Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Francesco G. Mutti"'
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-11 (2019)
Amine dehydrogenases (AmDHs) catalyse the conversion of ketones into amines. Here, the authors created AmDH variants, the best of which showing a substrate-dependent stereo-switchable selectivity, affording either S- or R-configured amine products wi
Externí odkaz:
https://doaj.org/article/25ed70914fb742879be1c98e1f6f963c
Publikováno v:
Molecules, Vol 25, Iss 9, p 2140 (2020)
Comprising approximately 40% of the commercially available optically active drugs, α-chiral amines are pivotal for pharmaceutical manufacture. In this context, the enzymatic asymmetric amination of ketones represents a more sustainable alternative t
Externí odkaz:
https://doaj.org/article/effb1617463f47b4b2230c074264916f
Autor:
Jenő Gacs, Wuyuan Zhang, Tanja Knaus, Francesco G. Mutti, Isabel W.C.E. Arends, Frank Hollmann
Publikováno v:
Catalysts, Vol 9, Iss 4, p 305 (2019)
The consecutive photooxidation and reductive amination of various alcohols in a cascade reaction were realized by the combination of a photocatalyst and several enzymes. Whereas the photocatalyst (sodium anthraquinone-2-sulfonate) mediated the light-
Externí odkaz:
https://doaj.org/article/3e8671722e9b462daeb352f5a13d6d4d
Autor:
Francesco G. Mutti
Publikováno v:
Bioinorganic Chemistry and Applications, Vol 2012 (2012)
The oxidative cleavage of alkenes is classically performed by chemical methods, although they display several drawbacks. Ozonolysis requires harsh conditions (−78°C, for a safe process) and reducing reagents in a molar amount, whereas the use of p
Externí odkaz:
https://doaj.org/article/10b4838e0a1245b590d853535e77e2bf
Publikováno v:
Bioinorganic Chemistry and Applications, Vol 2008 (2008)
The biomimetic catalytic oxidations of the dinuclear and trinuclear copper(II) complexes versus two catechols, namely, D-(+)-catechin and L-(−)-epicatechin to give the corresponding quinones are reported. The unstable quinones were trapped by the n
Externí odkaz:
https://doaj.org/article/00787ebd63db4498b301b17fe203e4bc
Publikováno v:
ACS Catalysis, 12(23), 14459-14475. American Chemical Society
The efficient asymmetric catalytic synthesis of amines containing more than one stereogenic center is a current challenge. Here, we present a biocatalytic cascade that combines ene-reductases (EReds) with imine reductases/reductive aminases (IReds/Re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::761d3ce5e142370f75f4e13dc8344d0f
https://doi.org/10.1021/acscatal.2c03052
https://doi.org/10.1021/acscatal.2c03052
Publikováno v:
Organic Process Research and Development. 26(7):2085-2095
Enantiomerically pure 1,2-amino alcohols are important compounds due to their biological activities and wide applications in chemical synthesis. In this work, we present two multienzyme pathways for the conversion of l-phenylalanine into either 2-phe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::251c66406445ee453700d5e3b4ba1d53
https://hdl.handle.net/11245.1/4f6856a3-cda4-4f57-b63d-ded1bb12acf9
https://hdl.handle.net/11245.1/4f6856a3-cda4-4f57-b63d-ded1bb12acf9
Autor:
Yuxin Liu, Xingjun Zhu, Zheng Wei, Kefan Wu, Junfang Zhang, Francesco G. Mutti, Hong Zhang, Felix F. Loeffler, Jing Zhou
Publikováno v:
Angewandte Chemie.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0592b2d856ec5f8f8638925dbe69fae8
https://doi.org/10.1002/ange.202303570
https://doi.org/10.1002/ange.202303570
Autor:
Federico Croci, Jan Vilím, Theodora Adamopoulou, Vasilis Tseliou, Peter J. Schoenmakers, Tanja Knaus, Francesco G. Mutti
Publikováno v:
ChemBioChem, 23(22):e202200549. Wiley-VCH Verlag
Herein, we show how the merge of biocatalysis with flow chemistry aided by 3D-printing technologies can facilitate organic synthesis. This concept was exemplified for the reductive amination of benzaldehyde catalysed by co-immobilised amine dehydroge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f6b56c39e54782e4ca197a3cc4c5812
https://doi.org/10.1002/cbic.202200549
https://doi.org/10.1002/cbic.202200549
Publikováno v:
Chembiochem : a European journal of chemical biology. 23(17)
Peroxidase enzymes enable the construction of electrochemical sensors for highly sensitive and selective quantitative detection of various molecules, pathogens and diseases. Herein, we describe the immobilization of a peroxidase from Bacillus s. (BsD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d5b59d6b1a3e1ec855a5970f5d3b02d1
https://pubmed.ncbi.nlm.nih.gov/35723909
https://pubmed.ncbi.nlm.nih.gov/35723909