| dc.date | 2015 | |
| dc.date | 2016-06-03T20:13:39Z | |
| dc.date | 2016-06-03T20:13:39Z | |
| dc.date.accessioned | 2018-03-29T01:32:46Z | |
| dc.date.available | 2018-03-29T01:32:46Z | |
| dc.identifier | | |
| dc.identifier | Marine Biotechnology. Springer New York Llc, v. 17, n. 6, p. 736 - 742, 2015. | |
| dc.identifier | 14362228 | |
| dc.identifier | 10.1007/s10126-015-9644-x | |
| dc.identifier | http://www.scopus.com/inward/record.url?eid=2-s2.0-84946498362&partnerID=40&md5=6b997d6e3aae59263c364521395bb195 | |
| dc.identifier | http://repositorio.unicamp.br/jspui/handle/REPOSIP/238097 | |
| dc.identifier | 2-s2.0-84946498362 | |
| dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/1304758 | |
| dc.description | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
| dc.description | Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) | |
| dc.description | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
| dc.description | Seven strains of marine-derived fungi (Aspergillus sclerotiorum CBMAI 849, Cladosporium cladosporioides CBMAI 857, Penicillium raistrickii CBMAI 931, Penicillium citrinum CBMA 1186, Mucor racemosus CBMAI 847, Beauveria felina CBMAI 738, and Penicillium oxalicum CBMAI 1185) and terrestrial fungus Penicillium chrysogenum CBMA1199 were screened as catalysts for the asymmetric reduction of α-keto azides 5–8 to their corresponding β-azidophenylethanols 9–12. The marine fungi showed Prelog and anti-Prelog selectivities to the reduction α-keto azides 5–8. The fungi A. sclerotiorum CBMAI 849, C. cladosporioides CBMAI 857, P. raistrickii CBMAI 931, and P. citrinum CBMA 1186 catalyzed the reduction of azido ketone 6 to the corresponding (R)-2-azido-1-(4-methoxyphenyl)ethanol (10) with good conversions (68–100 %) and excellent enantiomeric excesses (>99 % ee) according to Prelog rule. © 2015, Springer Science+Business Media New York. | |
| dc.description | 17 | |
| dc.description | 6 | |
| dc.description | 736 | |
| dc.description | 742 | |
| dc.description | CNPq, Fundação de Amparo à Pesquisa do Estado de São Paulo | |
| dc.description | FAPESP, Fundação de Amparo à Pesquisa do Estado de São Paulo | |
| dc.description | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
| dc.description | Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) | |
| dc.description | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
| dc.description | Ankati, H., Yang, Y., Zhu, D., Biehl, E.R., Hua, L., Synthesis of optically pure 2-azido-1-arylethanols with isolated enzymes and conversion to triazole-containing β-blocker analogues employing click chemistry (2008) J Org Chem, 73, pp. 6433-6436. , COI: 1:CAS:528:DC%2BD1cXosFKltrg%3D, PID: 18630881 | |
| dc.description | Antranikian, G., Vorgias, C.E., Bertoldo, C., Extreme environments as a resource for microorganisms and novel biocatalysts (2005) Adv Biochem Eng Biotech, 96, pp. 219-262. , COI: 1:CAS:528:DC%2BD2MXhtlamsr%2FN | |
| dc.description | Besse, P., Veschambre, H., Chênevert, R., Dickman, M., Chemoenzymatic synthesisof chiral β-azidoalcohols. Application to the preparation of chiral aziridines and aminoalcohols (1994) Tetrahedron-Asymmetry, 5, pp. 1727-1744 | |
| dc.description | Bisogno, F.R., Lavandera, I., Kroutil, W., Gotor, V., Tandem concurrent processes: one-pot single-catalyst biohydrogen transfer for the simultaneous preparation of enantiopure secondary alcohols (2009) J Org Chem, 74, pp. 1730-1732. , COI: 1:CAS:528:DC%2BD1MXksVylsA%3D%3D, PID: 19138072 | |
