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作者:Franck David-Quillot , Jérôme Thibonnet ...
来源:[J].Tetrahedron Letters(IF 2.397), 2000, Vol.41 (51), pp.9981-9984
摘要:Abstract(#br)( E )-Aryl or heteroarylvinylgermanes are obtained by Stille reactions using ( E )-1-tributylstannyl-2-trialkyl (or triphenyl) germylethylenes.
作者:Franck David-Quillot , Sandrine Lunot ...
来源:[J].Tetrahedron Letters(IF 2.397), 2000, Vol.41 (25), pp.4905-4907
摘要:Abstract(#br)A simple and efficient procedure has been developed for the synthesis of organogermanium compounds by one-pot reaction of halogenogermanes, organic halides and magnesium under microwave irradiation.
作者:Franck David-Quillot , Alexia Balland ...
来源:[J].Journal of Organometallic Chemistry(IF 2), 2003, Vol.671 (1), pp.113-119
摘要:Abstract(#br)A simple and efficient procedure has been developed for the synthesis of organogermanium compounds and styrenes para -substituted with groups containing an atom of the 14th group by one-pot reaction of halogenosilanes, germanes or stannanes, organic halides and magne...
作者:Franck David-Quillot , Mohamed Abarbri
来源:[J].Tetrahedron Letters(IF 2.397), 2003, Vol.44 (8), pp.1647-1649
摘要:Abstract(#br)Using double Stille cross-coupling reaction bromo (or chloro)benzylbromide is easily transformed into substituted styrene monomers bearing a wide range of substituents in para position
作者:Franck David-Quillot , Didier Marsacq ...
来源:[J].Synthesis(IF 2.5), 2003, Vol.2003 (3), pp.0448-0454
摘要:The transfer of a β-vinylgermyl synthon is easily achievedby Stille reaction using ( E)-1-tributylstannyl-2-trialkyl(or triphenyl)germylethylenes.With this methodology good yields of ( E)-arylor heteroarylvinylgermanes, stereodefined germyldienoic acids, andgermyl α,β-enones...
作者:Franck David-Quillot , Mohamed Abarbri ...
来源:[J].Synthesis(IF 2.5), 2013, Vol.45 (5), pp.633-638
摘要:In a new synthetic approach for building systems bearing a 1,2,3-triazole moiety, we report here the first Stille cross-coupling reaction of 1,4-disubstituted 5-iodo-1,2,3-triazoles with a range of stannyl derivatives to give the corresponding 5-vinyl-1,2,3-triazoles.

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