Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Toshiaki Sasada"'
Publikováno v:
Synlett. 2011:2029-2034
The Hf(OTf)4-catalyzed unprecedented annulation of an enamine with triethyl orthoformate leading to the preparation of tetrasubstituted symmetrical pyridine derivatives without an oxidant is described. This method accommodated the single-step synthes
Publikováno v:
European Journal of Organic Chemistry. 2010:4237-4244
In the present study, we found a novel approach to the simple and practical synthesis of 3-aminopyrrole derivatives through the four-component coupling reaction of a functionalized silane, a nitrile, an aldehyde, and trimethylsilyl cyanide by Yb(OTf)
Publikováno v:
European Journal of Organic Chemistry. 2009:5738-5743
An unprecedented three-component coupling reaction was developed for the synthesis of 3,4-fused pyrimidin-2-one and pyrimidin-2-thione derivatives from an α-acidic imine compound, a nitrile, and triphosgene or carbon disulfide. This method can be us
Publikováno v:
ChemInform. 43
The [5+1] annulation of enamidines, which were prepared from functionalized silanes, organolithium compounds and two nitriles, with N,N-dimethylformamide dialkyl acetals as the C1 unit is described, leading to the synthesis of tri- and tetrasubstitut
Publikováno v:
ChemInform. 43
An unprecedented annulation of enamines with triethyl orthoformate allows the preparation of tetrasubstituted pyridines.
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 17(34)
The [5+1] annulation of enamidines, which were prepared from functionalized silanes, organolithium compounds and two nitriles, with N,N-dimethylformamide dialkyl acetals as the C1 unit is described, leading to the synthesis of tri- and tetrasubstitut
Publikováno v:
ChemInform. 41
In addition to the novel synthesis of 3-aminopyrroles, the transformation of pyrroles bearing the isoxazole group into pyrrolo[3,4-b]pyridin-4-ones through a reductive ring-opening reaction and subsequent intramolecular cyclization is reported.
Publikováno v:
ChemInform. 41
An unprecedented three-component coupling reaction was developed for the synthesis of 3,4-fused pyrimidin-2-one and pyrimidin-2-thione derivatives from an α-acidic imine compound, a nitrile, and triphosgene or carbon disulfide. This method can be us
Publikováno v:
ChemInform. 40
We have identified a Me3SiCl-mediated three-component coupling reaction of a functionalized enamine, N,N-dimethylformamide diethyl acetal, and an internal alkyne having an electron-withdrawing group that produces 2,3,4,5-tetrasubstituted pyridine der
Publikováno v:
The Journal of organic chemistry. 73(17)
We have identified a Me3SiCl-mediated three-component coupling reaction of a functionalized enamine, N,N-dimethylformamide diethyl acetal, and an internal alkyne having an electron-withdrawing group that produces 2,3,4,5-tetrasubstituted pyridine der