Ring-opening transformations of donor–acceptor cyclopropanes (DAC) with carbon-
centered nucleophiles is a simple, straight-forward approach to 1, 3-bifunctional compounds …

Nitrogen‐containing molecules are the key structural constituent of many pharmaceutical
compounds that play a pivotal role in drug development. Owing to their multifaceted …

Nitrogen-containing π-excessive aromatic heterocycles, in particular, carbazoles,
indolocarbazoles, benzocarbazoles, and carbolines have been considered the fundamental …

Carbazoles are privileged nitrogen heterocycles that are present in a wide range of natural
products, pharmaceuticals, and functional materials. Due to their wide application, various …

A highly enantioselective synthesis of chiral dihydro-3 H-carbazole-2-carboxylate
derivatives is reported via a “one-pot” cyclopentannulation-rearrangement cascade reaction …

Abstract A 1, 3‐aminothiolation was realized by reacting 2‐substituted cyclopropane 1, 1‐
dicarboxylates with sulfonamides and N‐(arylthio) succinimides. Under Sn (OTf) 2 catalysis …

Indolylmethanols have been recently involved in several processes dealing with indole
functionalization. These compounds, upon activation by Brønsted or Lewis acids, generate a …

We present a versatile method for the enantiospecific, cis-diastereoselective intermolecular
and intramolecular cycloaddition of donor–acceptor cyclopropanes to electron-poor alkenes …

A one-pot protocol for the synthesis of a tricyclic pseudoindoxyl scaffold from 2-
nitroalkynylbenzenes, comprising of an Au (III)-catalyzed nitroalkyne cycloisomerization …

The tetrahydrocarbazole (THC) motif is ubiquitous in natural products and biologically active
compounds. THCs can serve as favorable synthetic intermediates or precursors en-route to …