Late-stage functionalization (LSF) introduces functional group or structural modification at
the final stage of the synthesis of natural products, drugs, and complex compounds. It is …

Transition metal‐catalyzed hydrofunctionalization of methylenecyclopropanes (MCPs) has
presented a considerable challenge due to the difficult manipulation of regioselectivity and …

The activation of C–C bonds via transition metal catalysis has become an increasingly
popular strategy in organic synthesis. An emerging method to cleave C–C bonds is to …

Rh (III)-catalyzed dienylation and cyclopropylation of 1, 2, 3-benzotriazinones with
alkylidenecyclopropanes (ACPs) has been achieved. Different from the previous reports of …

Considering the prevalence of spirocyclopropane motifs in bioactive compounds, the
development of efficient methods for the synthesis of various chiral spirocyclopropane motifs …

An efficient and new route for the synthesis of (E)-4-benzylideneisochroman-1-ones through
tandem cascade annulation of benzoic acids with alkylidenecyclopropanes using Ru (II) as …

An efficient method for the construction of various 3, 4, 5-trisubstituted phenol derivatives
has been achieved via the Rh (III)-catalyzed coupling of phosphonium cations with internal …

Herein, we report a Rh (III)-catalyzed C–H functionalization of indoles at the C4 position with
alkylidenecyclopropanes (ACPs). Motifs of dienes or cyclopropanes could be selectively …

The synthesis of dihydrobenzofuran scaffolds bears pivotal significance in the field of
medicinal chemistry and organic synthesis. These heterocyclic scaffolds hold immense …

A three component construction of conjugated 1, 3‐dienes bearing oxindoles or
isoquinolinediones from alkenylated aryl iodides, allenes and diazo compounds via a …