Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Vuk D. Vuković"'
Autor:
Andrei Golushko, Florent Noël, Shaofei Zhang, Marie Vayer, Nazanin Rezajooei, Christopher N. Rowley, Vuk D. Vuković, Joseph Moran, David Lebœuf
Publikováno v:
Chem
Chem, Cell Press, In press, ⟨10.1016/j.chempr.2021.10.023⟩
Chem, In press, ⟨10.1016/j.chempr.2021.10.023⟩
Chem, Cell Press, In press, ⟨10.1016/j.chempr.2021.10.023⟩
Chem, In press, ⟨10.1016/j.chempr.2021.10.023⟩
International audience; Alcohols and epoxides are arguably ideal electrophiles for the Friedel-Crafts alkylation, since they are widely available, require no pre-activation, and produce no stoichiometric waste beyond water. However, neither primary a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ebc8665e3f91485434ed0a4bf84dcf8
https://doi.org/10.1016/j.chempr.2021.10.023
https://doi.org/10.1016/j.chempr.2021.10.023
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, 2019, 84 (24), pp.15926-15947. ⟨10.1021/acs.joc.9b02398⟩
Journal of Organic Chemistry, American Chemical Society, 2019, 84 (24), pp.15926-15947. ⟨10.1021/acs.joc.9b02398⟩
The Journal of Organic Chemistry
Journal of Organic Chemistry, 2019, 84 (24), pp.15926-15947. ⟨10.1021/acs.joc.9b02398⟩
Journal of Organic Chemistry, American Chemical Society, 2019, 84 (24), pp.15926-15947. ⟨10.1021/acs.joc.9b02398⟩
The Journal of Organic Chemistry
A general method to access CF3-substituted allenes from propargylic alcohols under Lewis acid catalysis in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) as solvent is described. By tuning the reaction t...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::985ee51f69db09ca1f6b63f555812d4c
https://hal.science/hal-02516523
https://hal.science/hal-02516523
Publikováno v:
Chemical Science
Ring-opening hydroarylation of cyclopropanes is typically limited to substrates bearing a donor–acceptor motif. Here, the transformation is achieved for monosubstituted cyclopropanes by using catalytic Brønsted acid in hexafluoroisopropanol (HFIP)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::297a6f6703caca823976c0c3ffa2def8
https://doi.org/10.1039/c8sc02126k
https://doi.org/10.1039/c8sc02126k
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2018, 20 (3), pp.574-577. ⟨10.1021/acs.orglett.7b03688⟩
Organic Letters, 2018, 20 (3), pp.574-577. ⟨10.1021/acs.orglett.7b03688⟩
Organic Letters, American Chemical Society, 2018, 20 (3), pp.574-577. ⟨10.1021/acs.orglett.7b03688⟩
Organic Letters, 2018, 20 (3), pp.574-577. ⟨10.1021/acs.orglett.7b03688⟩
This project has received funding from the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation programme (grant agreement n° 639170) and by grants from LabEx “Chemistry of Complex Systems”. V.D.V. than
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19d353af676a63a13ece3e486bb8fcd9
Publikováno v:
Angewandte Chemie International Edition
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2017, 56 (11), pp.3085-3089. ⟨10.1002/anie.201612573⟩
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2017, 56 (11), pp.3085-3089. ⟨10.1002/anie.201612573⟩
International audience; Highly electronically deactivated benzylic alcohols, including those with a CF3 group adjacent to the OH-bearing carbon, undergo dehydrative Friedel–Crafts reactions upon exposure to catalytic Brønsted acid in 1,1,1,3,3,3-h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30409a3ab4c04b25120d62dd7b76a2c5
https://hal.archives-ouvertes.fr/hal-01988724/file/islandora_62906.pdf
https://hal.archives-ouvertes.fr/hal-01988724/file/islandora_62906.pdf