Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Rodrigo Webber"'
Autor:
Muhammad I. Qadir, Marta Martín, Eduardo Sola, Jairton Dupont, Rodrigo Webber, Elizabeth Suárez
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Catalysis Communications
instname
Catalysis Communications
Complex [IrClH{κP,P,Si-Si(Me)(C6H4–2-PiPr2)2}] (1) showed a remarkable catalytic activity for CO2 hydrogenation in a DMSO/H2O solvent system incorporating 1,2-dimethyl-3-butylimidazolium acetate ionic liquid (IL), producing 0.94 M formic acid with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebf5c68c0a033b2e87e8d38b65a714c4
http://hdl.handle.net/10261/233103
http://hdl.handle.net/10261/233103
The reduction of carbon dioxide (CO2) has become one of the main goals needed to overcome global warming. The transformation of CO2 into chemicals and fuels (formic acid, methanol, methane, and higher hydrocarbons) can be a resource and provide an en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d4559703dace822114dc7952a0819d7
https://doi.org/10.1016/bs.adomc.2019.02.005
https://doi.org/10.1016/bs.adomc.2019.02.005
Autor:
Angelita M. Barcellos, Patrick C. Nobre, Gelson Perin, Thiago J. Peglow, Ricardo F. Schumacher, Juliano A. Roehrs, Rodrigo Webber
Publikováno v:
ChemInform. 47
We describe here a metal-free and selective method for the synthesis of (E)-1-bromo-1-seleno alkenes and ketene selenoacetals by a stoichiometric and temperature-controlled reaction. These protocols employ a diverse array of 1,1-dibromoalkenes and di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54355eb7e17c81dd520d2de4603cbbb1
https://doi.org/10.1002/chin.201652381
https://doi.org/10.1002/chin.201652381
Autor:
Eder João Lenardão, Raquel G. Jacob, Katiúcia D. Mesquita, Renata G. Lara, Rodrigo Webber, Débora Martins Martinez, Lucielli Savegnago, Samuel R. Mendes, Diego Alves, Gelson Perin
Publikováno v:
Green Chemistry Letters and Reviews. 6:269-276
We describe herein the use of glycerol as an efficient and recyclable solvent for the addition of thiols to nonactivated alkenes. The catalyst-free reactions take place easily using glycerol at room temperature or heating and the corresponding linear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5caa56a7222c14c67cb3438106f32274
https://doi.org/10.1080/17518253.2013.811298
https://doi.org/10.1080/17518253.2013.811298
Publikováno v:
Proceedings of the 15th Brazilian Meeting on Organic Synthesis Proceedings.
Organoselenium compounds are attractive synthetic targets because of their interesting biological activities as antioxidant 1 and antifungal. 2 Among organochalcogen compounds, the divinylic selenides and tellurides play an important role in organic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::efd80f5f8de9bd8155bcb2f1a1587335
https://doi.org/10.5151/chempro-15bmos-bmos2013_2013820175049
https://doi.org/10.5151/chempro-15bmos-bmos2013_2013820175049
Publikováno v:
ChemInform. 44
The reagent system is employed for the in situ generation of organylselenols which react further with 2-chloropyridines.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb044f92bc5b58bef8c27360168f240a
https://doi.org/10.1002/chin.201339151
https://doi.org/10.1002/chin.201339151
Publikováno v:
Tetrahedron Letters. (24):3215-3218
We describe herein an efficient and simple method to synthesize 2-organylselanyl pyridines by reactions of 2-chloropyridines with organylselenols, generated in situ by reaction of diorganyl diselenides, using glycerol as solvent and hypophosphorous a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa5c076682f7bf31ad8ba25335bf7c55