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Decorating and diversifying drugs
Asymmetric C(sp2)-H Activation
Diastereoselective Substrate-Controlled Transition Metal-Catalyzed C-H Activation: An Old Solution to a Modern Synthetic Challenge
High-Yielding, Versatile, and Practical [Rh(III)Cp*]-Catalyzed Ortho Bromination and Iodination of Arenes
C-H bond activation enables the rapid construction and late-stage diversification of functional molecules
Rh(III)- and Ir(III)-Catalyzed C–C Bond Cross Couplings from C–H Bonds
Highlights from the 54th EUCHEM Bürgenstock Conference on Stereochemistry, Brunnen, Switzerland, May 2019
Cyclometallated complexes as catalysts for C–H activation and functionalization
Challenging Atroposelective C–H Arylation
Highly Efficient Synthesis of Hindered 3-Azoindoles via Metal-Free C–H Functionalization of Indoles
Towards mild metal-catalyzed C-H bond activation
Beyond Directing Groups: Transition-Metal-Catalyzed C-H Activation of Simple Arenes
Rhodium(III) and Hexabromobenzene-A Catalyst System for the Cross-Dehydrogenative Coupling of Simple Arenes and Heterocycles with Arenes Bearing Directing Groups
Enantioselective 1,4-conjugate addition of diethylzinc to (E)-alkenyl aryl ketones catalysed by Cu/DiPPAM complex
[RhIIICp*]-Catalyzed Dehydrogenative Aryl?Aryl Bond Formation
Super-reactive catalyst for bond cleavage
Regiodivergent Visible Light-Induced C–H Functionalization of Quinolines at C-5 and C-8 under Metal-, Photosensitizer- and Oxidant-Free Conditions
Asymmetric C–H activation as a modern strategy towards expedient synthesis of steganone

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