Electricity-driven, oxidative C-H selenylative and tellurylative annulation of N-(2-alkynyl)anilines: sustainable synthesis of 3-selanyl/tellanylquinolines.

A metal- and oxidant-free, radical C-H selenylative and tellurylative annulation of N-(2-alkynyl)anilines with diorganyl dichalcogenides is developed under electrochemical conditions for the sustainable synthesis of valuable 3-selanyl/tellanylquinolines up to 92% yield at room temperature. The developed protocol required only electricity as the green reagent and offers high atom economy, broad substrate scope, and efficient scalability.

Iodine-Catalyzed Methylthiolative Annulation of 2-Alkynyl Biaryls with DMSO: A Metal-Free Approach to 9-Sulfenylphenanthrenes.

An iodine-catalyzed sustainable, cost-effective, and atom-economic synthetic methodology is developed to synthesize a wide variety of valuable sulfenylphenanthrenes and polycyclic heteroaromatics in moderate to high yield through electrophilic thiolative annulation of 2-alkynyl biaryls (6-endo-dig cyclization) using methyl sulfoxides such as dimethyl sulfoxide (DMSO) as the sulfur source under transition-metal-free conditions. The transformation requires only iodine in a catalytic amount and trifluoroacetic anhydride. Notably, DMSO played multiple roles such as methylthiolating reagent, oxidant, and solvent in this reaction.

Transition Metal- and Oxidant-Free Base-Mediated Selenation of Bicyclic Arenes at Room Temperature.

Bicyclic arenyl selenides are of much importance because of their pharmaceutical applications. A simple method for their synthesis has been developed by a reaction of 2-naphthol and styrenyl selenocyanate/diaryl diselenide in the presence of a base at room temperature. The selenation occurs exclusively at the 1-position of 2-naphthol unit. The reactions are relatively fast (2-4 h) and high yielding. A library of substituted naphthyl styrenyl and naphthyl aryl selenides are obtained by this procedure.

Organochlorine pesticide residues in sediments of a tropical mangrove estuary, India: implications for monitoring.

The paper examines the concentrations of isomers of hexachlorocyclohexane (HCHs), dichlorodiphenyl trichloroethane and its metabolites (DDTs), alpha-endosulfan and endosulfan sulfate in surface sediment samples collected from the mouth of Hugli estuary in the vicinity of Sundarban mangrove environment, eastern part of India. An overall pattern of accumulation of these pesticides was in the order of: SigmaHCH>endosulfan sulfate>SigmaDDT>alpha-endosulfan. The concentration of these compounds was quite low. An elevated level of SigmaHCH, SigmaDDT and endosulfan sulfate were marked during premonsoon months, a period characterized by high salinity and pH values. Among the isomers and metabolites of HCH and DDT, beta-HCH, pp'-DDT and pp'-DDE were found to be dominant. The sources of contamination are closely related to human activities, such as domestic and industrial discharges, agricultural chemical applications and soil erosion due to deforestation. The study is compared to other estuarine environment in India and abroad. The present data will serve as a baseline against which future anthropogenic effects may be assessed.