Conspectus The oxindole scaffold is a privileged structural motif that is found in a variety of
bioactive targets and natural products. Moreover, derivatives of the oxindole structure are …

Carbon dioxide (CO 2) is the main greenhouse gas and also an ideal C1 feedstock in
organic synthesis because it is abundant, non-toxic, nonflammable, and renewable. The …

Reductive carboxylation of organo (pseudo) halides with CO2 is a powerful method to
provide carboxylic acids quickly. Notably, the catalytic reductive carbo‐carboxylation of …

Bidentate P, N ligands, integrating phosphine and nitrogen donors, are highlighted for their
versatile characteristics, offering both electronic and steric tunability. Their hemilabile nature …

Herein, we report a nickel-catalyzed reductive cross-coupling reaction of easily accessible 3-
butenyl carbamoyl chloride with primary alkyl iodide to access the chiral α-alkylated …

Indoles are amongst the most essential class of heteroaromatics in organic chemistry, being
commonly found in biologically active natural products. Indole and its derivatives have …

Natural goods, medications, and pharmaceutically active substances all contain substituted
oxindoles. Generally, the C-3 stereocenter of the substituents of oxindoles and their absolute …

A mild visible-light-induced Pd-catalyzed one-pot three-component alkyl-carbamoylation
and cyanation of alkenes was developed. This general transformation, which proceeds via …

Amide bonds connect the amino acids in proteins and exist as a prevalent structural motif in
biomolecules. Herein, we have exploited the concept of cross‐electrophile coupling by …

Carbamoyl Fluoride-Enabled Enantioselective Ni-Catalyzed Carbocarbamoylation of
Unactivated Alkenes | Journal of the American Chemical Society ACS ACS Publications …