Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Eva Baldaro"'
Autor:
Sara Cheroni, Luca Issi, Yves M. Galante, Eva Baldaro, Maurizio Gallucci, Cristina Formantici
Publikováno v:
Coloration Technology. 128:315-322
Guar galactomannan (referred to as guar gum) is a versatile polysaccharide, obtained from the seeds of the shrub Cyamopsis tetragonolobus, which finds several applications in either its native or chemically modified form. For textile printing, guar g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1af27cf5233661301e03604c53843615
https://doi.org/10.1111/j.1478-4408.2012.00382.x
https://doi.org/10.1111/j.1478-4408.2012.00382.x
Publikováno v:
Enzyme and Microbial Technology. 32:596-605
Two different catalases present in cell-free extracts of the yeast Trigonopsis variabilis have been separated by dye-binding chromatography. Both enzymes, named Tv C-I and Tv C-II, behave as members of the “typical catalases” family: they have a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c17bd9429cec3b13f232807922a95203
https://doi.org/10.1016/s0141-0229(03)00017-6
https://doi.org/10.1016/s0141-0229(03)00017-6
Publikováno v:
Biotechnology and Bioengineering. 70:239-244
A batch of the immobilized industrial biocatalyst glutaryl-7-ACA acylase (GA), one of the two enzymes involved in the biotransformation of cephalosporin C (CefC) into 7-aminocephalosporanic acid (7-ACA), was characterized. K(m) value for glutaryl-7-A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac8e277bac25df57cd25b77c52f1e018
https://doi.org/10.1002/1097-0290(20001020)70:2<239::aid-bit13>3.0.co
https://doi.org/10.1002/1097-0290(20001020)70:2<239::aid-bit13>3.0.co
Publikováno v:
Microbial Reagents in Organic Synthesis ISBN: 9789401050784
Non conventional applications of immobilized Penicillin G acylase with respect to its chemoselectivity and stereoselectivity are examined.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3aa7e5f3126973fd766910d469a5da4
https://doi.org/10.1007/978-94-011-2444-7_14
https://doi.org/10.1007/978-94-011-2444-7_14
Publikováno v:
Tetrahedron. 44:3685-3692
4-Vinyl-substituted oxamazins 15,16, and 3 have been prepared. Key steps of the synthesis are: the preparation of protected α-amino-β-hydroxyacid 6 through ester enolate condensation of ethyl glycinate STABASE adduct 8 with CH-protected propiolalde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4af1396b8a10c88ffeac7c9ec3ee64d3
https://doi.org/10.1016/s0040-4020(01)85998-6
https://doi.org/10.1016/s0040-4020(01)85998-6
Publikováno v:
ChemInform. 20
The phenylacetyloxymethylene group serves to protect the carboxyl group of benzylpenicillin sulphoxide (2a) during the transformation into 7-ADCA and 7β-amino-3-methoxyceph-3-em-4-carboxylic acid (9), being removed together with the 7-phenylacetyl s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30a5a34b8cc36cb452d4b5525ec43705
https://doi.org/10.1002/chin.198910349
https://doi.org/10.1002/chin.198910349
Publikováno v:
ChemInform. 19
4-Vinyl-substituted oxamazins 15,16, and 3 have been prepared. Key steps of the synthesis are: the preparation of protected α-amino-β-hydroxyacid 6 through ester enolate condensation of ethyl glycinate STABASE adduct 8 with CH-protected propiolalde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb10868bf942965c1643ee86db838056
https://doi.org/10.1002/chin.198844351
https://doi.org/10.1002/chin.198844351
Publikováno v:
Tetrahedron Letters. 29:4623-4624
The phenylacetyloxymethylene group serves to protect the carboxyl group of benzylpenicillin sulphoxide (2a) during the transformation into 7-ADCA and 7β-amino-3-methoxyceph-3-em-4-carboxylic acid (9), being removed together with the 7-phenylacetyl s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9219f75bec56d26d7ea546e7bda644ed
https://doi.org/10.1016/s0040-4039(00)80564-x
https://doi.org/10.1016/s0040-4039(00)80564-x