Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Yun-Long Wei"'
Publikováno v:
Synlett. 31:21-34
The organosilicon-mediated organic synthesis (SiMOS) has attracted much attention over the recent decades. However, the use of organosilicon reagents with novel catalytic strategies remains to be explored. This Account summarizes our group’s progre
Autor:
Yun-Long Wei1, Yajun Ren1, Mailhol, Damien1, Rajzmann, Michel1, Rodriguez, Jean1 jean.rodriguez@univ-amu.fr, Coquerel, Yoann1 yoann.coquerel@univ-amu.fr
Publikováno v:
Advanced Synthesis & Catalysis. 6/18/2019, Vol. 361 Issue 12, p1-11. 11p.
Publikováno v:
Advanced Synthesis and Catalysis
Advanced Synthesis and Catalysis, Wiley-VCH Verlag, 2019, 361, pp.2992-3001. ⟨10.1002/adsc.201900159⟩
Advanced Synthesis and Catalysis, 2019, 361, pp.2992-3001. ⟨10.1002/adsc.201900159⟩
Advanced Synthesis and Catalysis, Wiley-VCH Verlag, 2019, 361, pp.2992-3001. ⟨10.1002/adsc.201900159⟩
Advanced Synthesis and Catalysis, 2019, 361, pp.2992-3001. ⟨10.1002/adsc.201900159⟩
International audience; An original two-step organocatalytic syn- thesis of optically active glutarimides from 2- oxocyclobutane carboxamides is described featuring an isothiourea-catalyzed two-atom ring-expansive rearrangement.
Publikováno v:
Chemical Communications. 55:5922-5925
We describe a photocatalyzed transformation for the synthesis of the indolo[2,1-a]isoquinoline core structure. This redox neutral reaction features mild reaction conditions and exceptional functional group tolerance. A series of valuable indolo[2,1-a
Publikováno v:
Journal of the American Chemical Society
Journal of the American Chemical Society, American Chemical Society, 2020, 142 (40), pp.16921-16925. ⟨10.1021/jacs.0c08218⟩
Journal of the American Chemical Society, 2020, 142 (40), pp.16921-16925. ⟨10.1021/jacs.0c08218⟩
Journal of the American Chemical Society, American Chemical Society, 2020, 142 (40), pp.16921-16925. ⟨10.1021/jacs.0c08218⟩
Journal of the American Chemical Society, 2020, 142 (40), pp.16921-16925. ⟨10.1021/jacs.0c08218⟩
International audience; Enantioenriched aryne atropisomers having a biaryl stereogenic axis vicinal to the reactive triple bond are demonstrated to exist. These reaction intermediates are easily produced in situ and can undergo the standard aryne cyc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e7ceead7f889a1bb0e76c35d603a798
https://hal.archives-ouvertes.fr/hal-02990635
https://hal.archives-ouvertes.fr/hal-02990635
Publikováno v:
Applied Mechanics and Materials. 868:236-241
In this paper, graphene nanosuspension was spray deposited using electrohydrodynamic atomization (EHDA) technique, and the polydimethylsiloxane (PDMS) was used as the substrate during the EHDA process. The effect of the PDMS substrate before and afte
Publikováno v:
Angewandte Chemie International Edition
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2019, 58 (2), pp.456-460. ⟨10.1002/anie.201810184⟩
Angewandte Chemie International Edition, 2019, 58 (2), pp.456-460. ⟨10.1002/anie.201810184⟩
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2019, 58 (2), pp.456-460. ⟨10.1002/anie.201810184⟩
Angewandte Chemie International Edition, 2019, 58 (2), pp.456-460. ⟨10.1002/anie.201810184⟩
International audience; An enantioselective Michael addition-four-atom ring expansion cascade reaction involving cyclobutanones activated by a N-aryl secondary amide group and ortho-amino nitrostyrenes has been developed for the preparation of functi
Publikováno v:
Chemical Communications. 52:6455-6458
The intramolecular 1,5-H transfer reaction of the aryl radicals generated from unactivated aryl iodides by photocatalysis is described. The features of this transformation are operational simplicity, excellent yields, mild reaction conditions, and go
Publikováno v:
Chemical communications (Cambridge, England). 54(16)
A novel strategy involving visible-light-induced functionalization of alkenes for the synthesis of substituted aziridines was developed. The readily prepared N-protected 1-aminopyridinium salts were used for the generation of N-centered radicals. Thi
Publikováno v:
The Journal of organic chemistry. 83(1)
The decarbonylation of primary, secondary, and tertiary alkyl-substituted acyl radicals has been investigated through photoredox catalysis. A series of quaternary carbons and γ-ketoesters have been directly constructed by the photoredox 1,4-conjugat