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Review: [21 refs. [ABSTRACT FROM AUTHOR]

Review: 15 refs. [ABSTRACT FROM AUTHOR]

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

The procedure is successfully applied to the highly enantioselective transformation of aryl substituted allylamines. [ABSTRACT FROM AUTHOR]

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.

In the title reaction, DDQ serves as the oxidizing reagent as well as the hydrogen acceptor. [ABSTRACT FROM AUTHOR]

The title reaction completely omits the use of oxidant and base, producing hydrogen as the sole by-product. [ABSTRACT FROM AUTHOR]

The terphenyl products are obtained with high regioselectivity. [ABSTRACT FROM AUTHOR]

The article presents chemical equations related to the article "Pd(II)-Catalyzed C(sp²)-H Hydroxylation with R2(O)P-Coordinating Group" by H.-Y Zhang and other, published in the periodical "Organic Letters" in 2013.

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]