메뉴 건너뛰기




Volumn 17, Issue 6, 2015, Pages 736-742

Stereoselective Bioreduction of α-Azido Ketones by Whole Cells of Marine-Derived Fungi

Author keywords

Azido alcohols; Biocatalysis; Biotransformation; Marine fungi; Mycelia

Indexed keywords

CATALYSIS; KETONES; NITROGEN COMPOUNDS;

EID: 84946498362     PISSN: 14362228     EISSN: 14362236     Source Type: Journal    
DOI: 10.1007/s10126-015-9644-x     Document Type: Article
Times cited : (21)

References (32)
  • 1
    • 50149097958 scopus 로고    scopus 로고
    • Synthesis of optically pure 2-azido-1-arylethanols with isolated enzymes and conversion to triazole-containing β-blocker analogues employing click chemistry
    • COI: 1:CAS:528:DC%2BD1cXosFKltrg%3D, PID: 18630881
    • Ankati H, Yang Y, Zhu D, Biehl ER, Hua L (2008) Synthesis of optically pure 2-azido-1-arylethanols with isolated enzymes and conversion to triazole-containing β-blocker analogues employing click chemistry. J Org Chem 73:6433–6436
    • (2008) J Org Chem , vol.73 , pp. 6433-6436
    • Ankati, H.1    Yang, Y.2    Zhu, D.3    Biehl, E.R.4    Hua, L.5
  • 2
    • 27844612307 scopus 로고    scopus 로고
    • Extreme environments as a resource for microorganisms and novel biocatalysts
    • COI: 1:CAS:528:DC%2BD2MXhtlamsr%2FN
    • Antranikian G, Vorgias CE, Bertoldo C (2005) Extreme environments as a resource for microorganisms and novel biocatalysts. Adv Biochem Eng Biotech 96:219–262
    • (2005) Adv Biochem Eng Biotech , vol.96 , pp. 219-262
    • Antranikian, G.1    Vorgias, C.E.2    Bertoldo, C.3
  • 3
    • 0027941227 scopus 로고
    • Chemoenzymatic synthesisof chiral β-azidoalcohols. Application to the preparation of chiral aziridines and aminoalcohols
    • Besse P, Veschambre H, Chênevert R, Dickman M (1994) Chemoenzymatic synthesisof chiral β-azidoalcohols. Application to the preparation of chiral aziridines and aminoalcohols. Tetrahedron-Asymmetry 5:1727–1744
    • (1994) Tetrahedron-Asymmetry , vol.5 , pp. 1727-1744
    • Besse, P.1    Veschambre, H.2    Chênevert, R.3    Dickman, M.4
  • 4
    • 64349114873 scopus 로고    scopus 로고
    • Tandem concurrent processes: one-pot single-catalyst biohydrogen transfer for the simultaneous preparation of enantiopure secondary alcohols
    • COI: 1:CAS:528:DC%2BD1MXksVylsA%3D%3D, PID: 19138072
    • Bisogno FR, Lavandera I, Kroutil W, Gotor V (2009) Tandem concurrent processes: one-pot single-catalyst biohydrogen transfer for the simultaneous preparation of enantiopure secondary alcohols. J Org Chem 74:1730–1732
    • (2009) J Org Chem , vol.74 , pp. 1730-1732
    • Bisogno, F.R.1    Lavandera, I.2    Kroutil, W.3    Gotor, V.4
  • 5
    • 0038824608 scopus 로고    scopus 로고
    • Stereoselective acylations of 1,2-azidoalcohols with vinyl acetate, catalyzed by lipase Amano OS
    • COI: 1:CAS:528:DC%2BD3sXksFGmsLk%3D
    • Brenelli ECS, Fernandes JLN (2003) Stereoselective acylations of 1,2-azidoalcohols with vinyl acetate, catalyzed by lipase Amano OS. Tetrahedron-Asymmetry 14:1255–1259
    • (2003) Tetrahedron-Asymmetry , vol.14 , pp. 1255-1259
    • Brenelli, E.C.S.1    Fernandes, J.L.N.2
  • 6
    • 1342311386 scopus 로고    scopus 로고
    • Marine-derived fungi: a chemically and biologically diverse group of microorganisms
    • COI: 1:CAS:528:DC%2BD2cXisFWgtb8%3D, PID: 15039840
    • Bugni TS, Ireland CM (2004) Marine-derived fungi: a chemically and biologically diverse group of microorganisms. Nat Prod Rep 21:143–163
    • (2004) Nat Prod Rep , vol.21 , pp. 143-163
    • Bugni, T.S.1    Ireland, C.M.2
  • 7
    • 58449093511 scopus 로고    scopus 로고
    • Biodiversity and biotechnological potential of mangrove-associated fungi
