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pro vyhledávání: '"Tommaso Quinto"'
Nicotinamide adenine dinucleotide (NADH) and nicotinamide adenine dinucleotide phosphate constitute a major cost factor in preparative biotransformations. The development of efficient methods for their regeneration with cheap reducing equivalents has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da24cc9dd3738b0cbcae9460c39f5a65
http://doc.rero.ch/record/324736/files/11244_2013_Article_187.pdf
http://doc.rero.ch/record/324736/files/11244_2013_Article_187.pdf
Autor:
Thomas R. Ward, Valentin Köhler, Tommaso Quinto, Albert Morina, Jeremy M. Zimbron, Fabian Schwizer
Publikováno v:
ChemCatChem. 6:1010-1014
We report on the optimization of an artificial imine reductase based on the biotin-streptavidin technology. With the aim of rapidly generating chemical diversity, a novel strategy for the formation and evaluation of biotinylated complexes is disclose
Autor:
Diego Ghislieri, Thomas R. Ward, Nicholas J. Turner, Ekaterina Churakova, Yvonne M. Wilson, Livia Knörr, Daniel Häussinger, Tommaso Quinto, Marc Dürrenberger, Valentin Köhler, Frank Hollmann
Publikováno v:
Nature Chemistry. 5:93-99
Enzymatic catalysis and homogeneous catalysis offer complementary means to address synthetic challenges, both in chemistry and in biology. Despite its attractiveness, the implementation of concurrent cascade reactions that combine an organometallic c
Publikováno v:
ChemCatChem. 2:661-665
Sequential dual-metal catalyzed reactions are successfully applied to create chemical diversity in indole polycyclic alkaloids. Gold-catalyzed intramolecular allylic alkylation of indoles with alcohols, followed by Ru-assisted ring-closing metathesis
Publikováno v:
Organicbiomolecular chemistry. 13(2)
Stereoselectively labelled isotopomers of NAD(P)H are highly relevant for mechanistic studies of enzymes which utilize them as redox equivalents. Whereas several methods are firmly established for their generation in high diastereomeric purity by enz
Publikováno v:
ChemInform. 37
A new class of chiral C 1 -symmetrical di-amino-oligothiophene ligands easy-grafted on a soluble polymeric support (MeOPEG 5000 ) is described. The diamines were found to be effective promoting agents for the [Pd(0)]-catalysed asymmetric allylic alky
Autor:
Valentin Köhler, Jeremy M. Zimbron, Fabian Schwizer, Thomas R. Ward, Albert Morina, Tommaso Quinto
Publikováno v:
ChemCatChem. 6:1120-1120
Publikováno v:
Advanced Synthesis & Catalysis; Aug2006, Vol. 348 Issue 12/13, p1521-1527, 7p