930304-05-5Relevant articles and documents
A convergent total synthesis of the marine sponge alkaloid ageladine A via a strategic 6π-2-azatriene electrocyclization
Meketa, Matthew L.,Weinreb, Steven M.
, p. 9112 - 9119 (2008/02/09)
A second generation total synthesis of the marine sponge metabolite ageladine A utilizing a biogenetically inspired 6π-2-azaelectrocyclization of triene 34 as the key step is performed to construct the imidazopyridine core of the metabolite.
A new total synthesis of the zinc matrixmetalloproteinase inhibitor ageladine A featuring a biogenetically Patterned 6π-2-azatriene electrocyclization
Meketa, Matthew L.,Weinreb, Steven M.
, p. 853 - 855 (2007/10/03)
(Chemical Equation Presented) A convergent second generation total synthesis of the heterocyclic marine sponge metabolite ageladine A has been achieved by using a biomimetically inspired 6π-2-azatriene electrocyclization as the key step for formation of the imidazolopyridine moiety.