Light-Triggered, Ni-Catalyzed Cyanation of Aryl Triflates with 1, 4-Dicyanobenzene as the CN Source
Y Yan, P Wang, Y Wang, J Dong, G Li, C Wang… - Organic …, 2024 - ACS Publications
A light-triggered, Ni-catalyzed cyanation of aryl triflates was herein reported, which provides
a benign photochemical synthesis of aryl nitriles using 1, 4-dicyanobenzene as the CN …
a benign photochemical synthesis of aryl nitriles using 1, 4-dicyanobenzene as the CN …
Visible-Light-Induced Regioselective Radical-Polar Crossover 1, 4-Hydrophosphinylation of 1, 3-Enynes: Access to Trisubstituted Allenes Bearing a Phosphine Oxide …
Q Cao, MM Li, X Mao, QQ Zhou, W Ding - Organic Letters, 2024 - ACS Publications
The radical 1, 4-functionalizations of 1, 3-enynes have emerged as a powerful strategy for
the synthesis of multisubstituted allenes. However, the phosphorus-centered radical-initiated …
the synthesis of multisubstituted allenes. However, the phosphorus-centered radical-initiated …
Nickel-catalyzed cyanation of CS bond using CO2 and NH3
Q Shi, Y Li, Y Li, Y Dong, Z Li, L He, L Sun, Y Li - Journal of Catalysis, 2024 - Elsevier
Catalytic cleavage of Csingle bondS bonds is an important approach in the construction of
functionalized molecules. Herein, we developed the catalytic synthesis of nitriles from …
functionalized molecules. Herein, we developed the catalytic synthesis of nitriles from …
Manganese Promoted Reductive Cross‐Coupling of Phosphine Chlorides with Disulfides for the Synthesis of Thiophosphanes
CP Zhang, TZ Wang, ZJ Yang… - Advanced Synthesis & …, 2024 - Wiley Online Library
Herein we reported a manganese promoted reductive cross‐coupling approach to construct
P‒S bond. This is a practical method for the synthesis of mono‐thiophosphanes, bis …
P‒S bond. This is a practical method for the synthesis of mono‐thiophosphanes, bis …
[HTML][HTML] Nickel-Catalyzed Reductive Cyanation of Aryl Halides and Epoxides with Cyanogen Bromide
YJ Wu, C Ma, M Bilal, YF Liang - Molecules, 2024 - mdpi.com
Nitriles are valuable compounds because they have widespread applications in organic
chemistry. This report details the nickel-catalyzed reductive cyanation of aryl halides and …
chemistry. This report details the nickel-catalyzed reductive cyanation of aryl halides and …
Chromium‐Catalyzed Reductive Cross‐Coupling to Construct C− SS Bonds from Unactivated Alkyl Electrophiles
CP Zhang, TZ Wang, K Wu, YF Liang - ChemCatChem, 2024 - Wiley Online Library
Low‐valent chromium catalysts are cheap and less toxic compared to other transition metal
catalysts. Here in, we reported a ligand‐free chromium (III)‐catalyzed manganese reductive …
catalysts. Here in, we reported a ligand‐free chromium (III)‐catalyzed manganese reductive …
Photoinduced radical-polar-crossover cyanomethylation-cyclization cascade of unactivated N-alkene-linked indoles with bromoacetonitrile towards cyanomethylated …
Q Wang, L Fu, Z Gao, J Huang, L Zhang, H Wang… - Molecular …, 2024 - Elsevier
Unactivated N-alkene-linked indoles were established as general substrates for
cyanomethylation-cyclization cascade reactions with bromoacetonitrile in a photoinduced …
cyanomethylation-cyclization cascade reactions with bromoacetonitrile in a photoinduced …
Using Metallaphotoredox Towards the Synthesis of Aryl Nitriles and α-Aryl Nitriles
MA Reed, ADM Jeanneret - Synfacts, 2024 - thieme-connect.com
Significance: Nitriles are often used as a key intermediate in many synthetic routes due to
their versatile nature. They can be transformed into a variety of useful functional groups and …
their versatile nature. They can be transformed into a variety of useful functional groups and …