Zobrazeno 1 - 10
of 73
pro vyhledávání: '"Fabien Boeda"'
Publikováno v:
SynOpen, Vol 02, Iss 01, Pp 0041-0049 (2018)
Abstract The titanium-catalyzed asymmetric cyclopropanation of cyanoesters with Grignard reagents was investigated for the first time. Particularly, the study of the efficiency of Taddol-based titanium complexes has shown that the prior preparati
Externí odkaz:
https://doaj.org/article/57eac40f7d6c43efae980f840200ffce
Autor:
Meng Liu, Nejib Dwadnia, Tony Chevalier, Annie Hemon‐Ribaud, Morwenna S. M. Pearson‐Long, Fabien Boeda, Philippe Bertus
Publikováno v:
European Journal of Organic Chemistry. 2022
Autor:
Fabien Boeda, Laurent Fontaine, Mathilde Pantin, Philippe Bertus, M. S. M. Pearson-Long, Julien Caillé
Publikováno v:
European Journal of Organic Chemistry. 2019:7359-7366
Autor:
Fabien Boeda, Jordan Saillour, Mathilde Pantin, M. S. M. Pearson-Long, Philippe Bertus, Florent Bodinier, Yassine M. Youssouf
Publikováno v:
Tetrahedron
Tetrahedron, Elsevier, 2019, 75 (33), pp.4657-4662. ⟨10.1016/j.tet.2019.07.010⟩
Tetrahedron, Elsevier, 2019, 75 (33), pp.4657-4662. ⟨10.1016/j.tet.2019.07.010⟩
International audience; A convenient access to 2-hydroxycyclopentenones was designed from acylcyanohydrins, byusing titanacyclopropane complexes as nucleophilic partners and an intramolecular aldolcondensation in basic conditions. The development of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6fa4508ef034ba57e7b1892370478bb
https://hal.archives-ouvertes.fr/hal-02312591/document
https://hal.archives-ouvertes.fr/hal-02312591/document
Publikováno v:
SYNTHESIS
SYNTHESIS, Georg Thieme Verlag, 2019, 51 (06), pp.1329-1341. ⟨10.1055/s-0037-1611704⟩
SYNTHESIS, Georg Thieme Verlag, 2019, 51 (06), pp.1329-1341. ⟨10.1055/s-0037-1611704⟩
International audience; Allylzinc reagents were used to access highly functionalized tertiary carbinamine derivatives in high yields from cyanoesters and cyanocarbonates. While the monoaddition of organometallics on nitriles is generally observed, in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea06229ccf55110bad0c483e69ea45a5
https://hal.archives-ouvertes.fr/hal-02132643
https://hal.archives-ouvertes.fr/hal-02132643
Autor:
Florian Rouzier, Fabien Boeda, Julien Caillé, Philippe Bertus, Morwenna S. M. Pearson-Long, Houcine Ammar, Fatma Boukattaya
Publikováno v:
SYNTHESIS
SYNTHESIS, Georg Thieme Verlag, 2016, 48 (06), pp.906-916. ⟨10.1055/s-0035-1560404⟩
SYNTHESIS, Georg Thieme Verlag, 2016, 48 (06), pp.906-916. ⟨10.1055/s-0035-1560404⟩
International audience; A straightforward synthesis of symmetrically α,α-disubstituted α-amino acids is presented. The key step of this process relies on the efficient double addition of Grignard reagents to acyl cyanohydrins to provide N-acyl ami
Autor:
Fatma Boukattaya, Fabien Boeda, Philippe Bertus, Neji Gharsallah, Adel Kadri, M. S. M. Pearson-Long, Houcine Ammar, Amal Daoud
Publikováno v:
Medicinal Chemistry
Medicinal Chemistry, Bentham Science Publishers, 2018, 14, ⟨10.2174/1573406414666181009124449⟩
Medicinal Chemistry, Bentham Science Publishers, 2018, 14, ⟨10.2174/1573406414666181009124449⟩
Background: 2-Aminochromene derivatives display important pharmacological properties, including mainly antibiotic and anticancer activities. Objective: The study aims to synthesize new chromene derivatives via a new approach using Grignard reagents,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::225cbaaf054b353fa69647a726b14ff8
https://hal-univ-lemans.archives-ouvertes.fr/hal-01921815
https://hal-univ-lemans.archives-ouvertes.fr/hal-01921815
Publikováno v:
SynOpen
SynOpen, 2018, 02 (01), pp.0041-0049. ⟨10.1055/s-0036-1591933⟩
SynOpen, Vol 02, Iss 01, Pp 0041-0049 (2018)
SynOpen, 2018, 02 (01), pp.0041-0049. ⟨10.1055/s-0036-1591933⟩
SynOpen, Vol 02, Iss 01, Pp 0041-0049 (2018)
International audience; The titanium-catalyzed asymmetric cyclopropanation of cyanoesters with Grignard reagents was investigated for the first time. Particularly, the study of the efficiency of Taddol-based titanium complexes has shown that the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0acfc3506ff72c5f5e9f8f9c58dec4d2
https://hal.archives-ouvertes.fr/hal-02132515
https://hal.archives-ouvertes.fr/hal-02132515
Autor:
Fabien Boeda, Julien Caillé, Houcine Ammar, M. S. M. Pearson-Long, Philippe Bertus, Fatma Boukattaya
Publikováno v:
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2018, 16 (9), pp.1519-1526. ⟨10.1039/c7ob03047a⟩
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2018, 16 (9), pp.1519-1526. ⟨10.1039/c7ob03047a⟩
International audience; The successive addition of two different Grignard reagents to acyl cyanohydrins was performed with success by taking advantage of the low reactivity of alkynyl Grignard reagents. The experimental conditions were adjusted so th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54575339be909f2ee96bc32d124a0c61
https://hal-univ-lemans.archives-ouvertes.fr/hal-01914744
https://hal-univ-lemans.archives-ouvertes.fr/hal-01914744
Publikováno v:
Advanced Synthesis and Catalysis
Advanced Synthesis and Catalysis, Wiley-VCH Verlag, 2017, 359 (2), pp.179-201. ⟨10.1002/adsc.201600727⟩
Advanced Synthesis and Catalysis, Wiley-VCH Verlag, 2017, 359 (2), pp.179-201. ⟨10.1002/adsc.201600727⟩
International audience; As depicted in many textbooks, the addition of organometallics to nitriles is generally limited to a single addition, providing ketones after acidic hydrolysis. However, the double addition, leading to tertiary carbinamines is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2db9d2659d8dc15d2d878e0327c2d68e
https://hal-univ-lemans.archives-ouvertes.fr/hal-01914752
https://hal-univ-lemans.archives-ouvertes.fr/hal-01914752