C–H functionalization has been emerging as a powerful method to establish carbon–carbon
and carbon–heteroatom bonds. Many efforts have been devoted to transition-metal …

Readily accessible and shelf-stable 1, 2, 3-triazole and its analogues such as pyridotriazole,
triazoloindole, benzotriazole, and thiadiazole exist in equilibrium with their ring-opened …

In the past decades, an enormous number of reports have been dedicated towards the
synthesis of nitrogen containing heterocycles. This immense interest have emerged owing to …

Efficient control of regioselectivity is a key concern in transition-metal-catalyzed direct C–H
functionalization reactions. Various strategies for regiocontrol have been established by …

Over the past decade, α‐imino carbenoids generated via transition metal (such as rhodium,
nickel, copper, palladium, silver) catalyzed denitrogenative ring‐opening of N‐sulfonyl‐1, 2 …

Abstract β‐Carboline and its derivatives are well‐known for their biological and
pharmacological properties and are considered as an important source of drug or drug …

A method for the synthesis of densely substituted 4-pyrrolin-2-ones by Rh (II)-catalyzed
denitrogenative transannulation of 1-alkyl-4-aryl-1 H-1, 2, 3-triazoles with diazo esters has …

Short and efficient synthesis of heterocyclic compounds are highly desirable in synthetic
organic chemistry. It is a dream approach to accomplish these syntheses from readily …

Five membered N‐heterocycles are significant targets in organic synthesis because of their
ubiquitous existence in bioactive natural products and pharmaceuticals. Over the past …

An efficient palladium-catalyzed approach to access various functionalized (Z)-3-
benzylidene-isoindoline-1-ones and (Z)-3-benzylidene (imino) isobenzofuranones via a …