287920-04-1Relevant articles and documents
New synthesis of arcyriaflavin-A via silyl enol ether-mediated and Fischer indolisations
Alonso, Dulce,Caballero, Esther,Medarde, Manuel,Tomé, Fernando
, p. 4839 - 4841 (2005)
A new synthesis of the natural product arcyriaflavin-A is described. It was brought about through Diels-Alder cycloaddition and two indolisations based on silyl enol ether nucleophilic attack and Fischer processes.
New synthetic approach to arcyriaflavin-A and unsymmetrical analogs
Adeva, Marta,Buono, Frédéric,Caballero, Esther,Medarde, Manuel,Tomé, Fernando
, p. 832 - 834 (2007/10/03)
A new synthetic approach to the natural product arcyriaflavin-A and unsymmetrical analogs is described. The approach is based on successive Diels-Alder cycloaddition, Fischer indolization and formal nitrene insertion processes.