Results 221 to 230 of about 105,486 (290)
Enantioselective Trifunctionalization of Terminal Alkynes. [PDF]
J Am Chem SocYang L, Detels MC, Lalic G.
europepmc +1 more source
Chemistry – A European Journal, EarlyView.ABSTRACT Over the past twenty years, main group chemistry has significantly expanded its scope to include reactivities once considered the exclusive domain of transition metals. Among the emerging concepts, element‐ligand cooperation has proven to be a powerful strategy for enabling bond activation reactions but remains relatively unexplored for ...
Lennart Hensle, Viktoria H. Gessner
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Magnetic layered double hydroxide supported gold nanoparticles as a robust and recyclable catalyst for the reduction of 4- nitrophenol and oxidation of alkenes and benzyl alcohols. [PDF]
Discov NanoMavvaji M, Hosseinzadeh R, Ehsani S.
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Skeletal Editing of Alkenes with Nitroarenes via Photoinduced Rearrangement of N─O═C Dipoles Forms Lactams and Amides. [PDF]
Adv Sci (Weinh)Qin H +7 more
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Dimerization of Allylbenzenes into Cyclolignans by a Metathesis-Oxidation Sequence. [PDF]
J Org ChemVasiutovich K +3 more
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Ambient Hydrocarbonylation of Olefins Enabled by Visible-Light. [PDF]
Adv Sci (Weinh)Liu H, Zhang T, Huang H.
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General Light-Induced Pd-Catalyzed Allylic C-H Alkylation of Internal Alkenes: Direct Access to Tertiary and Quaternary Carbon Centers. [PDF]
J Am Chem SocPradhan S, Prakash G, Gevorgyan V.
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Catalytic Methods for the Transfer of Nonstabilized Carbenes. [PDF]
ACS CatalArnold ES +2 more
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2017
The α-C–H functionalization of piperidine catalyzed by tantalum complex 1 to produce amine 2 was developed (Org. Lett. 2013, 15, 2182) by Laurel L. Schafer at the University of British Columbia. An asymmetric diamination of diene 3 with diaziridine reagent 4 under palladium catalysis to furnish cyclic sulfamide 5 was developed (Org. Lett.
Allison K. Griffith, Tristan H. Lambert
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The α-C–H functionalization of piperidine catalyzed by tantalum complex 1 to produce amine 2 was developed (Org. Lett. 2013, 15, 2182) by Laurel L. Schafer at the University of British Columbia. An asymmetric diamination of diene 3 with diaziridine reagent 4 under palladium catalysis to furnish cyclic sulfamide 5 was developed (Org. Lett.
Allison K. Griffith, Tristan H. Lambert
openaire +1 more source
Chemical Reviews, 2016
Cycloadditions are among the most efficient chemical processes, combining atom economy, stereospecificity, and the ability to generate molecular complexity in a single step. Aromatic rings would in principle be ideal reaction partners, as they contain, at least from the topological point of view, both olefinic and diene subunits; however, the stability
Remy Richard, Bochet Christian G
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Cycloadditions are among the most efficient chemical processes, combining atom economy, stereospecificity, and the ability to generate molecular complexity in a single step. Aromatic rings would in principle be ideal reaction partners, as they contain, at least from the topological point of view, both olefinic and diene subunits; however, the stability
Remy Richard, Bochet Christian G
openaire +2 more sources