Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Philippe M. C. Roth"'
Publikováno v:
Frontiers in Chemical Engineering, Vol 3 (2021)
Despite their widespread use in the chemical industries, hydrogenation reactions remain challenging. Indeed, the nature of reagents and catalysts induce intrinsic safety challenges, in addition to demanding process development involving a 3-phase sys
Externí odkaz:
https://doaj.org/article/f93680483e2547008b4154eb95a83510
Publikováno v:
Organic Process Research & Development. 25:1589-1597
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98d3387bd133160768aeb1498f2ad519
https://doi.org/10.1021/acs.oprd.1c00008
https://doi.org/10.1021/acs.oprd.1c00008
Autor:
Oliver Reiser, Robert Eckl, Viktor Klöpfer, Joshua P. Barham, Philippe M. C. Roth, Johannes Floß
Publikováno v:
Green Chemistry. 23:6366-6372
Industrial process development is driven by several factors, including safety, cost, robustness and environmental aspects. However, attempts to establish aryl diazo esters – which are highly valued in academic research for their reactivity as carbe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab6cc59a3a73a58f478690b599c367bd
https://doi.org/10.1039/d1gc01624e
https://doi.org/10.1039/d1gc01624e
Autor:
Jason D. Williams, Günter Tekautz, Philippe M. C. Roth, C. Oliver Kappe, Marc Winter, Alexander Steiner, Franz J. Strauss, Guillaume Gauron
Publikováno v:
Organic Process Research & Development. 24:2208-2216
Although continuous flow technology can facilitate the scale-up of photochemical processes it is not yet routinely implemented on production scale in the fine chemical industries. This can be attri...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4522105fa7fc46b2cc830ea494a7e8ba
https://doi.org/10.1021/acs.oprd.0c00239
https://doi.org/10.1021/acs.oprd.0c00239
Autor:
Mélanie Roseau, Laëtitia Chausset-Boissarie, Sylvain Gremetz, Philippe M. C. Roth, Maël Penhoat
Publikováno v:
Photochemical & Photobiological Sciences
Photochemical & Photobiological Sciences, 2022, 21 (3), pp.421-432. ⟨10.1007/s43630-022-00171-w⟩
Photochemical & Photobiological Sciences, 2022, 21 (3), pp.421-432. ⟨10.1007/s43630-022-00171-w⟩
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24ed9cb04a8bea439e72a85bb3d2d63d
https://hal.science/hal-03861787
https://hal.science/hal-03861787
Autor:
Mélanie, Roseau, Laëtitia, Chausset-Boissarie, Sylvain, Gremetz, Philippe M C, Roth, Maël, Penhoat
Publikováno v:
Photochemicalphotobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology. 21(3)
The characterization of commercially available Corning
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1c092e7b036c940961959cf225112d22
https://pubmed.ncbi.nlm.nih.gov/35147919
https://pubmed.ncbi.nlm.nih.gov/35147919
Autor:
Philippe M. C. Roth, Sara Mattiello, Francesca Pallini, Luca Beverina, Mauro Sassi, Elena Sangalli
Carrying out photoredox direct arylation couplings between aryl halides and aryls in aqueous solutions of surfactants enables unprecedented selectivity with respect to the competing dehalogenation process, thanks to the partition coefficient of the s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b398d1acf5b39414a7c8c9da76a6e863
http://hdl.handle.net/10281/318800
http://hdl.handle.net/10281/318800
Publikováno v:
Nature Protocols. 9:104-111
This protocol describes the catalytic asymmetric formation of all-carbon quaternary centers--a distinctive feature of many natural products and pharmaceuticals--via conjugate addition of alkylzirconium reagents to a tertiary enone. This methodology u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dca919714e1b8fb7dda741fe7523d43b
https://doi.org/10.1038/nprot.2013.169
https://doi.org/10.1038/nprot.2013.169
Alkylzirconium reagents undergo highly enantioselective copper-catalysed 1,4-addition reaction to cyclic enones. These reactions use alkylmetal species generated in situ from alkenes and the Schwartz reagent, and do not require premade organometallic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7697768b1763eea1d092b2d53cf3d05
https://ora.ox.ac.uk/objects/uuid:fba47223-e388-4d32-8de1-233aceaf1e56
https://ora.ox.ac.uk/objects/uuid:fba47223-e388-4d32-8de1-233aceaf1e56
Catalytic asymmetric conjugate addition reactions with organometallic reagents are powerful reactions in synthetic chemistry. Procedures that use non-stabilized carbanions have been developed extensively, but these suffer from a number of limitations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76ab10ba6a77ac790b0ac21d02cb9169
https://doi.org/10.1038/nchem.1394
https://doi.org/10.1038/nchem.1394