49
    • 34250717461 scopus 로고    scopus 로고
    • Promiscuous zinc-dependent acylase-mediated carbon-carbon bond formation in organic media
    • DOI 10.1039/b700327g
    • Xu JM, Zhang F, Liu BK, Wu Q, Lin XF. 2007. Promiscuous zinc-dependent acylase-mediated carbon-carbon bond formation in organic media. Chem Commun 2007:2078-2080. (Pubitemid 46959484)
    • (2007) Chemical Communications , Issue.20 , pp. 2078-2080
    • Xu, J.-M.1    Zhang, F.2    Liu, B.-K.3    Wu, Q.4    Lin, X.-F.5
  • 50
    • 79958001632 scopus 로고    scopus 로고
    • Acidic proteinase from Aspergillus usamii catalyzed Michael addition of ketones to nitroolefns
    • Xu KL, Guan Z, He YH. 2011. acidic proteinase from Aspergillus usamii catalyzed Michael addition of ketones to nitroolefns. J Mol Catal B enzym 71:108-112.
    • (2011) J Mol Catal B Enzym , vol.71 , pp. 108-112
    • Xu, K.L.1    Guan, Z.2    He, Y.H.3
  • 51
    • 63749085583 scopus 로고    scopus 로고
    • 5 catalyzed condensation of 1,3-dicarbonyl compounds and aldehydes: A facile synthesis of trisubstituted alkenes
    • 5 catalyzed condensation of 1,3-dicarbonyl compounds and aldehydes: a facile synthesis of trisubstituted alkenes. Tetrahedron Lett 50:2470-2473.
    • (2009) Tetrahedron Lett , vol.50 , pp. 2470-2473
    • Yadav, J.S.1    Bhunia, D.C.2    Singh, V.K.3    Srihari, P.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.