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pro vyhledávání: '"Viviána Nagy"'
Autor:
Mariann Szigeti, Enikő R. Tőke, Maria C. Turóczi, Viviána Nagy, György Szakács, and László Poppe
Publikováno v:
ARKIVOC, Vol 2008, Iss 3, Pp 54-65 (2007)
Externí odkaz:
https://doaj.org/article/71452bced9fd4f629b946360d68e23ed
Publikováno v:
Process Biochemistry. 45:1245-1250
Mixtures of specific structured lipids and phytosterol esters, valuable food components, were synthesized by an enzymatic one-pot process in organic-solvent-free medium starting from a mixture of phytosterol, caprylic acid and sunflower oil. Nine bio
Publikováno v:
Journal of the American Oil Chemists' Society. 84:907-915
Among numerous mesophilic fungi screened for sterol esterase activity followed by the esterification reaction between plant β-sitosterol and lauric acid in organic solvent, six Aspergillus strains were selected as the most active producers. These fu
Autor:
Viviána Nagy, Enikő R. Tőke, Ibrahim Che Omar, György Szakács, László Poppe, Darah Ibrahim, Gábor Szatzker, Lee Chee Keong
Publikováno v:
Journal of Molecular Catalysis B: Enzymatic. 39:141-148
Thirty-eight filamentous fungi cultivated under solid state fermentation (SSF) conditions were screened for lipase activity and enantioselectivity in kinetic resolutions of racemic secondary alcohols ( rac - 1a – c ) by acetylation with vinyl aceta
Autor:
György Szakács, and László Poppe, Maria Cristina Turoczi, Viviána Nagy, Enikő R. Tőke, Mariann Szigeti
Publikováno v:
Scopus-Elsevier
ARKIVOC, Vol 2008, Iss 3, Pp 54-65 (2007)
ARKIVOC, Vol 2008, Iss 3, Pp 54-65 (2007)
Several 4-aryl- and 4-heteroarylbut-3-en-2-ones (2a-c, bearing 4-phenyl-, 4-(furan-2-yl)- and 4-(1-benzyl-1H-indol-3yl)-substituents, respectively) were prepared by condensation reaction of acetone with the corresponding aldehydes (1a-c). Reduction o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d842ec436dde6b65a550f7a8b0f0d499
http://www.scopus.com/inward/record.url?eid=2-s2.0-39049172087&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-39049172087&partnerID=MN8TOARS