Natural product-inspired compound collections serve as excellent sources for the
identification of new bioactive compounds to treat disease. However, such compounds must …

When “dark” is bright: the scarcely explored electrophilic profile of the indolyl core (dark‐
side) continues to inspire developments in organic synthesis by means of new catalytic …

Organonitrogen chemicals, such as amines, nitriles, amides, amino acids, and N-
heterocycles, are ubiquitous building blocks in chemical industry. Conventional …

Abstract 2, 4, 6‐Triphenylpyrylium (TPT+) functions as a classic organic photocatalyst and
exhibits a noteworthy absorption in the visible range, strongly oxidizing excited states, and a …

Indoles are one of the most prominent aromatic heterocycles in the organic chemistry field.
Due to their widespread presence in various natural products, alkaloids, drugs, approved …

A metal-free one-pot oxidative cross-dehydrogenation coupling reaction for the formation of
C–N/C–C bonds at the C2, 3-positions of indoles with azoles and quinoxalinones has been …

A Ni-catalyzed reaction was developed for the synthesis of multifunctionalized indoles. The
reaction proceeded through oxidative cyclization of the Ni (0)/P^ N complex with an enyne …

Indole is the most frequently found heterocyclic core structures in pharmaceuticals, natural
products, agrochemicals, dyes and fragrances. For about 150 years, chemists were …

Indole heterocycles hold an important position in chemical landscape because of their
prominence in natural products and pharmaceuticals. Consequently, development of new …

An efficient catalytic strategy toward the synthesis of N-substituted 3-methylindoles from
inactive o-dihaloarenes and N-allylamines was developed by using a 1, 3-bis (2, 6 …