Hypervalent iodine (HVI) chemistry is a rapidly growing subdomain of contemporary organic
chemistry because of its enormous synthetic applications. The high nucleofugality of the …

Presently, the major cornerstone of the research community is to develop green as well as
sustainable protocols involving inexpensive catalysts and/or reagents without the usage of …

Oxy‐/amino‐difluoromethylthiolation of β, γ‐unsaturated oximes/hydrazones have been
developed for construction of HCF2S‐containing isoxazolines and pyrazolines by employing …

Efficient enantioselective synthesis of pyrazolines and isoxazolines enabled by an iridium-catalyzed
intramolecular allylic substitution reaction - Organic Chemistry Frontiers (RSC Publishing) …

Halogens play a crucial part in synthetic organic chemistry. Halo‐cyclized products hold
numerous applications in the pharmaceutical industries, agrochemicals, natural product …

Acylation of nitroalkylmalonates was found to yield substituted isoxazoline derivatives. This
redox‐neutral transformation has a wide substrate scope and produces target products with …

Heterocycles are a valuable type of structural motifs which occupy a major space in the area
of medicinal, pharmaceutical, and bioactive natural product chemistry as well as synthetic …

Bridged polycyclic molecular skeletons and related systems are key structural motifs in
medicinal chemistry. The most efficient and widely accepted method for the syntheses of the …

Many targeted natural product isolation approaches rely on the use of pre-existing bioactivity
information to inform the strategy used for the isolation of new bioactive compounds …

An electrochemical method for the green and practical synthesis of a broad range of
substituted isoxazoline cores is presented. Both aryl and more challenging alkyl aldoximes …