| dc.description | Brenelli, E.C.S., Fernandes, J.L.N., Stereoselective acylations of 1,2-azidoalcohols with vinyl acetate, catalyzed by lipase Amano OS (2003) Tetrahedron-Asymmetry, 14, pp. 1255-1259. , COI: 1:CAS:528:DC%2BD3sXksFGmsLk%3D | |
| dc.description | Bugni, T.S., Ireland, C.M., Marine-derived fungi: a chemically and biologically diverse group of microorganisms (2004) Nat Prod Rep, 21, pp. 143-163. , COI: 1:CAS:528:DC%2BD2cXisFWgtb8%3D, PID: 15039840 | |
| dc.description | Cheng, Z., Pan, J., Tang, W., Chen, Q., Lin, Y., Biodiversity and biotechnological potential of mangrove-associated fungi (2009) J For Res, 20, pp. 63-72. , COI: 1:CAS:528:DC%2BD1MXisFChs7c%3D | |
| dc.description | De Vita-Marques, A.M., Lira, S.P., Berlinck, R.G.S., Seleghim, M.H.R., Sponchiado, S.R.P., Tauk-Tornisielo, S.M., Barata, M., Sette, L.D., A multi-screening approach for marine-derived fungal metabolites and the isolation of cyclodepsipeptides from Beauveria felina (2008) Quim Nova, 31, pp. 1099-1103 | |
| dc.description | Fardelone, L.C., Rodrigues, J.A.R., Moran, P.J.S., Bioreduction of 2-azido-1-arylethanones mediated by Geotrichum candidum and Rhodotorula glutinis (2006) J Mol Catal B Enzym, 39, pp. 9-12. , COI: 1:CAS:528:DC%2BD28Xjs1Khtrw%3D | |
| dc.description | Gavrilescua, M., Chisti, Y., Biotechnology - a sustainable alternative for chemical industry (2005) Biotechnol Adv, 23, pp. 471-499 | |
| dc.description | Hans-Peter, M., Werbitzky, O., How green can the industry become with biotechnology (2011) Biocatalysis for green chemistry and chemical process development, , Junhua AT, Kazlauskas R, (eds), Wiley, Hoboken | |
| dc.description | Kamal, A., Shaik, A.A., Sandbhor, M., Malik, M.S., Synthesis of enantiopure β-azidoalcohols from their ketoazides by reduction with NaBH4 in the presence of alumina and in situ lipase resolution (2004) Tetrahedron-Asymmetry, 15, pp. 935-939. , COI: 1:CAS:528:DC%2BD2cXhvV2is7o%3D | |
| dc.description | Kamal, A., Shaik, A.A., Sandbhor, M., Malik, M.S., Chemoenzymatic synthesis of (R)- and (S)-tembamide, aegeline and denopamine by a one-pot lipase resolution protocol (2004) Tetrahedron-Asymmetry, 15, pp. 3939-3944. , COI: 1:CAS:528:DC%2BD2cXhtVKrsLzE | |
| dc.description | Liu, Z., Weis, R., Gliede, A., Enzymes from higher eukaryotes for industrial biocatalysis (2004) Food Technol Biotechnol, 42, pp. 237-249. , COI: 1:CAS:528:DC%2BD2MXhsV2hsLY%3D | |
| dc.description | Martins, M.P., Mouad, A.M., Boschini, L., Seleghim, M.H.R., Sette, L.D., Porto, A.L.M., Marine fungi Aspergillus sydowii and Trichoderma sp. catalyze the hydrolysis of benzyl glycidyl ether (2011) Mar Biotechnol, 13, pp. 14-20 | |
| dc.description | Matsuda, T., Yamanaka, R., Nakamura, K., Recent progress in biocatalysis for asymmetric oxidation and reduction (2009) Tetrahedron-Asymmetry, 20, pp. 513-557. , COI: 1:CAS:528:DC%2BD1MXltl2ksr4%3D | |
| dc.description | Mesas-Sánchez, L., Díaz-Álvarez, A.E., Dinér, P., Non-enzymatic kinetic resolution of 1,2-azidoalcohols using a planar-chiral DMAP derivative catalyst (2013) Tetrahedron, 69, pp. 753-757 | |
| dc.description | Newman, D.J., Cragg, G.M., Marine natural products and related compounds in clinical and advanced preclinical trials (2004) J Nat Prod, 67, pp. 1216-1238. , COI: 1:CAS:528:DC%2BD2cXkslWhtbo%3D, PID: 15332835 | |
