Synthetically-useful carbon-carbon and carbon-sulphur bond constructions mediated by carbon- and sulphur-centred radicals in water and aqueous media

AL POSTIGO *

ROYAL SOCIETY OF CHEMISTRY ADVANCES

ROYAL SOCIETY OF CHEMISTRY DOI:10.1039/C1RA00372K

Lugar: CHICHESTER- RSC Adv., 2011, DOI: 10.1039/C1RA00372K; Año: 2011 vol. 1 p. 14 - 32

1476-0576

This account is focused on carbon-carbon, and carbon-sulphur bond-forming reactions through the use of carbon- and sulphur-centred radicals in water, respectively. It intends to show the scope and applications on these types of radicals with a synthetic goal, thus helping the Radical Synthetic Chemist to grab the fundamental aspects devoted to the synthesis of a wide array of organic compounds through radical methods in environmentally friendly media. This account excludes the syntheses of organic substrates through the aid of organometallic / metal-centred radicals such as other Group IV-radicals and transition-metal radicals, and the important class of radical reductions currently accomplished in water through different metallic reducing species. The array of substrates synthesized through the present method encompasses intermolecular and intramolecular radical carbon-carbon bond formation reactions in water, and radical carbon-sulphur bond formation reactions. Among the radical carbon-carbon bond formation reactions, special attention is devoted to atom-transfer radical reactions, radical addition reactions to olefins, radical addition to carbon-nitrogen double bonds, and carboaminohydroxylation of alkenes, and the analogues of Knovonoegel reactions, synthesis of functionalized enol ethers, carboazidation and azidation, and ynol formation, and radical cyclization reactions in water.