CO 2 is an important C1 resource. We report a method for the synthesis of pharmacologically active 2oxazolidinones by reacting CO 2 with allylic amines. As opposed to previous addition reactions, the unsaturated double bonds are preserved. Thus, the product is more plastic and easier to use for subsequent structural modification. Furthermore, this method can also be applied to the synthesis of six-membered heterocycles (1,3oxazinan-2-ones) and the participation of a low concentration of CO 2 , indicating it has certain practicability.

A palladium‐catalyzed tandem cyclization of 2‐(2‐ethynylphenyl)acetonitriles with isocyanides has been developed. Various indeno[2,1‐b]pyrroles were prepared in 55%–82% yields under air atmosphere at 100 °C. The key to the success of this protocol is construction of new C−C and C−N bonds via the orderly insertion of isocyanides.

Methanol plays a crucial role in organic synthesis as a green C1 source. Herein, the concise α-methoxymeth- ylation and aminomethylation of propiophenones is achieved via electrochemistry with methanol as both...

A Pd-catalyzed cyclization reaction of 2-(2vinylarene)acetonitriles and isocyanides has been documented. Various naphthalen-2-amines were obtained in moderate to good yields under mild conditions. The in vitro cytotoxicity of all products was evaluated by MTT assay against seven human cancer cell lines. The results indicated that compounds 3ea, 3ma, and 3ob exhibited effective anticancer activities against the tested cancer cells.

The novel method for the synthesis of gem-bisarylthio enamines and α-phenylthio ketones was developed via the coupling of α-substituted vinyl azides with thiols in the presence of tetrabutylammonium iodide (TBAI) as a redox catalyst and electrolyte at room temperature. Electronic properties were crucial in the generated products. This protocol features metal- and oxidant-free materials, broad tolerance of substrates, and mild reaction conditions.