Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Clarence Wybon"'
Autor:
Karlijn Hollanders, Clarence Wybon, Charlène Gadais, Evelien Renders, Steven Ballet, Dario Masullo, Wouter A. Herrebout, Charlotte Martin, Laurent Van Raemdonck, Bert U. W. Maes
Publikováno v:
ACS catalysis
A chemoselective and catalytic transamidation for peptide synthesis is described. Transamidation under Zn catalysis is chemoselectively achieved by amino acid amide/peptidic amide derivatization with a tert-butyl nicotinate (tBu-nic) directing group.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ee88d807d481d220c3bedb894615ab4
https://biblio.vub.ac.be/vubir/zncatalyzed-nicotinatedirected-transamidations-in-peptide-synthesis(36ea1b70-c248-486b-bc88-0ad0d7233969).html
https://biblio.vub.ac.be/vubir/zncatalyzed-nicotinatedirected-transamidations-in-peptide-synthesis(36ea1b70-c248-486b-bc88-0ad0d7233969).html
Autor:
Evelien Renders, Thomas O. Ronson, Lieven Meerpoel, Xubin Wang, Clarence Wybon, Ben F. Van Steijvoort, Bert U. W. Maes, Hana Prokopcová
Publikováno v:
Angewandte Chemie: international edition in English
A new three‐component reductive arylation of amides with stable reactants (iPrOH and arylboronate esters), making use of a 2‐pyridinyl (Py) directing group, is described. The N‐Py‐amide substrates are readily prepared from carboxylic acids an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7003f9d4da040e75b759a7887bc7c9f
https://repository.uantwerpen.be/docman/irua/d3246b/154599_2019_11_01.pdf
https://repository.uantwerpen.be/docman/irua/d3246b/154599_2019_11_01.pdf
Autor:
Clarence Wybon, Charlène Gadais, Steven Ballet, Carl Mensch, Wouter A. Herrebout, Karlijn Hollanders, Bert U. W. Maes
Publikováno v:
ACS catalysis
A two-step catalytic amide-to-ester transformation of primary amides under mild reaction conditions has been developed. A tert-butyl nicotinate ( tBu nic) directing group is easily introduced onto primary amides via Pd-catalyzed amidation with tert-b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc070a486af7d78d51bf6be691d8db05
https://hdl.handle.net/10067/1471830151162165141
https://hdl.handle.net/10067/1471830151162165141
Autor:
Clarence Wybon, Charlène Gadais, Steven Ballet, Bert U. W. Maes, Laurent Van Raemdonck, Karlijn Hollanders, Evelien Renders
Publikováno v:
Proceedings of the 35th European Peptide Symposium.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5505bbc699250a4c8fa880d6fafb087f
https://doi.org/10.17952/35eps.2018.072
https://doi.org/10.17952/35eps.2018.072
Autor:
Norbert De Kimpe, Clarence Wybon, Gert Callebaut, Asta Žukauskaitė, Sven Mangelinckx, Algirdas Šačkus
Publikováno v:
Tetrahedron. 69:3437-3443
The convenient synthesis of 1,5-diazaspiro[2.3]hexanes, as new structurally challenging strained diazaspirocyclic compounds, was developed starting from easily accessible ethyl 2-(bromomethyl)-1-tosylaziridine-2-carboxylate. The key transformations i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa591a3f704d0d26f447efedbc3abbc7
https://doi.org/10.1016/j.tet.2013.02.065
https://doi.org/10.1016/j.tet.2013.02.065
Autor:
Clarence Wybon, Norbert De Kimpe, Gert Callebaut, Algirdas Šačkus, Asta Zukauskaite, Sven Mangelinckx
Publikováno v:
ChemInform. 44
The structurally new title compounds (VII) are synthesized from the easily accessible starting material (I) in eight steps.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3293323d5abfb77ac336209f4979b1dd
https://doi.org/10.1002/chin.201334091
https://doi.org/10.1002/chin.201334091