Transition-metal-catalyzed cross-coupling reactions have been well-established as
indispensable tools in modern organic synthesis. One of the major research goals in cross …

N-Sulfonyl hydrazones have been extensively used as operationally safe carbene
precursors in modern organic synthesis due to their ready availability, facile …

Lignin is a renewable and the most abundant aromatic source that can be used for extensive
chemicals and materials. Although approximately 50 million tons of lignin are produced …

Transition‐metal‐catalyzed reactions of N‐tosylhydrazones provide a convenient access to
various molecules by novel carbon‐carbon or carbon‐heteroatom bond formations via …

Palladium-catalyzed C–H functionalization of acyldiazomethanes with aryl iodides has been
developed. This reaction is featured by the retention of the diazo functionality in the …

A ligand controlled selective hydroborylation of alkynes to α-or β-vinylboronates has been
developed using a Pd catalyst. The high α-selectivity displayed by this reaction can be …

A diazo species is trapped in an intermolecular fashion by two independent ion species in
tandem at the carbene center to install an electrophile and a nucleophile on the same …

Palladium-Catalyzed Diarylmethyl C(sp3)–C(sp2) Bond Formation: A New Coupling Approach
toward Triarylmethanes | Organic Letters ACS ACS Publications C&EN CAS Find my institution …

Abstract'Diene'to know: The title reaction leads to the formation of 1, 3‐dienes in high yields
(see scheme). The reaction also proceeds with the use of N‐tosylhydrazone substrates …

Nickel-Catalyzed Direct Synthesis of Aryl Olefins from Ketones and Organoboron Reagents under
Neutral Conditions | Journal of the American Chemical Society ACS ACS Publications C&EN …