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Efficient and Complementary Methods Offering Access to Synthetically Valuable 1,2-Dibromobenzenes
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
The Effect of Sulfoxides on the Stereoselective Construction of Tetrahydrofurans: Total Synthesis of (+)-Goniothalesdiol
Stereoselective Synthesis of 2H-Chromans by Reductive Deoxygenation of Differently Substituted 2-Sulfinylmethylchroman-2-ols
Catalytic Palladium Phosphination: Modular Synthesis of C-1-Symmetric Biaryl-Based Diphosphines
Diastereoselective Substrate-Controlled Transition Metal-Catalyzed C-H Activation: An Old Solution to a Modern Synthetic Challenge
Asymmetric C(sp2)-H Activation
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
Construction of the biaryl-part of vancomycin aglycon via atropo-diastereoselective Suzuki-Miyaura coupling
Regioselectivity in the Aryne Cross-Coupling of Aryllithiums with Functionalized 1,2-Dibromobenzenes
Through-Space J(P,P) and J(P,F) Spin-Spin Coupling in C-1-Symmetric Biaryl Diphosphanes
Palladium-Catalyzed Intramolecular Direct Arylation of 2-Bromo-diaryl Sulfoxides via C-H Bond Activation
Stereoselective Synthesis of P-Chirogenic Dibenzophosphole-Boranes via Aryne Intermediates
Stereoselective synthesis of the C15-C26 fragment of the antitumor agent (-)-Dictyostatin
Recent advances in the diastereoselective Reformatsky-type reaction
Transition-Metal-Free Atropo-Selective Synthesis of Biaryl Compounds Based on Arynes

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