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An abstract of the article "Visible-Light-Promoted Oxidative (4 + 2) Cycloadditions of Aryl Silyl Enol Ethers" by B. Yang and Z. Lu is presented.

An abstract of the article "Synthesis of 1,2-Diketones via a Metal-Free, Visible-Light-Induced Aerobic Photooxidation of Alkynes" by X. Liu, T. Cong, P. Liu and P. Sun is presented.

An abstract of the article "Visible-Light Induced Oxidant-Free Oxidative Cross-Coupling for Constructing Allylic Sulfones from O lefins and Sulfinic Acids" by authors including Lingling Zhang, Hong Yi, and Yi Luo.

An abstract of the article "N-Hydroxyphthalimide: A New Photoredox Catalyst for (4 + 1) Radical Cyclization of N-Methylanilines with Isocyanides" by A. K. Yadav and L. D. S. Yadav is presented.

The reaction of α-keto acids with carbodiimides provides O-acyl urea intermediates which undergo visible light induced rearrangement to form unexpected hydantoine derivatives. [ABSTRACT FROM AUTHOR]

An abstract of the article "Visible-Light Photoredox-Catalyzed Coupling Reaction of Azoles with α-Carbamoyl Sulfides" by Lucie Jarrige, Guillaume Levitre, and Géraldine Masson is presented.

An abstract of the article "High Diastereoselectivity in the Yang Photocyclization via Remote Hydrogen Abstraction Reaction" by M. Jang and B. S. Park is presented.

The title reaction between acetophenone derivatives and benzylamines delivers various 2,4,6-trisubstituted pyridines moderate to high yields. [ABSTRACT FROM AUTHOR]

An abstract of the article "Visible-Light-Induced Trifluoromethylation of Isonitrile-Substituted Methylenecyclopropanes: Facile Access to 6-(Trifluoromethyl)-7,8-dihydrobenzo k phenanthridine Derivatives" by X.-B. Hu, Y. Wei and M. Shi is presented.

The scalable method represents a mild, environmentally benign access to 1,3-oxazin-6-ones. [ABSTRACT FROM AUTHOR]

Review: 252 refs. [ABSTRACT FROM AUTHOR]

Review: photophysical properties; 190 refs. [ABSTRACT FROM AUTHOR]

Review: 631 refs. [ABSTRACT FROM AUTHOR]

An abstract of the article "Visible-Light Photoredox-Catalyzed Coupling Reaction of Azoles with α-Carbamoyl Sulfides" by Lucie Jarrige, Geraldine Masson and colleagues is presented.

Review: 252 refs. [ABSTRACT FROM AUTHOR]

The article presents chemical equations for the article "Broensted Acid Cocatalysis in Photocatalytic Intramolecular Coupling of Tertiary Amines: Efficient Synthesis of 2-Arylindols" by X. Yuan and colleagues published in "Organic and Biomolecular Chemistry" in 2016.

Two new photocatalytic systems based on flavinium species formed in situ by protonation of riboflavin-tetraacetate or prepared in advance via alloxazine quaternization are used as tools for the title reaction. [ABSTRACT FROM AUTHOR]

Using photo-excited 4-benzoylpyridine as sensitizer and p-anisylsulfonyl oxime as an aldoxime precursor, the chemoselective introduction of the aldoxime functional group into various substrates is achieved. [ABSTRACT FROM AUTHOR]

Chemical equations are presented for the article "Bismuth(III) Triflate-Catalyzed Tandem Cyclizations Towards Complex Polycyclic Ethers" by P. Ondet and colleagues, published in the periodical "Organic Chemistry Frontiers."

The title reaction with electron-deficient olefins proceeds with excellent regio-, diastereo-, and enantioselectivity and is applicable to isoquinolones. [ABSTRACT FROM AUTHOR]

Review: 53 refs. [ABSTRACT FROM AUTHOR]

Review: 358 refs. [ABSTRACT FROM AUTHOR]

Blue LEDs as light source and Ir complex IPB as photocatalyst mediated cross-coupling between tertiary amines possessing an N-methyl or N-methylene group and geminal difluoroalkenes to give the C(sp3)-fluoroalkenylated products in modest to high yields. [ABSTRACT FROM AUTHOR]

The title reaction is achieved in the presence of a typical iridium photocatalyst and various substrates are tolerable. [ABSTRACT FROM AUTHOR]

The synthesis of a wide range of functionalized phthalazine derivatives from sulfonylhydrazone precursors under mild photoredox conditions is presented. [ABSTRACT FROM AUTHOR]

Chemical equations for the article "Synthesis of Trifluoromethylated 3,4-Dihydroquinolin-2(1H)-ones via a Photo--Induced Radical Cyclization of Benzene-Tethered 1,7-Enynes with Togni Reagent" by Y. An, appeared in the periodical "Organic Chemistry Frontiers" is presented.

