RESUMO
Organocatalysis-catalysis mediated by small chiral organic molecules-is a powerful technology for enantioselective synthesis, and has extensive applications in traditional ionic, two-electron-pair reactivity domains. Recently, organocatalysis has been successfully combined with photochemical reactivity to unlock previously inaccessible reaction pathways, thereby creating new synthetic opportunities. Here we describe the historical context, scientific reasoning and landmark discoveries that were essential in expanding the functions of organocatalysis to include one-electron-mediated chemistry and excited-state reactivity.
Assuntos
Técnicas de Química Sintética/métodos , Química Orgânica/métodos , Fotoquímica/métodos , Catálise/efeitos da radiação , Coenzimas/metabolismo , Coenzimas/efeitos da radiação , Elétrons , Oxirredução/efeitos da radiação , EstereoisomerismoAssuntos
Coenzimas/química , Guanosina Monofosfato/análogos & derivados , Methanobacteriaceae/enzimologia , Oxirredutases atuantes sobre Doadores de Grupo CH-NH/química , Cromatografia Líquida de Alta Pressão , Coenzimas/metabolismo , Coenzimas/efeitos da radiação , Guanosina/análise , Guanosina/química , Guanosina Monofosfato/química , Espectroscopia de Ressonância Magnética , Espectrometria de Massas , Peso Molecular , Diester Fosfórico Hidrolases/metabolismo , Piridonas/química , Espectrofotometria Ultravioleta , Raios UltravioletaAssuntos
Antagonistas Adrenérgicos alfa/farmacologia , Antagonistas Adrenérgicos beta/farmacologia , Coenzimas/efeitos da radiação , Piridoxal/efeitos da radiação , Animais , Encéfalo/efeitos da radiação , Coração/efeitos da radiação , Técnicas In Vitro , Fígado/efeitos da radiação , Compostos Organofosforados/efeitos da radiação , Fosfato de Piridoxal/efeitos da radiação , Piridoxamina/análogos & derivados , Piridoxamina/efeitos da radiação , Ratos , Ratos EndogâmicosRESUMO
The yields of inorganic phosphate from irradiated phosphate esters of biological interest have been measured in the presence of various free-radical scavengers. These studies indicate that hydroxyl radical attack on the phosphate esters accounts for most of this damage. Competition kinetics using different hydroxyl radical scavengers whose reactivities are known have been used to estimate the rate-constants for the overall hydroxyl radical reactivities of the phosphate esters. The extent of hydroxyl-radical-induced dephosphorylation is very low for nucleotide derivatives, but high for some sugar and glycerol phosphates, reflecting the probability of hydroxyl radical abstraction at the alpha or beta carbon atoms adjacent to the phosphate ester linkage. The hydroxyl radical reactivities of nucleotides, coenzymes, sugar phosphates and phospholipid components are all high (1-10 X 10(9) M-1 sec-1), indicating the importance of hydroxyl radical attack in the inactivation of these components in living cells, although not necessarily by dephosphorylation.