Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Florian Gérald Perrin"'
Autor:
Florian Gérald Perrin, Nicolai Cramer, Carl Thomas Bormann, Jin-Fay Tan, F. Mark Chadwick, Kay Severin
Publikováno v:
Journal of the American Chemical Society. 141:10372-10383
Densely substituted fused aromatic triazenes can be prepared by [2 + 2 + 2] cyclotrimerization reactions of 1-alkynyl triazenes. The Cp*Ru-catalyzed cyclization proceeds well with both simple alkynyl triazenes and tethered 1-diynyl triazenes. Attract
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d571d454a87545366ddd324993ca1e0
https://doi.org/10.1021/jacs.9b04111
https://doi.org/10.1021/jacs.9b04111
Autor:
Rosario Scopelliti, Florian Gérald Perrin, Nicolai Cramer, Kay Severin, Abdusalom A. Suleymanov, Gregor Kiefer, David Kossler
Publikováno v:
Angewandte Chemie. 129:11648-11651
Vinyl triazenes were obtained by enantioselective [2+2] cycloaddition reactions of bicyclic alkenes with 1-alkynyl triazenes in the presence of a RuII catalyst with a chiral cyclopentadienyl ligand. These triazenes serve as unique vinyl cation surrog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13c3b22f37f587bfa4d93edc3fd30af7
https://doi.org/10.1002/ange.201706013
https://doi.org/10.1002/ange.201706013
Autor:
Rosario Scopelliti, Gregor Kiefer, Sophie Racine, Loïc Jeanbourquin, Daniele Perrotta, Florian Gérald Perrin, Kay Severin, Jerome Waser
Publikováno v:
ChemInform. 47
The versatile reactivity of 1-alkynyltriazenes is demonstrated by reactions with acids, acyl chlorides, tetracyanoethylene, and cyclopropanes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d21162c5471c23368337c5064299b68
https://doi.org/10.1002/chin.201611074
https://doi.org/10.1002/chin.201611074
Autor:
Daniele Perrotta, Loïc Jeanbourquin, Sophie Racine, Florian Gérald Perrin, Rosario Scopelliti, Kay Severin, Gregor Kiefer, Jerome Waser
Publikováno v:
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
The chemical reactivity of 1-alkynyltriazenes has been investigated and is found to parallel the reactivity of ynamides. The similarity in reactivity of these two classes of compounds is demonstrated by addition reactions with acids, by cycloaddition
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a568bb4f51a403a17802073fa8adcb79
https://infoscience.epfl.ch/record/211258
https://infoscience.epfl.ch/record/211258
Autor:
Gábor Laurenczy, Sergey A. Katsyuba, Zhaofu Fei, Rosario Scopelliti, Florian Gérald Perrin, Paul J. Dyson, Felix D. Bobbink, Emilia Păunescu
An ionic liquid encompassing a bulky tertiary amine was synthesized and used as a dual solvent-reactant for the formation of a frustrated Lewis pair with tris(pentafluorophenyl) borane, forming a pseudo-frustrated Lewis pair-ionic liquid system. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9944a00070d23a4c038c74c7e74df1a5
https://infoscience.epfl.ch/record/234016
https://infoscience.epfl.ch/record/234016