| dc.description | Pàmies, O., Bäckvall, J.-E., Syntheses and transformations of α-azido ketones and related derivatives (2001) J Org Chem, 66, pp. 4022-4025. , PID: 11375029 | |
| dc.description | Patonay, T., Hoffman, R.V., A general and efficient synthesis of α-azido ketones (1994) J Org Chem, 59, pp. 2902-2905. , COI: 1:CAS:528:DyaK2cXjt1ahu7g%3D | |
| dc.description | Patonay, T., Juhász-Tóth, E., Bényei, A., Base-induced coupling of α-azido ketones with aldehydes - an easy and efficient route to trifunctionalized synthons 2-azido-3-hydroxy ketones (2002) Eur J Org Chem, 2002, pp. 285-295 | |
| dc.description | Pavia, D.L., Lampman, G.M., Kriz, G.S., Engel, R.G., (1999) Introduction to organic laboratory techniques, , Sunders College Publishing, Orlando | |
| dc.description | Rocha, L.C., Ferreira, H.V., Pimenta, E.F., Berlinck, R.G.S., Seleghim, M.H.R., Javaroti, D.C.D., Sette, L.D., Porto, A.L.M., Bioreduction of α-chloroacetophenone by whole cells of marine fungi (2009) Biotechnol Lett, 31, pp. 1559-1563. , COI: 1:CAS:528:DC%2BD1MXhtFensbfI, PID: 19495566 | |
| dc.description | Rocha, L.C., Ferreira, H.V., Pimenta, E.F., Berlinck, R.G.S., Rezende, M.O.O., Landgraf, M.D., Seleghim, M.H.R., Porto, A.L.M., Biotransformation of α-bromoacetophenones by the marine fungus Aspergillus sydowii (2010) Mar Biotechnol, 12, pp. 552-557. , COI: 1:CAS:528:DC%2BC3cXht1Cns7vJ, PID: 19941024 | |
| dc.description | Sadyandy, R., Fernandes, R.A., Kumar, P., An asymmetric dihydroxylation route to (R)-(−)-octopamine, (R)-(−)-tembamide and (R)-(−)-aegeline (2005) ARKIVOC, iii, pp. 36-43 | |
| dc.description | San-Martín, A., Rovirosa, J., Astudillo, L., Sepúlveda, B., Ruiz, D., San-Martín, C., Biotransformation of the marine sesquiterpene pacifenol by a facultative marine fungus (2008) Nat Prod Res, 22, pp. 1627-1632. , PID: 19085420 | |
| dc.description | Santos, R.C.B., Durrant, L.R., Silva, M., Sette, L.D., Production of laccase, manganese peroxidase and lignin peroxidase by Brazilian marine-derived fungi (2010) Enzym Microb Technol, 46, pp. 32-37 | |
| dc.description | Trincone, A., Potential biocatalysts originating from sea environments (2010) J Mol Catal B Enzym, 66, pp. 241-256. , COI: 1:CAS:528:DC%2BC3cXpvVyrtrs%3D | |
| dc.description | Veberlen, P.J., De Schutter, D.P., Delvaux, F., Verstrepen, K.J., Delvau, F.R., Immobilized yeast cell systems for continuous fermentation applications (2006) Biotechnol Lett, 28, pp. 1515-1525 | |
| dc.description | Wang, Y., Liu, D., Meng, Q., Zhang, W., Asymmetric hydrogenation of simple ketones with planar chiral ruthenocenyl phosphinooxazoline ligands (2009) Tetrahedron-Asymmetry, 20, pp. 2510-2512. , COI: 1:CAS:528:DC%2BD1MXhsFaku73F | |
| dc.description | Yadav, J.S., Reddy, B.V.S., Nanda, S., Rao, A.B., A facile synthesis of (R)-(−)-2-azido1-aryethanols from 2-azido-1-arylketones using baker’s yeast (2001) Tetrahedron-Asymmetry, 12, pp. 63-67. , COI: 1:CAS:528:DC%2BD3MXhs1Ogtrg%3D | |
| dc.description | Yadav, J.S., Nanda, S., Reddy, B.V.S., Rao, A.B., Efficient enantioselective reduction ketones with Daucus carota root (2002) J Org Chem, 67, pp. 3900-3903. , COI: 1:CAS:528:DC%2BD38Xjt1Kku7w%3D, PID: 12027710 | |
| dc.description | | |
| dc.description | | |
| dc.language | en | |
| dc.publisher | Springer New York LLC | |
| dc.relation | Marine Biotechnology | |
| dc.rights | fechado | |
| dc.source | Scopus | |
| dc.title | Stereoselective Bioreduction Of α-azido Ketones By Whole Cells Of Marine-derived Fungi | |
| dc.type | Artículos de revistas | |
