A number of methods have been adopted for the synthesis of amides; among these
methods, the oxidation of an amine to an amide is growing in interest as a means to prepare …

The Schmidt reaction has been an efficient and widely used synthetic approach to amides
and nitriles since its discovery in 1923. However, its application often entails the use of …

A visible-light-driven photoredox-catalyzed nonaqueous oxidative C–N cleavage of N, N-
dibenzylanilines to 2° amides is reported. Further, we have applied this protocol on 2 …

A visible‐light‐induced oxidation of diazenyl‐protected tetrahydroisoquinolines and
isoindolines for the synthesis of structurally diverse lactams is developed. The reaction was …

Abstract The 3, 4‐dihydroisoquinolin‐1 (2H)‐one motifs found in many natural products,
synthetic molecules with a diverse range of the biological activities and represent a privilege …

N-Alkyl and N-aryl-isoindolinones were prepared by a dioxane-mediated oxidation of
isoindoline precursors. The transformation exhibits unique chemoselectivity for …

Tetrabutylammonium hydroxide (TBAOH) was discovered as a highly efficient and green
catalyst for aerobic oxidation of the α-methylene carbon of primary amines as well as …

A novel C–H functionalization enabled multicomponent reaction involving N-heterocycles,
dinucleophile, and dipolarophile has been developed. Direct α-and more challenging β-C …

Using benzaldehydes, NaN (SiMe3) 2, and N-acylpyrroles, an operationally simple tandem
method to produce a wide array of 3, 4-dihydroisoquinolones is presented (37 examples …

In this paper, a selective synthesis of pyrrolidin-2-ones and 3-iodopyrroles via the cascade
reactions of N-substituted piperidines is presented. Mechanistically, the formation of …