Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Erwann Grenet"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 1208-1214 (2018)
The C–H indolation of heteroarenes was realized using the benziodoxolone hypervalent iodine reagents indoleBXs. Functionalization of the C–H bond in bipyridinones and quinoline N-oxides catalyzed by a rhodium complex allowed to incorporate indole
Externí odkaz:
https://doaj.org/article/9b112c380968457c834e90c91f96a627
Publikováno v:
Synthesis. 55:580-597
Activated dienones bearing a chiral sulfoxide were transformed diastereodivergently into the corresponding disubstituted 3,4,5,6-tetrahydrocyclopenta[b]pyran-7(2H)-ones. The torquoselectivity of the reaction could be switched by changing the Lewis ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa0bf9f3f4bd843197e4fb5c7c712dc4
https://doi.org/10.1055/a-1983-2140
https://doi.org/10.1055/a-1983-2140
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2021, 23 (21), pp.8539-8542. ⟨10.1021/acs.orglett.1c03237⟩
Organic Letters, American Chemical Society, 2021, 23 (21), pp.8539-8542. ⟨10.1021/acs.orglett.1c03237⟩
Crystallization-Induced Diastereomer Transformation (CIDT) of α-bromo-α'-(R)-sulfinylketones is reported. This process provides not readily accessible enantiopure stereolabile α-bromoketones, which after diastereoselective carbonyl group reduction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9618799b79adb7189b6de2f2a6126cd5
https://doi.org/10.1021/acs.orglett.1c03237
https://doi.org/10.1021/acs.orglett.1c03237
Publikováno v:
European Journal of Organic Chemistry. 2022
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e53534fd01aaa098413f2ffb27037efc
https://doi.org/10.1002/ejoc.202200828
https://doi.org/10.1002/ejoc.202200828
Publikováno v:
Asian Journal of Organic Chemistry
Asian Journal of Organic Chemistry, Wiley, 2017, 6 (2), pp.189-198. ⟨10.1002/ajoc.201600471⟩
Asian Journal of Organic Chemistry, Wiley, 2017, 6 (2), pp.189-198. ⟨10.1002/ajoc.201600471⟩
In this study we describe a Nazarov cyclization of activated dienones bearing an aromatic moiety as EDG and a chiral sulfoxide group both as an EWG and a chiral inductor. The sulfinyl group directed the torquoselectivity, and AlCl3 was used as a prom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4119a1797401df522d2681b498d49f8
https://doi.org/10.1002/ajoc.201600471
https://doi.org/10.1002/ajoc.201600471
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 1208-1214 (2018)
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 1208-1214 (2018)
The C–H indolation of heteroarenes was realized using the benziodoxolone hypervalent iodine reagents indoleBXs. Functionalization of the C–H bond in bipyridinones and quinoline N-oxides catalyzed by a rhodium complex allowed to incorporate indole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9120f951e124c8b192890d6f3ed3609
https://pubmed.ncbi.nlm.nih.gov/29977388
https://pubmed.ncbi.nlm.nih.gov/29977388
Autor:
Erwann Grenet, Jerome Waser
The C-H heteroarylation of benzaldehydes with indoles and pyrroles was realized using the benziodoxolone hypervalent iodine reagents indole- and pyrroleBX. Functionalization of the aldehyde C-H bond using either an o-hydroxy or amino directing group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0769bac4bf81005a4f89137997c1be4f
https://infoscience.epfl.ch/record/256007
https://infoscience.epfl.ch/record/256007
Autor:
Grenet, Erwann1 (AUTHOR), Robidas, Raphaël2 (AUTHOR), van der Lee, Arie3 (AUTHOR), Legault, Claude Y.2 (AUTHOR) claude.legault@usherbrooke.ca, Salom‐Roig, Xavier J.1 (AUTHOR) Xavier.Salom-Roig@umontpellier.fr
Publikováno v:
European Journal of Organic Chemistry. 9/27/2022, Vol. 2022 Issue 36, p1-7. 7p.
Publikováno v:
Chemistry - A European Journal. 2/26/2019, Vol. 25 Issue 12, p3010-3013. 4p.
Publikováno v:
Synthesis; Feb2023, Vol. 55 Issue 4, p580-597, 18p