Recent development of aryl diazonium chemistry for the derivatization of aromatic compounds

F Mo, D Qiu, L Zhang, J Wang - Chemical Reviews, 2021 - ACS Publications
Aryl diazonium salts are versatile building blocks in organic synthesis. In light of the ever-
increasing importance of aryl diazonium salts spanning most disciplines of the chemical …

Palladium-catalyzed cross-coupling reactions: a powerful tool for the synthesis of agrochemicals

P Devendar, RY Qu, WM Kang, B He… - Journal of agricultural …, 2018 - ACS Publications
Pd-catalyzed cross-coupling reactions have become essential tools for the construction of
carbon–carbon and carbon–heteroatom bonds. Over the last three decades, great efforts …

Activation of C–O and C–N bonds using non-precious-metal catalysis

TB Boit, AS Bulger, JE Dander, NK Garg - ACS catalysis, 2020 - ACS Publications
Metal-catalyzed cross-couplings represent one of the most important reaction platforms in
modern synthetic chemistry (Figure 1 A). 1 Although the field enjoys a rich history, there …

Recent Advances in Palladium‐Catalyzed Cross‐Coupling Reactions at ppm to ppb Molar Catalyst Loadings

D Roy, Y Uozumi - Advanced Synthesis & Catalysis, 2018 - Wiley Online Library
We review here new developments in decreasing the catalyst loadings in palladium‐
catalyzed C–C bond‐formation reactions to mol ppm or mol ppb levels. This decreases the …

Biaryl synthesis with arenediazonium salts: cross-coupling, CH-arylation and annulation reactions

FX Felpin, S Sengupta - Chemical Society Reviews, 2019 - pubs.rsc.org
The rich legacy of arenediazonium salts in the synthesis of unsymmetrical biaryls, built
around the seminal works of Pschorr, Gomberg and Bachmann more than a century ago …

A need for caution in the preparation and application of synthetically versatile aryl diazonium tetrafluoroborate salts

JD Firth, IJS Fairlamb - Organic Letters, 2020 - ACS Publications
Since their discovery 1 in 1858, aryl diazonium salts have played a major role in organic
synthesis. They have been widely employed as precursors to diazo dyes 2 and synthetic …

Visible-Light-mediated deaminative three-component dicarbofunctionalization of styrenes with benzylic radicals

FJR Klauck, H Yoon, MJ James, M Lautens… - ACS …, 2018 - ACS Publications
The visible-light-mediated three-component dicarbofunctionalization of styrenes using
simple benzylic radicals is described. Notably, this work describes a rare example of …

A Heck–Matsuda Process for the Synthesis of β‐Arylethenesulfonyl Fluorides: Selectively Addressable Bis‐electrophiles for SuFEx Click Chemistry

HL Qin, Q Zheng, GAL Bare, P Wu… - Angewandte Chemie …, 2016 - Wiley Online Library
A Heck–Matsuda process for the synthesis of the otherwise difficult to access compounds, β‐
arylethenesulfonyl fluorides, is described. Ethenesulfonyl fluoride (ie, vinylsulfonyl fluoride …

Recent advances in the synthesis of nitrogen heterocycles using arenediazonium salts as nitrogen sources

J Liu, J Jiang, L Zheng, ZQ Liu - Advanced Synthesis & …, 2020 - Wiley Online Library
Nitrogen heterocycles are important structural subunits that occur widely in bioactive natural
products, pharmaceuticals, agrochemicals, dyes, cosmetics, and functional materials …

Radical-mediated oxidative annulations of 1, n-enynes involving C–H functionalization

Y Li, GA Pan, MJ Luo, JH Li - Chemical Communications, 2020 - pubs.rsc.org
The 1, n-enyne annulation reaction has emerged as one of the most powerful and
straightforward tools to build carbo-and hetero-cyclic frameworks that are found in numerous …