Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Vincent Pirenne"'
Publikováno v:
Angewandte Chemie.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64fa28e21d2027f4dde47b1847d1b8a2
https://doi.org/10.1002/ange.202302420
https://doi.org/10.1002/ange.202302420
Publikováno v:
Best Practice & Research Clinical Anaesthesiology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8c24e25877feff843eab742c2a3ee79
https://doi.org/10.1016/j.bpa.2023.03.006
https://doi.org/10.1016/j.bpa.2023.03.006
Publikováno v:
Chemical Reviews. 121:227-263
This review describes the development of enantioselective methods for the ring opening of cyclopropanes. Both approaches based on the reaction of nonchiral cyclopropanes and (dynamic) kinetic resolutions and asymmetric transformations of chiral subst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d6d58e1310c463769d9d959d98be5dd
https://doi.org/10.1021/acs.chemrev.0c00109
https://doi.org/10.1021/acs.chemrev.0c00109
Publikováno v:
Chemistry – A European Journal. 28
The total enantioselective synthesis of (+)-eucophylline 1 was achieved using as a key-structural motif a chiral piperidinone bearing the natural product all-carbon quaternary stereocenter. The elaboration of the latter is based on two strategies rel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::775f88a9c5c069f6f183a9b2094b96f2
https://doi.org/10.1002/chem.202200088
https://doi.org/10.1002/chem.202200088
Publikováno v:
Chemical Science
The efficient catalytic activation of donor–acceptor aminocyclopropanes lacking the commonly used diester acceptor is reported here in a (3 + 2) dearomative annulation with indoles. Bench-stable tosyl-protected aminocyclopropyl esters were converte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b993d8efdac02ea2d860263cada79c7f
https://doi.org/10.1039/d1sc01127h
https://doi.org/10.1039/d1sc01127h
Autor:
Jonathan Lusseau, Yannick Landais, Dario M. Bassani, Iman Traboulsi, Lisa Rouvière, Stéphane Massip, Vincent Pirenne, Frédéric Robert
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2020, 22 (2), pp.575-579. ⟨10.1021/acs.orglett.9b04345⟩
Organic Letters, American Chemical Society, 2020, 22 (2), pp.575-579. ⟨10.1021/acs.orglett.9b04345⟩
The photosensitized p-anisaldehyde-mediated addition of sulfonylcyanides onto the π-system of cyclobutenes is shown to afford highly functionalized cyclobutanes in high yields and diastereocontrol. The homochiral cyclobutene precursors are accessibl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c07fda15b4f8ef6604c18527e2087d66
https://hal.archives-ouvertes.fr/hal-02499993/document
https://hal.archives-ouvertes.fr/hal-02499993/document
Autor:
Chahinaz Khiar, Vincent Pirenne, Haitham Hassan, Frédéric Robert, Ashique Hussain, Yannick Landais, Maren Wissing
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2017, 23 (19), pp.4651-4658. ⟨10.1002/chem.201605946⟩
Chemistry-A European Journal, Wiley-VCH Verlag, 2017, 23 (19), pp.4651-4658. ⟨10.1002/chem.201605946⟩
International audience; The free-radical three-component carbocyanation of electron-rich olefins was investigated with p-tosyl cyanide as cyanide source. The scope and limitations of the process were established by varying the nature of the alkene an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78556a257d0234e878fd0f1775c66b2a
https://hal-pasteur.archives-ouvertes.fr/pasteur-03033282
https://hal-pasteur.archives-ouvertes.fr/pasteur-03033282