Zobrazeno 1 - 10
of 90
pro vyhledávání: '"Beatrice Quiclet‐Sire"'
Autor:
Beatrice Quiclet‐Sire, Samir Z. Zard
Publikováno v:
SYNLETT
SYNLETT, Georg Thieme Verlag, 2016, 27 (5), pp.680-701. ⟨10.1055/s-0035-1561300⟩
SYNLETT, Georg Thieme Verlag, 2016, 27 (5), pp.680-701. ⟨10.1055/s-0035-1561300⟩
An overview of a convergent, modular route to protected amines, anilines, and related compounds hinging on the degenerate radical addition-transfer of xanthates is presented. Emphasis is placed on the importance of the stabilization of the starting r
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2013, 15 (24), pp.6250-6253. ⟨10.1021/ol403103u⟩
Organic Letters, American Chemical Society, 2013, 15 (24), pp.6250-6253. ⟨10.1021/ol403103u⟩
International audience; 2-Fluoropyridinyl-6-oxy- precursors derived from phenyl vinyl sulfide react with radicals generated from xanthates via an addition-elimination process to furnish the corresponding vinyl sulfides in good yields. This convergent
Autor:
Beatrice Quiclet‐Sire, Samir Z. Zard
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2013, 15 (22), pp.5886-5889. ⟨10.1021/ol402973q⟩
Organic Letters, American Chemical Society, 2013, 15 (22), pp.5886-5889. ⟨10.1021/ol402973q⟩
International audience; Upon heating at 180-200 °C in diphenyl ether, S-(4-oximinoalkyl)xanthates with a secondary isopropyl or isobutyl group on the oxygen undergo a Chugaev elimination followed by ring closure onto the oxime to give dihydrothiazin
Autor:
Samir Z. Zard, Beatrice Quiclet‐Sire
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Beilstein-Institut, 2013, 9, pp.557-576. ⟨10.3762/bjoc.9.61⟩
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 557-576 (2013)
Beilstein Journal of Organic Chemistry, Beilstein-Institut, 2013, 9, pp.557-576. ⟨10.3762/bjoc.9.61⟩
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 557-576 (2013)
International audience; This review article describes briefly some of the radical processes developed in the authors' laboratory as they pertain to the concise assembly of complex molecular scaffolds. The emphasis is placed on the use of nitrogen-cen
Autor:
Samir Z. Zard, Beatrice Quiclet‐Sire
Publikováno v:
ChemInform. 47
An overview of a convergent, modular route to protected amines, anilines, and related compounds hinging on the degenerate radical addition-transfer of xanthates is presented. Emphasis is placed on the importance of the stabilization of the starting r
Autor:
Beatrice Quiclet‐Sire, Samir Z. Zard
Publikováno v:
Pure and Applied Chemistry
Pure and Applied Chemistry, De Gruyter, 2011, 83 (3), pp.519-551. ⟨10.1351/pac-con-10-08-07⟩
Pure and Applied Chemistry, De Gruyter, 2011, 83 (3), pp.519-551. ⟨10.1351/pac-con-10-08-07⟩
International audience; The degenerative radical addition-transfer of xanthates onto alkenes allows the rapid assembly of richly functionalized structures. Various families of open-chain, cyclic, and polycyclic compounds can thus be readily accessed.
Autor:
Samir Z. Zard, Beatrice Quiclet‐Sire
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2008, 10 (15), pp.3279-82. ⟨10.1021/ol801162m⟩
Organic Letters, American Chemical Society, 2008, 10 (15), pp.3279-82. ⟨10.1021/ol801162m⟩
International audience; S-Succinimidomethyl- and S-phthalimidomethyl xanthates are added efficiently to various alkenes resulting in an overall aminomethylation process. In contrast, under similar conditions, S-pyrrolidonyl xanthate gives rise mostly
Publikováno v:
Tetrahedron
Tetrahedron, Elsevier, 2007, 63 (30), pp.7187-7212. ⟨10.1016/j.tet.2007.04.091⟩
Tetrahedron, Elsevier, 2007, 63 (30), pp.7187-7212. ⟨10.1016/j.tet.2007.04.091⟩
A route to 3-arylpiperidines and 3-arylpyrrolidines involving radical 1,4- and 1,2-aryl migrations has been explored. For the piperidines, the first route requires a xanthate addition to an N-allylarylsulfonamide, followed by acetylation and treatmen
Publikováno v:
ChemInform. 46
ConspectusRadical allylations represent effective routes to various alkenes, but to date they have relied chiefly on organostannane derivatives and still suffer from significant limitations with respect to the substitution pattern of the starting all
Publikováno v:
Angewandte Chemie International Edition
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2006, 45 (30), pp.5002-5006. ⟨10.1002/anie.200601556⟩
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2006, 45 (30), pp.5002-5006. ⟨10.1002/anie.200601556⟩
International audience; (Chemical Equation Presented) Radically useful: The radical addition of dithiocarbonates to branched allyl diphenylphosphine oxides can be followed by elimination of a diphenylphosphinoyl radical, thereby giving rise to allyla