In this review, we want to explain how the burning of fossil fuels is pushing us towards green
energy. Actually, for a long time, we have believed that everything is profitable, that …

In the present work, a convenient and straightforward approach to the preparation of
borylated amidines based on the closo-dodecaborate anion [B12H11NCCH3NHR]−, R= H …

A recent study showed that a Mn-pincer could catalyze the acceptorless dehydrogenative
coupling of nitriles and alcohols to yield acrylonitriles. The reaction mechanism proposed in …

The synthesis of methyl 5-aminopyrrole-3-carboxylates from 4-methyleneisoxazol-5-ones
via “cyanide Michael addition/methylation/reductive isoxazole-pyrrole transformation” is …

Recent advances in the environmentally benign synthesis of common heterocycles are
described. This account features three main parts; the preparation of non-aromatic …

A straightforward method for ring opening of donor–acceptor cyclopropanes with
trimethylsilyl cyanide as a surrogate of cyanide ion in the presence of B (C6F5) 3 or …

An efficient and environmentally friendly synthetic approach toward functionalized
dihydropyrrole derivatives is reported. The developed protocol proceeds via chemoselective …

We herein describe a simple and metal-free domino methodology to synthesize 2-
aminopyrroles from alkynyl vinyl hydrazides. The domino reaction involves a novel …

Herein, we report a Pd (0)-catalyzed cascade reaction of intramolecular indolyl isocyanide-
insertion, isocyanide-initiated scaffold-rearrangement with indolyl migration and redox …

An efficient, tandem one-pot approach to synthesize multisubstituted 2-acylpyrroles from
readily prepared N-tosyl triazoles and 2-hydroxymethylallyl carbonates is reported. The …