Recent discoveries on the structure of iodine( iii ) reagents and their use in cross-nucleophile
coupling - Chemical Science (RSC Publishing) DOI:10.1039/D0SC03266B Royal Society of …

Nowadays, hypervalent iodine chemistry has remarkably advanced in parallel with the
emergence of novel hypervalent iodine reagents. Hypervalent iodine reagents, due to their …

The construction of 2-amino-1, 3-selenazole skeleton was realized via the PhICl2/KSeCN-
enabled electrophilic selenocyanation of β-enaminones and β-enamino esters followed by …

Pnictogen‐bonding catalysis and supramolecular σ‐hole catalysis in general is currently
being introduced as the non‐covalent counterpart of covalent Lewis acid catalysis. With …

The chemistry of hypervalent iodine reagents has emerged as an astonishing field in
synthetic organic chemistry owing to its easy availability and benign environmental features …

Perovskite solar cells (PSCs) have achieved tremendous success in advancing high power
conversion efficiencies. However, defect-induced recombination at grain boundaries (GBs) …

The existing hypervalent I (III) reagents bearing ONO2 group are limited in types and their
applications primarily focused on the nitrooxylation reactions featuring a fully-exo fashion …

ortho -Nitro-substituted diaryliodonium salts enabled regioselective cyclization of arylcarboxylic
acids toward 3,4-naphthocoumarins - Organic & Biomolecular Chemistry (RSC Publishing) …

Diazomethyl‐substituted iodine (III) compounds with electron‐withdrawing groups (EWG)
connected to diazo methyl center were a type of donor‐acceptor diazo compounds with …

Azirine Weinreb amides (N-methoxy-N-methyl-2H-azirine-2-carboxamides) were
synthesized in yields of 35–94% by the reaction of N, O-dimethylhydroxylamine with 2H …