Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ádám Gyömöre"'
Publikováno v:
ACS Sustainable Chemistry & Engineering. 6:10869-10875
An exo-selective catalytic Diels–Alder reaction was developed using a Lewis acid catalyst with size-exclusion structural design. Exploiting the steric effect, especially the steric attraction, the Lewis acid catalyst was able to reroute the reactio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2eaa1897feeeb84a7335cc0661475062
https://doi.org/10.1021/acssuschemeng.8b02099
https://doi.org/10.1021/acssuschemeng.8b02099
Publikováno v:
Journal of Organometallic Chemistry. 847:258-262
• Combined computational and experimental work to probe Lewis acidity of some boranes to be used in FLP hydrogenation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a8f0113e5eda95ed525838aa2d4785ce
https://doi.org/10.1016/j.jorganchem.2017.04.031
https://doi.org/10.1016/j.jorganchem.2017.04.031
Publikováno v:
ACS Catalysis. 5:5366-5372
In this paper, we report on the development of a bench-stable borane for frustrated Lewis pair catalyzed reduction of aldehydes, ketones, and enones. The deliberate fine-tuning of structural and electronic parameters of Lewis acid component and the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ba76275d25c8a704ce0d53de0d3caf3
https://doi.org/10.1021/acscatal.5b01299
https://doi.org/10.1021/acscatal.5b01299
Publikováno v:
Angewandte Chemie (International ed. in English). 56(19)
Herein we report that a single frustrated Lewis pair (FLP) catalyst can promote the reductive etherification of aldehydes and ketones. The reaction does not require an exogenous acid catalyst, but the combined action of FLP on H2, R-OH or H2O generat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::102c874b00f5a3882ef69b3a07d052bd
https://pubmed.ncbi.nlm.nih.gov/28378401
https://pubmed.ncbi.nlm.nih.gov/28378401
Autor:
Ádám Gyömöre, Antal Csámpai
Publikováno v:
Journal of Organometallic Chemistry. 696:1626-1631
A series of planar chiral ferroceno[d]pyridazinones was prepared by hydrazine-mediated cyclisations of (Sp)-2-formylferrocenoyl fluoride obtained in two steps from (2S,4S)-4-(methoxymethyl)-2-ferrocenyl-1,3-dioxane. Further derivatives based on the n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ddecda7b6b115e46e436041967722748
https://doi.org/10.1016/j.jorganchem.2011.01.032
https://doi.org/10.1016/j.jorganchem.2011.01.032
Publikováno v:
Tetrahedron. 64:10837-10848
By means of base-catalyzed ring enlargement of triazaindenoindenes and pentalenoindenes obtained from anhydride-induced ring transformation of 3,4-dihydro-2H-pyrimido- and 2,3-dihydroimidazo[2,1-a]phthalazinium-olates, respectively, a series of pyraz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1462deb735331a4f433a07d5302e7e28
https://doi.org/10.1016/j.tet.2008.09.020
https://doi.org/10.1016/j.tet.2008.09.020