Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Mohamed, Amedjkouh"'
Publikováno v:
Chirality. 32:1143-1151
Experimental and kinetic analysis of a chemical system combines autocatalytic amplification of 2-alkynyl-5-pyrimidyl alkanol 2 and 6-alkynyl-3-pyridyl akanol 4 in which 2 acts as a chiral trigger and 4 being the subsequent autocatalyst. Starting from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::404a0d98e4d63e9d12f45d0e3cc4d12a
https://doi.org/10.1002/chir.23256
https://doi.org/10.1002/chir.23256
Autor:
Mohamed Amedjkouh, Giuseppe Rotunno
Publikováno v:
Asymmetric Autocatalysis ISBN: 9781839162619
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::162d1e82ea0ee608ad727d5275fae376
https://doi.org/10.1039/9781839166273-00289
https://doi.org/10.1039/9781839166273-00289
Autor:
Isabelle, Gerz, Sergio Augusto Venturinelli, Jannuzzi, Knut T, Hylland, Chiara, Negri, David S, Wragg, Sigurd, Øien-Ødegaard, Mats, Tilset, Unni, Olsbye, Serena, DeBeer, Mohamed, Amedjkouh
Publikováno v:
European journal of inorganic chemistry. 2021(46)
A series of Cu(I) complexes of bidentate or tetradentate Schiff base ligands bearing either 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::17cae16d38b764247ef8f04aaf80d1a2
https://pubmed.ncbi.nlm.nih.gov/35874966
https://pubmed.ncbi.nlm.nih.gov/35874966
Autor:
Mohamed Amedjkouh, Giuseppe Rotunno
Absolute asymmetric synthesis produces chiral molecules without any chiral polarization and is an interesting rational for the origin of homochirality. Remarkably, in the Soai reaction absolute asymmetric amplification of alkanol product is observed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f21f57af25a44ea0cb135114217191e
https://doi.org/10.33774/chemrxiv-2021-ls95s
https://doi.org/10.33774/chemrxiv-2021-ls95s
Autor:
Sigurd Øien-Ødegaard, Mohamed Amedjkouh, David S. Wragg, Unni Olsbye, Chiara Negri, Mats Tilset, Isabelle Gerz
A modular one-pot synthesis yielding tetracoordinated-N,N,N,N-copper(I) complexes bearing imine and diimine ligands was developed. Copper aids the condensation of a pyridine or imidazole carbaldehyde with a biphenyl amine and even stabilizes labile l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ae38973b7f75133c63d28a1b2057a50
https://doi.org/10.26434/chemrxiv.13727857
https://doi.org/10.26434/chemrxiv.13727857
Publikováno v:
Chemistry, an Asian Journal
Symmetry breaking is observed in the Soai reaction in a confinement environment provided by zirconium‐based UiO‐MOFs used as crystalline sponges. Subsequent reaction of encapsulated Soai aldehyde with Zn(i‐Pr)2 vapour promoted absolute asymmetr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::291692a7c3bb17bd9e865264f8bea981
http://hdl.handle.net/10852/92750
http://hdl.handle.net/10852/92750
We report a novel vapour phase procedure to perform the Soai reaction in an absolute asymmetric synthesis fashion: the substrate is confined in the pores of the UiO-type MOFs, and vapour phase reactions with Zn(i-Pr)2 are performed in a sealed enviro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d32d655c216a10d628abca9e0fdf330
https://doi.org/10.26434/chemrxiv.13503369
https://doi.org/10.26434/chemrxiv.13503369
Publikováno v:
ChemSystemsChem. 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91f99bf072b5fac9331cdd004dbf2665
https://doi.org/10.1002/syst.201900060
https://doi.org/10.1002/syst.201900060
Autor:
Gurpreet Kaur, Eirik Mydske Thoresen, Mohamed Amedjkouh, Karl Petter Lillerud, Sigurd Øien-Ødegaard, Mats Tilset
Four different ruthenium(II) complexes were incorporated into the metal–organic framework (MOF) UiO-67 using three different synthetic strategies: premade linker synthesis, postsynthetic functionalization, and postsynthetic linker exchange. One of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fb46935771b1f2137b78cbd7c16d2e7
http://hdl.handle.net/10852/84176
http://hdl.handle.net/10852/84176
Publikováno v:
Monatshefte für Chemie - Chemical Monthly. 150:49-58
A potential intermediate in the synthesis of several trans-clerodane natural products has been constructed employing a Diels–Alder reaction as a key-step. Two epimeric exo-adducts were formed in a 4:3 ratio in an EtAlCl2-mediated cycloaddition of O
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e05f3df900f7f084b84de517f3f0c2b9
https://doi.org/10.1007/s00706-018-2277-9
https://doi.org/10.1007/s00706-018-2277-9