The development of new green methodologies and their broader adoption for promoting
sustainable development in chemistry laboratories and industry play a significant role in …

In recent years, para-quinone methides (p-QMs) have emerged as attractive and versatile
synthons in organic synthesis owing to their high reactivity. Consequently, p-QM chemistry …

An atom-and step-economical, efficient and eco-friendly method for constructing
naphthoselenazol-2-amines through a visible-light photocatalytic multi-component reaction …

In the past decade, multicomponent reactions have experienced a renaissance as powerful
peptide macrocyclization tools enabling the rapid creation of skeletal complexity and …

The Petasis boron–Mannich reaction, simply referred to as the Petasis reaction, is a
powerful multicomponent coupling reaction of a boronic acid, an amine, and a carbonyl …

Herein, the l-serine-functionalized metal–organic framework nanostructure is obtained via a
simple two-step post-synthetic modification strategy. Interesting properties of serine, such as …

Historically, the use of mechanochemical methods in synthesis has been almost negligible,
but their perception by the synthetic community has changed in recent years and they are on …

With the growing interest in renewable energy and global warming, it is important to
minimize the usage of hazardous chemicals in both academic and industrial research …

Organic transformations that involve direct functionalization of C–H bonds represent an
attractive synthetic strategy that maximizes atom-and step-economy. With the generally high …

Biginelli reaction involves acid-catalyzed one-pot synthesis of 3, 4-dihydropyrimidin-2 (1 H)-
ones (DHPMs) using easily-accessible starting materials, namely, aldehyde, active …