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A promoter‐free chalcogenophosphorylation reaction between diverse P(O)−H reagents and chalcogenosulfonates has been developed. In the absence of metal or any other additives, these transformations proceed through a spontaneous process at room temperature, which provide a convenient and compatible approach to a broad range of selenophosphates and thiophosphates. [ABSTRACT FROM AUTHOR]

A TFAA/DMSO/NaF‐based system for the efficient fluorination of P(O)−H and P(O)−OH compounds has been developed. Without adding highly toxic and expensive fluorination reagents, this novel transformation provides direct and compatible access to a variety of fluorophosphonates and phosphonofluoridates in a one‐pot manner. [ABSTRACT FROM AUTHOR]

A Cerium(IV)‐promoted phosphinoylation‐nitratation of alkenes is established under mild conditions. In this process, Ceric ammonium nitrate (CAN) acts as a cheap phosphorus‐radical initiator, as well as a nitrate donor. Various β‐nitrooxyphosphonates are delivered in high yield in a one‐pot manner. [ABSTRACT FROM AUTHOR]

Phosphonation of various alkenes furnishes regio- and stereoselectively allyl phosphorylated products under mild conditions. [ABSTRACT FROM AUTHOR]

Abstract: A novel metal-free oxidative arylphosphination of activated N-substituted-N-arylacrylamide derivatives by phosphorylation and C–H functionalization cascade process has been developed. This methodology provides an efficient way to construct a variety of phosphorus-containing oxindole moieties. [Copyright &y& Elsevier]

Title compounds (III) and (V) are prepared by a Cu-catalyzed amino-phosphorous difunctionalization via cascade cyclization. [ABSTRACT FROM AUTHOR]

This novel and efficient method furnishes alkenylphosphine oxides in moderate to good yields. [ABSTRACT FROM AUTHOR]

The article presents chemical equations related to the article "Convenient Formation of Triarylphosphines by Nickel-Catalyzed C-P Cross-Coupling with Aryl Chlorides." by M. Sun and others, published in the periodical "European Journal of Organic Chemistry" in 2014.

A simple process for the Cu(II)-catalyzed oxidative phosphonation of α-amino-carbonyl compounds to yield imidoylphosphonates is described. [ABSTRACT FROM AUTHOR]

The article presents a chemical diagram which shows the direct annulations for phosphorylated oxindoles with carbon-phosphorus functionalization of alkenes catalyzed by silver.

Various diphenylphosphoryl compounds (III) and (V) are prepared using a simple and mild method. [ABSTRACT FROM AUTHOR]