Total synthesis of zyzzyanones A-D

Tetrahedron. 2013 May 20;69(20):4105-4113. doi: 10.1016/j.tet.2013.03.052.

Abstract

Zyzzyanones A-D is a group of biologically active marine alkaloids isolated from Australian marine sponge Zyzzya fuliginosa. They contain a unique bispyrroloquinone ring system as the core structure. The first total synthesis of all four zyzzyanones is described here. The synthesis of these alkaloids started from a previously known 6-benzylamino indole-4,7-quinone derivative and involves 6-7 steps. The key step in the synthesis involves the construction of a pyrrole ring in one step using a Mn(OAc)3 mediated oxidative free radical cyclization reaction of a 6-benzylamino indole-4,7-quinone derivative with 4-benzyloxyphenyl acetaldehyde diethyl acetal in CH3CN.

Keywords: Alkaloid; Marine; Mn(OAc)3; Quinone; Zyzzyanone.