1,n-Metal shift is an elegant alternative approach enabling the functionalization of remote C H bonds from simple precursors. In this work, we report a novel and simple Pd-0-catalyzed domino reaction involving 1,4-palladium shift and C(sp(3))-H activation and leading to (fused) five-membered rings. This method allowed access to a broad range of valuable arylidene gamma-lactams and indanones and was applied to the formal synthesis of (-)-pyrrolam
Despite the emergence of catalytic C(sp3 )−H arylation at the remote δ-position via challenging six-...
The selective activation of C–C bonds holds vast promise for catalysis. So far, research has been p...
Metal-catalyzed cross-coupling reactions to form C-C bonds are a mainstay in the preparation of smal...
1,n-Metal shift is an elegant alternative approach enabling the functionalization of remote C–H bond...
In the past years, Pd0-catalyzed C(sp3)-H activation provided efficient and step-economical methods ...
Over the past decades, the transition metal-catalysed intramolecular activation of unactivated C-H b...
The functionalization of aliphatic C (sp3)-H bonds using Pd catalysis has emerged as a powerful, ste...
La fonctionnalisation de liaisons C-H réputées peu réactives ouvre de nouvelles perspectives en synt...
A variety of strained α-alkylidene-γ-lactams were synthesized by palladium(0)-catalyzed intramolecul...
CONSPECTUS: The catalytic activation and functionalization of unactivated C(sp(3))-H bonds of alkyl ...
La fonctionnalisation directe des liaisons C-H représente une avancée considérable dans la re...
Palladium catalysed β-C(sp3)–H activation of tertiary aldehydes using a transient imine directing gr...
Despite the emergence of catalytic C(sp3 )−H arylation at the remote δ-position via challenging six-...
The search for new and distinct disconnection strategies is one of the foremost challenges in synthe...
A new method for the preparation of 2,2-disubstituted indolines from 2-phenylethylamines was develop...
Despite the emergence of catalytic C(sp3 )−H arylation at the remote δ-position via challenging six-...
The selective activation of C–C bonds holds vast promise for catalysis. So far, research has been p...
Metal-catalyzed cross-coupling reactions to form C-C bonds are a mainstay in the preparation of smal...
1,n-Metal shift is an elegant alternative approach enabling the functionalization of remote C–H bond...
In the past years, Pd0-catalyzed C(sp3)-H activation provided efficient and step-economical methods ...
Over the past decades, the transition metal-catalysed intramolecular activation of unactivated C-H b...
The functionalization of aliphatic C (sp3)-H bonds using Pd catalysis has emerged as a powerful, ste...
La fonctionnalisation de liaisons C-H réputées peu réactives ouvre de nouvelles perspectives en synt...
A variety of strained α-alkylidene-γ-lactams were synthesized by palladium(0)-catalyzed intramolecul...
CONSPECTUS: The catalytic activation and functionalization of unactivated C(sp(3))-H bonds of alkyl ...
La fonctionnalisation directe des liaisons C-H représente une avancée considérable dans la re...
Palladium catalysed β-C(sp3)–H activation of tertiary aldehydes using a transient imine directing gr...
Despite the emergence of catalytic C(sp3 )−H arylation at the remote δ-position via challenging six-...
The search for new and distinct disconnection strategies is one of the foremost challenges in synthe...
A new method for the preparation of 2,2-disubstituted indolines from 2-phenylethylamines was develop...
Despite the emergence of catalytic C(sp3 )−H arylation at the remote δ-position via challenging six-...
The selective activation of C–C bonds holds vast promise for catalysis. So far, research has been p...
Metal-catalyzed cross-coupling reactions to form C-C bonds are a mainstay in the preparation of smal...