Marine organisms have proven to be rich sources of unique alkaloids. In earlier surveys we
comprehensively reviewed several intriguing groups of marine alkaloids, including the …

Covering: 2002. Previous review: Nat. Prod. Rep., 2003, 20, 1 This review covers the
literature published in 2002 for marine natural products, with 579 citations (413 for the …

The lamellarins form a group of more than 30 polyaromatic pyrrole alkaloids, isolated from
diverse marine organisms, mainly but not exclusively ascidians and sponges. These …

Pyrrole is one of the most important azaheterocycles, due to its wide range of applications in
pharmaceuticals and optoelectronic materials, coupled with its utility as an intermediate in …

Lamellarins are natural products isolated from marine invertebrates having a unique
heterocyclic ring system. Many of these natural products exhibit potentially useful biological …

Lamellarins are marine alkaloids containing fused 14-phenyl-6H-[1] benzopyrano [4′, 3′:
4, 5] pyrrolo [2, 1-a] isoquinoline or non-fused 3, 4-diarylpyrrole-2-carboxylate ring systems …

Lamellarins, a family of hexacyclic pyrrole alkaloids originally isolated from marine
invertebrates, display promising anti-tumor activity. They induce apoptotic cell death through …

The present review discusses the known synthetic routes to the lamellarin alkaloids
published until 2014. It begins with syntheses of the structurally simpler type-II lamellarins …

Total synthesis of cytotoxic marine alkaloids, lamellarins D, L, and N, has been achieved by
using Hinsberg-type pyrrole synthesis and palladium-catalyzed Suzuki–Miyaura coupling of …

Lamellarins are natural products with a [3, 4]-fused pyrrolocoumarin skeleton possessing
interesting biological properties. More than 70 members have been isolated from diverse …