A convergent total synthesis of the marine sponge alkaloid ageladine A via a strategic 6π-2-azatriene electrocyclization
摘要:
A second generation total synthesis of the marine sponge metabolite ageladine A utilizing a biogenetically inspired 6 pi-2-azaelectrocyclization of triene 34 as the key step is performed to construct the imidazopyridine core of the metabolite. (c) 2007 Elsevier Ltd. All rights reserved.
A New Total Synthesis of the Zinc Matrixmetalloproteinase Inhibitor Ageladine A Featuring a Biogenetically Patterned 6π-2-Azatriene Electrocyclization
摘要:
A convergent second generation total synthesis of the heterocyclic marine sponge metabolite ageladine A has been achieved by using a biomimetically inspired 6 pi 2-azatriene electrocyclization as the key step for formation of the imidazolopyridine moiety.