Indolizine (pyrrolo [1, 2-a] pyridine) is one of the five isomers of indole and it serves as a
precursor for widespread indolizidine alkaloids. The straightforward synthesis of indolizines …

Indolizine is a nitrogen-containing heterocycle that has a variety of potential biological
activities, and some indolizine derivatives with excellent fluorescence properties can even …

Visible-light-driven organic photochemical reactions have attracted substantial attention
from the synthetic community. Typically, catalytic quantities of photosensitizers, such as …

Vinyl boronates react with electron-deficient alkyl iodides in the presence of visible light to
give boronic esters in which two new C–C bonds have been created. The reaction occurs by …

In the last decade, visible light photoredox catalysis promoting radical‐based organic
transformations has received enormous synthetic applicability, as they allow unfolding of site …

A visible light‐induced (blue LED) radical cascade has been devised to effect selenylative
spirocyclization of N‐aryl alkynamides at room temperature under oxygen atmosphere and …

A photoinduced acylation of N‐heterocycles is explored. This visible‐light triggered reaction
occurs not only under extremely mild reaction conditions, but also does not require the …

Summary of main observation and conclusion We herein uncovered an electrochemical C—
H halogenation protocol that synergistically combines anodic oxidation and cathodic …

Oxosulfonylation is a difunctionalization protocol where oxo and sulfonyl groups are
introduced in one step to construct ketosulfones and N‐acylsulfonamides from simple and …

N-Iodosuccinimide catalyzed, visible-light-induced oxidative decarboxylative cross-coupling
between cinnamic acids and NH-sulfoximines is presented. This strategy results in the …