A novel approach to biaryl sultams by photo-induced denitrogenative cyclization of 1,2,3,4-benzothiatriazine-1,1-dioxides is developed. [ABSTRACT FROM AUTHOR]

Review: 50 refs. [ABSTRACT FROM AUTHOR]

Review: 173 refs. [ABSTRACT FROM AUTHOR]

The article presents chemical equations for an article "Decarboxylative anti-Michael Addition to Olefins Mediated by Photoredox Catalysis" by G.H. Lovett and others, which appeared in 2016 issue of journal "Organic Letters."

Utilizing an organic photocatalyst, aminodecarboxylation of unactivated alkanecarboxylic acids generates reactive alkyl radical intermediates, which are trapped with azodicarboxylate to provide alkylated hydrazinedicarboxylates. [ABSTRACT FROM AUTHOR]

The highly regioselective one-pot synthesis of oxathioles is promoted by visible light using eosin Y as organophotoredox catalyst and air as sustainable reagent. [ABSTRACT FROM AUTHOR]

The fluorescence properties of the products are examined. [ABSTRACT FROM AUTHOR]

The article presents chemical equations for the article "Visible-Light-Promoted Direct Amination of Phenols via Oxidative Cross-Dehydrogenative Coupling Reaction" by Y. Zhao and others, published in "Organic Letters" in 2016.

The article presents chemical equations for the article "Synthesis of Aryl Trimethylstannanes from Aryl Halides: An Efficient Photochemical Method", by K. Chen and others, published in "Chemical Communications" in 2016.

The formation of the title compounds is carried out in a two-chambered system: first, an alkyl radical is generated which subsequently is subjected to aminocarbonylation, where CO is released from molybdenum hexacarbonyl. [ABSTRACT FROM AUTHOR]

Diagrams of chemical reactions of adipic acid active esters coupling through consecutive visible-light photoredox cecarboxylative along with the use of alkynyl sulfones leading to cyclic compound or cyclopentane derivatives is presented.

A thiyl-radical-catalyzed cyclization reaction of N-tosyl vinylaziridines and alkenes is developed as a new synthetic method for the generation of substituted pyrrolidines. [ABSTRACT FROM AUTHOR]

The title coumarins are obtained under sunlight via a cascade of radical iodination, spirocyclization, and ring expansion through ester migration affording the kinetically favoured product. [ABSTRACT FROM AUTHOR]

The annulation of N-(2-bromophenyl)pyrroles (I) with arylalkynes (II) gives rise to desired pyrrolo[1,2-a]quinolines (III). [ABSTRACT FROM AUTHOR]

Review: 540 refs. [ABSTRACT FROM AUTHOR]

Review: 83 refs. [ABSTRACT FROM AUTHOR]

Review: 59 refs. [ABSTRACT FROM AUTHOR]

Review: 579 refs. [ABSTRACT FROM AUTHOR]

Review: 546 refs. [ABSTRACT FROM AUTHOR]

Review: 485 refs. [ABSTRACT FROM AUTHOR]

Review: 853 refs. [ABSTRACT FROM AUTHOR]

The method allows the oxidation of primary and secondary alcohols as well as allylic alcohols to the corresponding carbonyl compounds. [ABSTRACT FROM AUTHOR]

The scalable, robust, and catalyst-free method has a broad substrate scope, thus offering access to a broad range of styrene derivatives, α,β-unsaturated carbonyl compounds as well as 1,2 and 1,2-disubstituted and even trisubstituted alkenes, including cyclic ones. [ABSTRACT FROM AUTHOR]

The reaction has a broad substrate scope, thus tolerating diversely functionalized styrene derivatives as well as cyclic and acyclic internal alkenes and various N-arylated bromodifluoroacetamides, but no N-alkylated derivatives thereof. [ABSTRACT FROM AUTHOR]