Carbon monoxide is an indispensable C1 building block that has been recognized as a
potent feedstock for synthesizing carbonyl-containing molecules. Carbonylative reactions …

The pyrrolo [1, 2-a] indole unit is a privileged heterocycle found in numerous natural
products and has been shown to exhibit diverse pharmacological properties. Thus, recent …

Carbonylation, an efficient and straightforward approach for installing a carbonyl group into
their parent compounds, is an important area in modern organic synthesis. This Review …

The Rh (III)-catalyzed C–H oxidative alkylation of aniline derivatives with readily available
secondary allyl alcohols using a pyrimidine-directing group, leading to the production of β …

Isoindolinone structure is an important privileged scaffold found in a large variety of naturally
occurring as well as synthetic, biologically and pharmaceutically active compounds. Owing …

Rhodium-catalyzed substrate-tunable oxidative annulation and spiroannulation reactions of
2-arylindoles with benzoquinone leading to 9 H-dibenzo [a, c] carbazol-3-ols and new …

An efficient and regioselective synthesis of fused polycyclic furo [3, 4-c] indolo [2, 1-a]
isoquinolines through Rh (III)-catalyzed cascade C–H activation/annulation/lactonization of …

A protocol for palladium-catalyzed C–H carbonylation of readily available free primary
benzylamines using NH2 as the chelating group under an atmospheric pressure of CO has …

Readily available N-carbamoyl indolines can be converted into highly valuable 2-alkenyl
and 2-alkyl indoles in a one-pot reaction, through an autotandem catalytic cascade …

This work reports the experimentally studied mechanochemical formation of rhodacycles by
ball milling pyridine‐and quinoline‐derived substrates and [Cp* RhCl2] 2 in the presence of …