Results 231 to 240 of about 2,273,903 (330)
Abstract Photochemical C−C coupling reactions can be tailored to industrial chemical processes and preparations of pharmaceuticals. Recent approaches in this area are limited to using precious transition metal coordination complexes that facilitate light absorption and redox processes with benchtop chemicals. Herein, we propose a paradigm that involves
Samjhana Maharjan+9 more
wiley +1 more source
Isolation, structural elucidation, and integrated biological and computational evaluation of antidiabetic labdane diterpenes from <i>Curcuma zedoaria</i> rhizomes. [PDF]
Le TH+8 more
europepmc +1 more source
Abstract While arylazo sulfones have been widely applied as arylating agents, their exploitation for diazenylation reactions has been previously limited to electron‐rich alkenes such as styrenes and silyl enol ethers. Herein we optimized a synthetic one‐pot protocol to access oxazolyl azo compounds via a selective domino ring‐closing/aryldiazenylation ...
Enzo Delalande+5 more
wiley +1 more source
Triptycepenes: Synthesis, Metal Complexes, and Their Reactivity in Catalytic Reactions. [PDF]
Mothuku SS, Monkowius U, Hapke M.
europepmc +1 more source
Abstract Additive carbonylations typically necessitate strong nucleophiles, such as alcohols or amines. In this study, we carbonylated a poorly nucleophilic urea, under oxidant‐free conditions. Our straightforward carbonylative strategy enables access to versatile α,β‐unsaturated γ‐lactams featuring an aminocarbonyl fragment, utilizing readily ...
Debora Schiroli+11 more
wiley +1 more source
Stereoselective Synthesis of Nucleotide Analog Prodrugs (ProTides) via an Oxazaphospholidine Method. [PDF]
Nakamura M, Kakuta K, Sato K, Wada T.
europepmc +1 more source
Improving the Photochemical Skeletal Enlargement of Pyridines to 1,2‐Diazepines with Isocyanates
Abstract In this work, we extend the one‐pot protocol to synthesize 1,2‐diazepines from commercially available and cheap starting materials. Capitalizing on isocyanate derivatives as activating agents, the photochemical skeletal enlargement occurs, while preserving key functional groups embedded in more than 30 substrates.
Clément Ghiazza+3 more
wiley +1 more source
Abstract Mg(SPh)2 has been found to be a highly active catalyst in photocatalytic alkylation reactions of active methylene compounds with nonactivated alkenes. The desired reactions proceeded smoothly to afford the corresponding alkylated products in high yields with low catalyst loadings (0.2–0.3 mol%). This protocol is applicable to a continuous‐flow
Yasuhiro Yamashita+3 more
wiley +1 more source
In the presence of a Pd0 catalyst, large π‐extended arynes trimerize in an unusual manner to forge extremely compact and strained chiral benzenoids. This new trimerization reaction involves a 1,7‐Pd isomerization, a rare and poorly understood process that is elucidated.
Albert Artigas+6 more
wiley +1 more source