    • COI: 1:CAS:528:DC%2BD1MXisFChs7c%3D
    • Cheng Z, Pan J, Tang W, Chen Q, Lin Y (2009) Biodiversity and biotechnological potential of mangrove-associated fungi. J For Res 20:63–72
    • (2009) J For Res , vol.20 , pp. 63-72
    • Cheng, Z.1    Pan, J.2    Tang, W.3    Chen, Q.4    Lin, Y.5
  • 9
    • 33646010935 scopus 로고    scopus 로고
    • Bioreduction of 2-azido-1-arylethanones mediated by Geotrichum candidum and Rhodotorula glutinis
    • COI: 1:CAS:528:DC%2BD28Xjs1Khtrw%3D
    • Fardelone LC, Rodrigues JAR, Moran PJS (2006) Bioreduction of 2-azido-1-arylethanones mediated by Geotrichum candidum and Rhodotorula glutinis. J Mol Catal B Enzym 39:9–12
    • (2006) J Mol Catal B Enzym , vol.39 , pp. 9-12
    • Fardelone, L.C.1    Rodrigues, J.A.R.2    Moran, P.J.S.3
  • 10
    • 24944546402 scopus 로고    scopus 로고
    • Biotechnology - a sustainable alternative for chemical industry
    • Gavrilescua M, Chisti Y (2005) Biotechnology - a sustainable alternative for chemical industry. Biotechnol Adv 23:471–499
    • (2005) Biotechnol Adv , vol.23 , pp. 471-499
    • Gavrilescua, M.1    Chisti, Y.2
  • 13
    • 9944226680 scopus 로고    scopus 로고
    • Chemoenzymatic synthesis of (R)- and (S)-tembamide, aegeline and denopamine by a one-pot lipase resolution protocol
    • COI: 1:CAS:528:DC%2BD2cXhtVKrsLzE
    • Kamal A, Shaik AA, Sandbhor M, Malik MS (2004b) Chemoenzymatic synthesis of (R)- and (S)-tembamide, aegeline and denopamine by a one-pot lipase resolution protocol. Tetrahedron-Asymmetry 15:3939–3944
    • (2004) Tetrahedron-Asymmetry , vol.15 , pp. 3939-3944
    • Kamal, A.1    Shaik, A.A.2    Sandbhor, M.3    Malik, M.S.4
  • 14
    • 11044220079 scopus 로고    scopus 로고
    • Enzymes from higher eukaryotes for industrial biocatalysis
    • COI: 1:CAS:528:DC%2BD2MXhsV2hsLY%3D
    • Liu Z, Weis R, Gliede A (2004) Enzymes from higher eukaryotes for industrial biocatalysis. Food Technol Biotechnol 42:237–249
    • (2004) Food Technol Biotechnol , vol.42 , pp. 237-249
    • Liu, Z.1    Weis, R.2    Gliede, A.3
  • 16
    • 65349190562 scopus 로고    scopus 로고
    • Recent progress in biocatalysis for asymmetric oxidation and reduction
    • COI: 1:CAS:528:DC%2BD1MXltl2ksr4%3D
    • Matsuda T, Yamanaka R, Nakamura K (2009) Recent progress in biocatalysis for asymmetric oxidation and reduction. Tetrahedron-Asymmetry 20:513–557
    • (2009) Tetrahedron-Asymmetry , vol.20 , pp. 513-557
    • Matsuda, T.1    Yamanaka, R.2    Nakamura, K.3
  • 17
    • 84878839188 scopus 로고    scopus 로고
    • Non-enzymatic kinetic resolution of 1,2-azidoalcohols using a planar-chiral DMAP derivative catalyst
    • Mesas-Sánchez L, Díaz-Álvarez AE, Dinér P (2013) Non-enzymatic kinetic resolution of 1,2-azidoalcohols using a planar-chiral DMAP derivative catalyst. Tetrahedron 69:753–757
    • (2013) Tetrahedron , vol.69 , pp. 753-757
    • Mesas-Sánchez, L.1    Díaz-Álvarez, A.E.2    Dinér, P.3
  • 18
    • 4344650390 scopus 로고    scopus 로고
    • Marine natural products and related compounds in clinical and advanced preclinical trials
    • COI: 1:CAS:528:DC%2BD2cXkslWhtbo%3D, PID: 15332835
    • Newman DJ, Cragg GM (2004) Marine natural products and related compounds in clinical and advanced preclinical trials. J Nat Prod 67:1216–1238
    • (2004) J Nat Prod , vol.67 , pp. 1216-1238
    • Newman, D.J.1    Cragg, G.M.2
  • 19
    • 0035356381 scopus 로고    scopus 로고
    • Syntheses and transformations of α-azido ketones and related derivatives
    • PID: 11375029
    • Pàmies O, Bäckvall J-E (2001) Syntheses and transformations of α-azido ketones and related derivatives. J Org Chem 66:4022–4025
