Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Huu Vinh Trinh"'
Autor:
Kosuke Tsuzuki, Michael Faundo, Huu Vinh Trinh, Thomas Louis-Goff, Arnold L. Rheingold, John M. Berestecky, Axel T. Lehrer, Jakub Hyvl
Publikováno v:
Results in Chemistry, Vol 5, Iss , Pp 100953- (2023)
Novel heteroleptic triarylbismuthane amides of Ar12Ar2Bi formula where Ar2 contains an amide functional group were tested for antimicrobial activity against various bacterial isolates: S. aureus, methicillin-resistant S. aureus (MRSA), S. pyogenes, E
Externí odkaz:
https://doaj.org/article/00cba392630b41179bdfe2a96096d6ac
Publikováno v:
Materials Research Express, Vol 10, Iss 3, p 035101 (2023)
Plastic pollution and energy consumption are two of the most significant problems facing modern society. While the non-degradability of plastic leaves negative impacts on Earth’s ecosystem, fossil fuel usage as an energy source greatly contributes
Externí odkaz:
https://doaj.org/article/986f5335cf4343869e91544edfb70f62
Autor:
Thomas Louis-Goff, Huu Vinh Trinh, Eileen Chen, Arnold L. Rheingold, Christian Ehm, Jakub Hyvl
Publikováno v:
ACS Catalysis. 12:3719-3730
An efficient, catalytic difluorocarbenation of olefins to give 1,1-difluorocyclopropanes is presented. The catalyst, an organobismuth complex, uses TMS-CF3 as a stoichiometric difluorocarbene source. We demonstrate both the viability and robustness o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85054cc2aab2355f329c506b4950ff6b
https://doi.org/10.1021/acscatal.1c05959
https://doi.org/10.1021/acscatal.1c05959
Publikováno v:
ChemPlusChem. 88
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2cbc959997c4bcfea4cd17ea68a8aace
https://doi.org/10.1002/cplu.202200450
https://doi.org/10.1002/cplu.202200450
Akademický článek
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Autor:
Thomas Louis-Goff, Huu Vinh Trinh, Eileen Chen, Arnold L. Rheingold, Christian Ehm, Jakub Hyvl
A new, efficient, catalytic difluorocarbenation of olefins to give 1,1-difluorocyclopropanes is presented. The catalyst, an organobismuth complex, uses TMSCF3 as a stoichiometric difluorocarbene source. We demonstrate both the viability and robustnes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8436d08cfd515d7446366534f2c1798a
https://doi.org/10.26434/chemrxiv.13424117.v1
https://doi.org/10.26434/chemrxiv.13424117.v1
Publikováno v:
European Journal of Organic Chemistry. 2016:2944-2953
We report the development of the intramolecular Julia olefination of imides. This original reaction produces N-fused bicyclic enamide compounds, which are interesting precursors in the synthesis of alkaloids. We show that this transformation enables
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30f558fec791afa60eba22016b4ec9f5
https://doi.org/10.1002/ejoc.201600349
https://doi.org/10.1002/ejoc.201600349
Publikováno v:
Organometallics
Organometallics, American Chemical Society, 2017, 36 (1), pp.129-135. ⟨10.1021/acs.organomet.6b00535⟩
Organometallics, American Chemical Society, 2017, 36 (1), pp.129-135. ⟨10.1021/acs.organomet.6b00535⟩
International audience; The substitution of biarylphosphine ligands was shown to have a marked impact on the α/β selectivity of the arylation of ester enolates. To get further insight into this effect, the solid-state structures of arylpalladium br
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d36d5c9835e3b74ffa5da313a721dbd2
https://edoc.unibas.ch/57660/
https://edoc.unibas.ch/57660/
Publikováno v:
ChemInform. 47
We report the development of the intramolecular Julia olefination of imides. This original reaction produces N-fused bicyclic enamide compounds, which are interesting precursors in the synthesis of alkaloids. We show that this transformation enables
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37a4b677e90f59cab2aa004874d11648
https://doi.org/10.1002/chin.201644053
https://doi.org/10.1002/chin.201644053
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2016, 18 (19), pp.4790-4793. ⟨10.1021/acs.orglett.6b02160⟩
Organic Letters, American Chemical Society, 2016, 18 (19), pp.4790-4793. ⟨10.1021/acs.orglett.6b02160⟩
International audience; The preparation of exo-enol esters from cyclic anhydrides is reported using a modified Julia olefination. The reaction is highly stereoselective. The Smiles rearrangement can be performed in a one-pot process, giving a straigh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::209fd9ab3d17d68b6b1d61adee1fa204
https://hal-udl.archives-ouvertes.fr/hal-02122513
https://hal-udl.archives-ouvertes.fr/hal-02122513