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Experimental and DFT study on the indiummediated synthesis of benzophenones via arylstannanes
(Royal Society of Chemistry, 2014-09)
Experimental results of the solvent-free, indium-promoted reaction of aroyl chlorides with arylstannanes showed a narrow scope; its efficiency depends both on the extent of methylation in the latter and on the nature, ...
Selective synthetic routes to sterically hindered unsymmetrical diaryl ketones via arylstannanes
(American Chemical Society, 2011-03)
Bulky arylstannanes and bulky aroyl chlorides are good reaction partners for the synthesis of two-, three-, and even four-ortho-substituted benzophenones, in good to excellent isolated yields (47-91%). Three simple and ...
Indium-mediated regioselective synthesis of ketones from arylstannanes under solvent-free ultrasound irradiation
(Elsevier, 2013-05)
The solvent-free indium-promoted reaction of alkanoyl chlorides with sterically and electronically diverse arylstannanes is a simple and direct method for the regioselective synthesis of primary, secondary and tertiary ...
Ultrasound-assisted synthesis of benzophenones by Stille cross-coupling reactions. Optimization via experimental design
(Elsevier, 2013-01-01)
A series of diaryl ketones have been synthesized in moderate to excellent yields through the selective cross-coupling reaction of benzoyl chlorides with arylstannanes using a sonochemical variation of the Stille coupling. ...
tri-n-butyltin hydride-mediated radical reaction of a 2-iodobenzamide: Formation of an unexpected carbon-tin bond
(Sociedade Brasileira de Química, 2008)
Strategies for the synthesis of bi- and triarylic materials starting from commercially available phenols
(Elsevier Science Sa, 2005)
tri-n-butyltin hydride-mediated radical reaction of a 2-iodobenzamide: formation of an unexpected carbon-tin bond
(Sociedade Brasileira de Química, 2007)