    • (2001) J Org Chem , vol.66 , pp. 4022-4025
    • Pàmies, O.1    Bäckvall, J.-E.2
  • 20
    • 0000119993 scopus 로고
    • A general and efficient synthesis of α-azido ketones
    • COI: 1:CAS:528:DyaK2cXjt1ahu7g%3D
    • Patonay T, Hoffman RV (1994) A general and efficient synthesis of α-azido ketones. J Org Chem 59:2902–2905
    • (1994) J Org Chem , vol.59 , pp. 2902-2905
    • Patonay, T.1    Hoffman, R.V.2
  • 21
    • 0036154219 scopus 로고    scopus 로고
    • Base-induced coupling of α-azido ketones with aldehydes - an easy and efficient route to trifunctionalized synthons 2-azido-3-hydroxy ketones
    • Patonay T, Juhász-Tóth E, Bényei A (2002) Base-induced coupling of α-azido ketones with aldehydes - an easy and efficient route to trifunctionalized synthons 2-azido-3-hydroxy ketones. Eur J Org Chem 2002:285–295
    • (2002) Eur J Org Chem , vol.2002 , pp. 285-295
    • Patonay, T.1    Juhász-Tóth, E.2    Bényei, A.3
  • 25
    • 20444377115 scopus 로고    scopus 로고
    • An asymmetric dihydroxylation route to (R)-(−)-octopamine, (R)-(−)-tembamide and (R)-(−)-aegeline
    • Sadyandy R, Fernandes RA, Kumar P (2005) An asymmetric dihydroxylation route to (R)-(−)-octopamine, (R)-(−)-tembamide and (R)-(−)-aegeline. ARKIVOC iii:36–43
    • (2005) ARKIVOC , vol.iii , pp. 36-43
    • Sadyandy, R.1    Fernandes, R.A.2    Kumar, P.3
  • 27
    • 70350131305 scopus 로고    scopus 로고
    • Production of laccase, manganese peroxidase and lignin peroxidase by Brazilian marine-derived fungi
    • Santos RCB, Durrant LR, Silva M, Sette LD (2010) Production of laccase, manganese peroxidase and lignin peroxidase by Brazilian marine-derived fungi. Enzym Microb Technol 46:32–37
    • (2010) Enzym Microb Technol , vol.46 , pp. 32-37
    • Santos, R.C.B.1    Durrant, L.R.2    Silva, M.3    Sette, L.D.4
  • 28
    • 77955981200 scopus 로고    scopus 로고
    • Potential biocatalysts originating from sea environments
    • COI: 1:CAS:528:DC%2BC3cXpvVyrtrs%3D
    • Trincone A (2010) Potential biocatalysts originating from sea environments. J Mol Catal B Enzym 66:241–256
    • (2010) J Mol Catal B Enzym , vol.66 , pp. 241-256
    • Trincone, A.1
  • 30
    • 72049105563 scopus 로고    scopus 로고
    • Asymmetric hydrogenation of simple ketones with planar chiral ruthenocenyl phosphinooxazoline ligands
    • COI: 1:CAS:528:DC%2BD1MXhsFaku73F
    • Wang Y, Liu D, Meng Q, Zhang W (2009) Asymmetric hydrogenation of simple ketones with planar chiral ruthenocenyl phosphinooxazoline ligands. Tetrahedron-Asymmetry 20:2510–2512
    • (2009) Tetrahedron-Asymmetry , vol.20 , pp. 2510-2512
    • Wang, Y.1    Liu, D.2    Meng, Q.3    Zhang, W.4
  • 31
    • 0035808832 scopus 로고    scopus 로고
    • A facile synthesis of (R)-(−)-2-azido1-aryethanols from 2-azido-1-arylketones using baker’s yeast
    • COI: 1:CAS:528:DC%2BD3MXhs1Ogtrg%3D
    • Yadav JS, Reddy BVS, Nanda S, Rao AB (2001) A facile synthesis of (R)-(−)-2-azido1-aryethanols from 2-azido-1-arylketones using baker’s yeast. Tetrahedron-Asymmetry 12:63–67
    • (2001) Tetrahedron-Asymmetry , vol.12 , pp. 63-67
    • Yadav, J.S.1    Reddy, B.V.S.2    Nanda, S.3    Rao, A.B.4
  • 32
    • 0037204732 scopus 로고    scopus 로고
    • Efficient enantioselective reduction ketones with Daucus carota root
    • COI: 1:CAS:528:DC%2BD38Xjt1Kku7w%3D, PID: 12027710
    • Yadav JS, Nanda S, Reddy BVS, Rao AB (2002) Efficient enantioselective reduction ketones with Daucus carota root. J Org Chem 67:3900–3903
    • (2002) J Org Chem , vol.67 , pp. 3900-3903
    • Yadav, J.S.1    Nanda, S.2    Reddy, B.V.S.3    Rao, A.B.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.