Catalytic transformation of ubiquitous C–H bonds into valuable C–N bonds offers an efficient
synthetic approach to construct N-functionalized molecules. Over the last few decades …

Sulfoximines are widely used as medicines, agricultural chemicals, chiral precursors, and
chiral ligands in asymmetric synthesis, as well as pivotal intermediates for the construction of …

Within the last few years, oxidative activation reactions of CÀ H/NÀH or CH/OÀH bond
combinations with subsequent alkyne or alkene annulations have become the synthetically …

Sulfoximine and its congeners are a versatile class of structural motifs widely found in a
plethora of pharmaceutical compounds and crop protection industries due to their …

Development of C–N coupling processes is fundamentally important and challenging for the
synthesis of biologically active molecules and drugs. Herein, we report a highly atom …

A microwave-assisted, Cp* CoIII-catalyzed direct C–H activation/double C–N bond formation
reaction of simple N H-sulfoximines with 1, 4, 2-dioxazol-5-ones to produce diverse …

The omnipresence of Csingle bondH bonds in organic compounds renders them highly
attractive targets for the installation of functional groups towards the construction of valuable …

During the last one and half decades, chemists within vastly different areas of science have
witnessed a rising interest in chemical matters incorporating the sulfonimidamide functional …

Enamines and enamides are useful synthetic intermediates and common components of
bioactive compounds. A new protocol for their direct synthesis by a net alkene C H …

A Ru (II)‐catalyzed approach for the rapid assembly of 1, 2‐benzothiazines has been
developed to enable the coupling‐cyclization of aryl Csp2− H bonds with α‐carbonyl …