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Super-reactive catalyst for bond cleavage
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
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
Atroposelective arylation of biaryls by C-H activation
Visible-Light-Triggered, Metal- and Photocatalyst-Free Acylation of N-Heterocycles
Atropodiastereoselective C-H Olefination of Biphenyl p-Tolyl Sulfoxides with Acrylates
Atroposelective synthesis of axially chiral P,S-ligands based on arynes
Construction of the biaryl-part of vancomycin aglycon via atropo-diastereoselective Suzuki-Miyaura coupling
Through-Space J(P,P) and J(P,F) Spin-Spin Coupling in C-1-Symmetric Biaryl Diphosphanes
Regioselectivity in the Aryne Cross-Coupling of Aryllithiums with Functionalized 1,2-Dibromobenzenes
Catalytic Palladium Phosphination: Modular Synthesis of C-1-Symmetric Biaryl-Based Diphosphines
Two Stereoinduction Events in One C−H Activation Step: A Route towards Terphenyl Ligands with Two Atropisomeric Axes
Iron-Catalyzed Minisci Type Acetylation of N-Heteroarenes Mediated by CH(OEt)3/TBHP
Stereoselective Sulfinyl Aniline-Promoted Pd-Catalyzed C−H Arylation and Acetoxylation of Aliphatic Amides
Asymmetric, Nearly Barrierless C(sp3)–H Activation Promoted by Easily-Accessible N-Protected Aminosulfoxides as New Chiral Ligands
Stereospecific C-H activation as a key step for the asymmetric synthesis of various biologically active cyclopropanes

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