Transition-metal-catalyzed C–S, C–Se, and C–Te bond formations via cross-coupling and atom-economic addition reactions. Achievements and challenges

IP Beletskaya, VP Ananikov - Chemical Reviews, 2022 - ACS Publications
In the present review, we discuss recent progress in the field of C–Z bond formation
reactions (Z= S, Se, Te) catalyzed by transition metals. Two complementary methodologies …

Synthesis of sulfones via selective C–H-functionalization

S Shaaban, S Liang, NW Liu… - Organic & Biomolecular …, 2017 - pubs.rsc.org
The synthesis of sulfones via a selective functionalization of C–H-bonds represents a
powerful alternative to classical methods for the preparation of this important compound …

The Suzuki–Miyaura coupling of nitroarenes

MR Yadav, M Nagaoka, M Kashihara… - Journal of the …, 2017 - ACS Publications
Synthesis of biaryls via the Suzuki–Miyaura coupling (SMC) reaction using nitroarenes as
an electrophilic coupling partners is described. Mechanistic studies have revealed that the …

Transition-metal-catalyzed denitrative coupling of nitroarenes

K Muto, T Okita, J Yamaguchi - ACS Catalysis, 2020 - ACS Publications
Functionalization of arenes is a topic of central importance in diverse fields ranging from
medicinal chemistry to materials science. Metal-catalyzed cross-coupling and nucleophilic …

Recent Methodologies That Exploit Oxidative Addition of C–N Bonds to Transition Metals

J Garcı́a-Cárceles, KA Bahou, JF Bower - ACS Catalysis, 2020 - ACS Publications
The activation of σ-bonds by transition metals underpins a wide range of methods for the
synthesis of complex molecules. Within this context, C–N bond activation has emerged …

Alkylative dearomatization by using an unactivated aryl nitro group as a leaving group: access to diversified alkylated spiro [5.5] trienones

D Xia, XF Duan - Organic Letters, 2021 - ACS Publications
The cleavage of an unactivated aryl nitro group triggered by alkyl radicals enables a
dearomative cyclization, affording diversified alkylated spiro [5.5] trienones in good yields …

Safe, Scalable, Inexpensive, and Mild Nickel‐Catalyzed Migita‐Like C− S Cross‐Couplings in Recyclable Water

TY Yu, H Pang, Y Cao, F Gallou… - Angewandte Chemie …, 2021 - Wiley Online Library
A new approach to C− S couplings is reported that relies on nickel catalysis under mild
conditions, enabled by micellar catalysis in recyclable water as the reaction medium. The …

Sterically hindered N-heterocyclic carbene/palladium (ii) catalyzed Suzuki–Miyaura coupling of nitrobenzenes

K Chen, W Chen, X Yi, W Chen, M Liu… - Chemical …, 2019 - pubs.rsc.org
Palladium-catalyzed denitrative Suzuki coupling of nitroarenes using 2-aryl-5-(2, 4, 6-
triisopropylphenyl)-2, 3-imidazolylidene [1, 5-a] pyridines as the ligands is described. The …

Convenient MW-assisted synthesis of unsymmetrical sulfides using sulfonyl hydrazides as aryl thiol surrogate

N Singh, R Singh, DS Raghuvanshi, KN Singh - Organic letters, 2013 - ACS Publications
Convenient MW-Assisted Synthesis of Unsymmetrical Sulfides Using Sulfonyl Hydrazides as
Aryl Thiol Surrogate | Organic Letters ACS ACS Publications C&EN CAS Find my institution Log …

Copper-catalyzed thioetherification reactions of alkyl halides, triphenyltin chloride, and arylboronic acids with nitroarenes in the presence of sulfur sources

A Rostami, A Rostami, A Ghaderi - The Journal of Organic …, 2015 - ACS Publications
In this article, we report three odorless methods for the thioarylation and thioalkylation of
different nitroarenes using alkyl halides (Br, Cl), triphenyltin chloride, and arylboronic acids …