Unique examples of aza-Heck-based C(sp3)-H functionalization cascades are described. Under Pd(0)-catalyzed conditions, the aza-Heck-type cyclization of N-(pentafluorobenzoyloxy)carbamates generates alkyl-Pd(II) intermediates that effect C(sp3)-H palladation en route to cyclopropanes. Key factors that control the site selectivity of the cyclopropanation process have been elucidated such that selective access to a wide range of ring- or spiro-fused systems can be achieved
An intramolecular Cannizzaro-type hydride transfer to an in situ prepared allene enables the synthes...
We herein report a phosphine-catalyzed (3 + 2) annulation of cyclopropenones with a wide variety of ...
I. Lewis Acid-Promoted Carbon-Carbon Bond Cleavage of Aziridines: Divergent Cycloaddition Pathways o...
Ligand‐enabled aza‐Heck cyclizations and cascades of N‐(pentafluorobenzoyloxy)carbamates are describ...
Aza-Heck cyclizations initiated by oxidative addition of Pd0-catalysts into the N−O bond of N-(penta...
Amino alcohols, cyclopropanes and nitriles are privileged structural motifs found in the scaffold of...
The functionalization of aliphatic C (sp3)-H bonds using Pd catalysis has emerged as a powerful, ste...
In the past years, Pd0-catalyzed C(sp3)-H activation provided efficient and step-economical methods ...
The author thanks EaStCHEM for financial support.Recently Antonchick and Manna described a unique an...
In this contribution, we report novel palladium-catalyzed carbonylative cascade approaches to highly...
There is a continuous need for designing new and improved synthetic methods aiming at minimizing rea...
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ...
1,n-Metal shift is an elegant alternative approach enabling the functionalization of remote C H bond...
Cyclopropanes are encountered in several natural and synthetic products displaying a wide range of b...
The combination of palladium catalysis and thermal cycloaddition is shown to transform tricyclic azi...
An intramolecular Cannizzaro-type hydride transfer to an in situ prepared allene enables the synthes...
We herein report a phosphine-catalyzed (3 + 2) annulation of cyclopropenones with a wide variety of ...
I. Lewis Acid-Promoted Carbon-Carbon Bond Cleavage of Aziridines: Divergent Cycloaddition Pathways o...
Ligand‐enabled aza‐Heck cyclizations and cascades of N‐(pentafluorobenzoyloxy)carbamates are describ...
Aza-Heck cyclizations initiated by oxidative addition of Pd0-catalysts into the N−O bond of N-(penta...
Amino alcohols, cyclopropanes and nitriles are privileged structural motifs found in the scaffold of...
The functionalization of aliphatic C (sp3)-H bonds using Pd catalysis has emerged as a powerful, ste...
In the past years, Pd0-catalyzed C(sp3)-H activation provided efficient and step-economical methods ...
The author thanks EaStCHEM for financial support.Recently Antonchick and Manna described a unique an...
In this contribution, we report novel palladium-catalyzed carbonylative cascade approaches to highly...
There is a continuous need for designing new and improved synthetic methods aiming at minimizing rea...
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ...
1,n-Metal shift is an elegant alternative approach enabling the functionalization of remote C H bond...
Cyclopropanes are encountered in several natural and synthetic products displaying a wide range of b...
The combination of palladium catalysis and thermal cycloaddition is shown to transform tricyclic azi...
An intramolecular Cannizzaro-type hydride transfer to an in situ prepared allene enables the synthes...
We herein report a phosphine-catalyzed (3 + 2) annulation of cyclopropenones with a wide variety of ...
I. Lewis Acid-Promoted Carbon-Carbon Bond Cleavage of Aziridines: Divergent Cycloaddition Pathways o...