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Highly Efficient One-Pot Access to Functionalized Arylboronic Acids via Noncryogenic Bromine/Magnesium Exchanges
Bromine-lithium exchange: An efficient tool in the modular construction of biaryl ligands
Highly Efficient One-Pot Access to Functionalized Arylboronic Acids via Noncryogenic Bromine/Magnesium Exchanges
Efficient and Complementary Methods Offering Access to Synthetically Valuable 1,2-Dibromobenzenes
Super-reactive catalyst for bond cleavage
C-H Activation for Asymmetric Synthesis
Construction of the biaryl-part of vancomycin aglycon via atropo-diastereoselective Suzuki-Miyaura coupling
Aryne-mediated fluorination: Synthesis of fluorinated biaryls via a sequential desilylation-halide elimination-fluoride addition process
Atropodiastereoselective C-H Olefination of Biphenyl p-Tolyl Sulfoxides with Acrylates
Efficient palladium catalyzed synthesis of heteroaromatic sulfoxides
Atroposelective arylation of biaryls by C-H activation
Synthesis and biological evaluation of new nucleosides derived from trifluoromethoxy-4-quinolones
Catalytic Palladium Phosphination: Modular Synthesis of C-1-Symmetric Biaryl-Based Diphosphines
Atroposelective synthesis of axially chiral P,S-ligands based on arynes
Through-Space J(P,P) and J(P,F) Spin-Spin Coupling in C-1-Symmetric Biaryl Diphosphanes
Visible-Light-Triggered, Metal- and Photocatalyst-Free Acylation of N-Heterocycles
Regioselectivity in the Aryne Cross-Coupling of Aryllithiums with Functionalized 1,2-Dibromobenzenes
Stereoselective Synthesis of P-Chirogenic Dibenzophosphole-Boranes via Aryne Intermediates
Stereoselective Sulfinyl Aniline-Promoted Pd-Catalyzed C−H Arylation and Acetoxylation of Aliphatic Amides
Transition-Metal-Free Atropo-Selective Synthesis of Biaryl Compounds Based on Arynes

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