Heterocyclic alkenes represent an important class of reactive feedstock and valuable
synthons for the synthesis of biologically important heterocyclic scaffolds. Although …

Conjugated dienes have occupied a pivotal position in the field of synthetic organic
chemistry and medicinal chemistry. They act as important synthons for the synthesis of …

The palladium-catalyzed oxidative C–H olefinations of uridine, deoxyuridine, uridine
monophosphate and uridine analogues are reported herein. This protocol provides an …

An efficient, microwave-assisted, oxidant-interceded, transition-metal-free, cross-
dehydrogenative C sp 2-C sp 3 coupling of C 8-Caffeine 2/Theobromine 3/theophylline 4 …

The pyridone fragment in the ligand [2, 2'‐bipyridin]‐6 (1H)‐one (bipy‐6‐OH) enables the
oxidative Heck reaction of simple arenes with oxygen as the sole oxidant and no redox …

The synthesis of pharmaceutically relevant scaffolds, such as substituted indoles or uracils,
through the alkenylation of the “enamine‐like” aromatic C− H bond is performed at room …

Over the past years, Pd (II)-catalyzed oxidative couplings have enabled the construction of
molecular scaffolds with high structural diversity via C–C, C–N and C–O bond-forming …

Developing an efficient catalytic system using molecular oxygen as the oxidant for rhodium-
catalyzed cross-dehydrogenative coupling remains highly desirable. Herein, rhodium …

We describe an efficient and versatile method for the direct C− H arylation of xanthines with
aryl halides using Pd/P (o‐tolyl) 3 as catalyst and Ag2O as an additive. Silver salts have …

The palladium‐catalyzed direct C–H olefination of unprotected uridine, 2′‐deoxyuridine,
uridine monophosphate, and uridine analogues are described here. This protocol provides …