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A palladium-catalyzed, temporary P(O) directing group assisted C–H bond arylation of carbazoles was achieved. The release of the directing group occurs spontaneously in the reaction and the mechanistic studies indicate that acid is essential for N–P bond cleavage. [ABSTRACT FROM AUTHOR]

Highly selective arylation catalyzed by palladium and directed by the acetamino group provides an efficient and practical protocol for constructing unique biaryl scaffolds, which could be further transformed into different structural units found in a range of natural products. 1 Introduction 2 Highly Regioselective Halogenation 3 Highly Regioselective Arylation 3.1 With Arylboronic Acids 3.2 With Trialkoxyarylsilanes 3.3 With Simple Arenes 3.4 Further Transformations 4 Conclusion [ABSTRACT FROM AUTHOR]

Arylacrylamides (I), (IV), and (VI) are found to react with aryl bromides and benzyl chloride in the presence of a Rh-catalyst to yield oxindoles. [ABSTRACT FROM AUTHOR]

Review: 15 refs. [ABSTRACT FROM AUTHOR]

A diagram is presented which explains the carbonitration of the chemical compound acrylamides for the nitrating oxindoles synthesis.

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

This oxidative arylation is suitable for a variety of α-amino acid derivatives, e.g. esters and amides including peptides. [ABSTRACT FROM AUTHOR]

The title reaction represents the first example of an aldehyde directly participating in the intramolecular Friedel-Crafts alkylation reaction. [ABSTRACT FROM AUTHOR]

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

A one-pot tandem allylic C-H activation/dearomatization reaction sequence between indole derivatives and allylarenes provides 3-arylpropenyl substituted indolenines in often high yields. [ABSTRACT FROM AUTHOR]

2-Methylpyridine, 3- and 4-methylquinolines give only trace amounts of the desired product or fail in the reaction. [ABSTRACT FROM AUTHOR]

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

Although the transformation succeeds efficiently for indole system the reaction fails for pyrroles. [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.

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

The article presents chemical reactions related to an article "Palladium-Catalyzed sp² and sp³ C—H Bond Activation and Addition to Isatin Toward 3-Hydroxy-2-oxindoles" by W. G. Wang and colleagues which appeared in a 2013 issue of the periodical "Organic Letters".

The article presents chemical reactions related to an article "Pd(II)-Catalyzed Ph 2 (O)P-Directed C—H Olefination Toward Phosphine—Alkene Ligands" by L. H. Wang and colleagues in a 2013 issue of the periodical "Organic Letters".

The silver-catalyzed carboazidation of alkenes and a subsequent CH-functionalization cascade process allows the synthesis of a wide range of azide oxindoles. [ABSTRACT FROM AUTHOR]

The title reaction allows the synthesis of various quinoline derivatives. [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.