Trimethylsilyl-substituted cyclopentadienes
نویسندگان
چکیده
منابع مشابه
Nickel-catalyzed decarbonylative alkylidenation of phthalimides with trimethylsilyl-substituted alkynes.
We have developed a nickel-catalyzed transformation, in which phthalimides react with trimethylsilyl-substituted alkynes in the presence of Ni(0)/PMe3/MAD catalyst to provide isoindolinones. The reaction process displays an unusual mechanistic feature-decarbonylation and alkylidenation. The use of both trimethylsilyl-substiuted alkynes and MAD was found to be essential for the transformation wi...
متن کاملDiradical reaction mechanisms in [3 + 2]-cycloadditions of hetaryl thioketones with alkyl- or trimethylsilyl-substituted diazomethanes
Reactions of dihetaryl and aryl/hetaryl thioketones with 2-diazopropane, diazoethane, and (trimethylsilyl)diazomethane were studied at variable temperature. The experiments showed that reactions with 2-diazopropane carried out at -75 °C occur mainly via the initially formed, relatively stable 1,3,4-thiadiazolines as products of the [3 + 2]-cycloaddition of the diazo dipole onto the C=S bond. Th...
متن کاملSolid state structures and photophysical properties of (trimethylsilyl)methyl-substituted anthracenes and pyrenes.
(Trimethylsilyl)methyl groups incorporated at 9- and 9,10-positions of anthracenes and at 1,3,6,8-positions of pyrenes were found to orient perpendicular to the aromatic frameworks in their crystals and induce red-shift of UV absorption and fluorescence spectra and enhancement of fluorescence quantum yields as compared with the parent hydrocarbons.
متن کاملFacile two-step synthesis of 3-substituted indazoles using diazo(trimethylsilyl)methylmagnesium bromide.
Diazo(trimethylsilyl)methylmagnesium bromide readily reacted with various ketones and aldehydes to give the corresponding 2-diazo-(2-trimethylsilyl)ethanols. These were efficiently converted to indazoles bearing hydroxymethyl units at the 3-position by intermolecular [3 + 2] cycloaddition with benzynes.
متن کاملGold(I)-catalyzed synthesis of functionalized cyclopentadienes.
mechanistic pathways: a concerted rearrangement (path a) involving direct addition of the olefin on the epoxide or a stepwise mechanism (path b) through a Nazarov cyclization of an oxypentadienyl cation (2, X=O ). The regioselectivity of the cyclization is dictated by donation of the oxyanion into the resulting cation leading to the formation of a ketone. Recently, stabilization of developing p...
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ژورنال
عنوان ژورنال: Canadian Journal of Chemistry
سال: 1970
ISSN: 0008-4042,1480-3291
DOI: 10.1139/v70-525