Recent progress in cyclic aryliodonium chemistry: syntheses and applications

X Peng, A Rahim, W Peng, F Jiang, Z Gu… - Chemical …, 2023 - ACS Publications
Hypervalent aryliodoumiums are intensively investigated as arylating agents. They are
excellent surrogates to aryl halides, and moreover they exhibit better reactivity, which allows …

Cycloaddition reactions of enoldiazo compounds

QQ Cheng, Y Deng, M Lankelma… - Chemical Society Reviews, 2017 - pubs.rsc.org
Enoldiazo esters and amides have proven to be versatile reagents for cycloaddition
reactions that allow highly efficient construction of various carbocycles and heterocycles …

Asymmetric Three-Component Reaction of Enynal with Alcohol and Imine as An Expeditious Track to Afford Chiral α-Furyl-β-amino Carboxylate Derivatives

K Hong, J Shu, S Dong, Z Zhang, Y He, M Liu… - ACS …, 2022 - ACS Publications
Herein, we report an achiral dirhodium complex and chiral phosphoric acid cooperatively
catalyzed asymmetric three-component reaction of enynal with alcohol and imine, affording …

Visible-light-induced [1+ 5] annulation of phosphoryl diazomethylarenes and pyridinium 1, 4-zwitterionic thiolates

S Sun, Y Wei, J Xu - Organic Letters, 2022 - ACS Publications
Visible-light-induced [1+ 5] annulation of phosphoryl diazomethylarenes and pyridinium 1, 4-
zwitterionic thiolates generates various trifunctionalized dialkyl 1-phosphoryl-1, 9a …

Transition‐Metal‐Catalyzed C−H Bond Functionalization of Arenes/Heteroarenes via Tandem C−H Activation and Subsequent Carbene Migratory Insertion Strategy

N Jha, NP Khot, M Kapur - The Chemical Record, 2021 - Wiley Online Library
The past decade has witnessed tremendous developments in transition‐metal‐catalyzed C−
H bond activation and subsequent carbene migratory insertion reactions, thus assisting in …

Gold (I)-catalyzed intramolecular cyclization/intermolecular cycloaddition cascade as a fast track to polycarbocycles and mechanistic insights

C Zhang, K Hong, C Pei, S Zhou, W Hu… - Nature …, 2021 - nature.com
Metal carbene is an active synthetic intermediate, which has shown versatile applications in
synthetic chemistry. Although a variety of catalytic methods have been disclosed for the …

Enantioselective α-Boryl Carbene Transformations

MY Huang, JB Zhao, CD Zhang, YJ Zhou… - Journal of the …, 2024 - ACS Publications
Carbenes, recognized as potent intermediates, enable unique chemical transformations,
and organoborons are pivotal in diverse chemical applications. As a hybrid of carbene and …

Chemoselective hydro (chloro) pentafluorosulfanylation of diazo compounds with pentafluorosulfanyl chloride

JY Shou, XH Xu, FL Qing - Angewandte Chemie International …, 2021 - Wiley Online Library
Pentafluorosulfanyl chloride (SF5Cl) is the most prevalent reagent for the incorporation of
SF5 group into organic compounds. However, the preparation of SF5Cl often relies on …

Tunable vicinal, geminal diphosphorylation and C–N bond phosphorylation of enaminones toward divergent phosphorylated ketone derivatives

D Cao, C Wang, JP Wan, C Wen, Y Liu - Chemical Communications, 2023 - pubs.rsc.org
This paper reports the trifunctionalization reactions of tertiary enaminones in the fashion of
selective gem-and vicinal diphosphorylation, leading to the tunable synthesis of α, α-and α …

Copper-Catalyzed Cascade Cyclization Reactions of Diazo Compounds with tert-Butyl Nitrite and Alkynes: One-Pot Synthesis of Isoxazoles

XD Wang, LH Zhu, P Liu, XY Wang… - The Journal of …, 2019 - ACS Publications
A novel copper-catalyzed [3+ 2] cycloaddition reaction of alkynes with nitrile oxides
generated in situ from the coupling reaction of copper carbene and nitroso radical has been …