Transition Metal-Catalyzed Direct Arylation of Substrates with Activated sp3-Hybridized C−H Bonds and Some of Their Synthetic Equivalents with Aryl Halides and …

F Bellina, R Rossi - Chemical reviews, 2010 - ACS Publications
Transition metal-catalyzed cross-coupling reactions of alkyl metals and aryl halides or
pseudohalides have emerged as a powerful methodology for the formation of Csp3-Csp2 …

Electroactive materials for organic electronics: preparation strategies, structural aspects and characterization techniques

A Pron, P Gawrys, M Zagorska, D Djurado… - Chemical Society …, 2010 - pubs.rsc.org
This critical review discusses specific chemical and physicochemical requirements which
must be met for organic compounds to be considered as promising materials for applications …

Transmetalation of unsaturated carbon nucleophiles from boron-containing species to the mid to late d-block metals of relevance to catalytic C− X coupling reactions …

DV Partyka - Chemical Reviews, 2011 - ACS Publications
Though often perceived as the simple metaphorical hybrid of synthetic inorganic and
organic chemistry, synthetic organometallic chemistry continues to vigorously differentiate …

Use of chiral sulfoxides in asymmetric synthesis

H Pellissier - Tetrahedron, 2006 - Elsevier
Although the first chiral organosulfur compounds were obtained at the beginning of this
century, they have received more attention since the early 1960s. Initially, chiral sulfur …

Highly diastereoselective Csp3–Csp2 Negishi cross-coupling with 1,2-, 1,3- and 1,4-substituted cycloalkylzinc compounds

T Thaler, B Haag, A Gavryushin, K Schober… - Nature Chemistry, 2010 - nature.com
Stereoselective functionalizations of organic molecules are of great importance to modern
synthesis. A stereoselective preparation of pharmaceutically active molecules is often …

Ni-catalyzed mild arylation of α-halocarbonyl compounds with arylboronic acids

C Liu, C He, W Shi, M Chen, A Lei - Organic letters, 2007 - ACS Publications
A simple yet powerful Ni catalyst can be used to promote direct arylations of α-halocarbonyl
compounds, including a range of esters, amides, and ketones, with various arylboronic acids …

Competitive and Selective Csp3Br versus Csp2Br Bond Activation in Palladium‐Catalysed Suzuki Cross‐Coupling: An Experimental and Theoretical Study of the …

C Mollar, M Besora, F Maseras… - … A European Journal, 2010 - Wiley Online Library
Phosphine ligands have been demonstrated to have an effect on reactivity and selectivity in
the competitive intramolecular palladium‐catalysed Suzuki–Miyaura coupling of dibromo …

Insertion of Isocyanides, Isothiocyanates, and Carbon Monoxide into the Pd− C Bond of Cyclopalladated Complexes Containing Primary Arylalkylamines of Biological …

J Vicente, I Saura-Llamas, JA García-López… - …, 2009 - ACS Publications
Cyclometalation of 3-(2-naphthyl)-d-alanine methyl ester is achieved by reacting the
corresponding hydrochloride salt and Pd (OAc) 2 in a 1: 1 molar ratio (acetonitrile, room …

Nickel-Catalyzed Reductive Arylation of α-Bromo Sulfoxide

Q Liu, T Lin, Y Wang, W Liang, L Cao, X Sheng… - Organic …, 2023 - ACS Publications
A nickel-catalyzed cross-electrophile coupling of aryl iodides with α-bromo sulfoxide to
access a diverse array of aryl benzyl sulfoxides has been discovered. These reactions …

Palladium‐Catalyzed Suzuki–Miyaura Reaction Involving a Secondary sp3 Carbon: Studies of Stereochemistry and Scope of the Reaction

N Rodríguez, C Ramirez de Arellano… - … A European Journal, 2007 - Wiley Online Library
Abstract Palladium‐catalyzed C C bond formation involving secondary sp3‐hybridized
carbon is described. These reactions occur with secondary 1‐bromoethyl arylsulfoxides and …