Volume II describes 17 additional functional groups and presents a critical review of their
available methods of synthesis with preparative examples of each. Attention is especially …

The article offers information on the recent developments in flavin-based catalysis. It informs
that flavins can be excited by irradiation with the help of visible light which makes them …

The reduction of a double bond in the presence of hydrazine appears to have been first
observed in 1905 during the reaction of glyceryl oleate, which produced stearic hydrazide …

The use of acyl hydrazines (hydrazides) as precursors for the stoichiometric generation of
acyl radicals is explored. Two classes of substrates are examined: unsubstituted acyl …

A versatile reducing agent, diimide, can be generated efficiently by the aerobic oxidation of
hydrazine with neutral and cationic synthetic flavin catalysts 1 and 2. This technique …

Cyclic seleninate esters serve as catalysts for the rapid oxidation of sulfides to sulfoxides,
alkenes to epoxides, and enamines to α-hydroxyketones. Optimal conditions were found that …

Rongalite® promotes cleavage of diaryl disulfides generating chalcogenolate anions that
then undergo facile acylation with anhydrides in the presence of CsF to afford thioesters (3) …

Synthesis of Thiol, Selenol, and Tellurol Esters by the Reaction of Organochalcogeno Mercurials
with Acid Chlorides | Organometallics Recently Viewedclose modal ACS ACS Publications C&EN …

This article describes an efficient and easy one-pot route for the synthesis of a wide range of
selenol esters from acyl chloride with diselenides in the presence of indium metal. A variety …

The glutathione peroxidase-like catalysis of α-(phenylselenenyl) ketones was investigated.
Degradation studies demonstrated the rapid cleavage of the aliphatic carbon-selenium bond …