Cylindricines, lepadiformine, and fasicularin are marine alkaloids with a common novel pyrrolo- and pyrido[1,2-j]quinoline skeleton. They have recently been isolated from various tunicates and have shown interesting cytotoxic effects which could be attributed to covalent interactions with DNA, as well as cardiovascular effects. The promising biological activities together with the unique structural features make these alkaloids interesting targets for natural product synthesis. This review focuses on the different approaches developed for their synthesis with a particular emphasis on the key step where the quaternary amino substituted carbon center is created
Detailed chemical examination of the alkaloid content of an ascidian (Clavelina cylindrica) and two ...
Interesting biological activity has been ascribed to many natural products containing multi-substitu...
A marine natural product possesses a diverse and unique scaffold that contributes to a vast array of...
Cylindricines, lepadiformines, and fasicularin are tricyclic marine alkaloids bearing perhydropyrrol...
This thesis is divided into four chapters. The first chapter comprises an introduction to the fasicu...
The structures, origins, biogenesis, synthesis and bioactivity of a selection of N-heterocyclic mari...
Marine tricyclic alkaloids lepadiformine and fasicularin, with a unique perhydropyrrolo[2,1-j]quin...
Secondary metabolites from marine organisms are a rich source of novel leads for drug development. A...
In this review the marine derived decahydroquinoline alkaloid chemistry and biology is described. A ...
We describe here the diastereocontrolled formal racemic syntheses of tricyclic marine alkaloids, lep...
The present review describes research on novel natural antitumor alkaloids isolated from marine inve...
Drug discovery is reliant on new developments in natural product chemistry as well as advances in ch...
Chiral amino alcohol derived lactams are a valuable scaffold for the enantioselective synthesis of a...
A cross-metathesis protocol has been developed to provide facile access to highly hindered trisubsti...
Herein is described an original approach to access a tricyclic framework of the lepadiformine-type a...
Detailed chemical examination of the alkaloid content of an ascidian (Clavelina cylindrica) and two ...
Interesting biological activity has been ascribed to many natural products containing multi-substitu...
A marine natural product possesses a diverse and unique scaffold that contributes to a vast array of...
Cylindricines, lepadiformines, and fasicularin are tricyclic marine alkaloids bearing perhydropyrrol...
This thesis is divided into four chapters. The first chapter comprises an introduction to the fasicu...
The structures, origins, biogenesis, synthesis and bioactivity of a selection of N-heterocyclic mari...
Marine tricyclic alkaloids lepadiformine and fasicularin, with a unique perhydropyrrolo[2,1-j]quin...
Secondary metabolites from marine organisms are a rich source of novel leads for drug development. A...
In this review the marine derived decahydroquinoline alkaloid chemistry and biology is described. A ...
We describe here the diastereocontrolled formal racemic syntheses of tricyclic marine alkaloids, lep...
The present review describes research on novel natural antitumor alkaloids isolated from marine inve...
Drug discovery is reliant on new developments in natural product chemistry as well as advances in ch...
Chiral amino alcohol derived lactams are a valuable scaffold for the enantioselective synthesis of a...
A cross-metathesis protocol has been developed to provide facile access to highly hindered trisubsti...
Herein is described an original approach to access a tricyclic framework of the lepadiformine-type a...
Detailed chemical examination of the alkaloid content of an ascidian (Clavelina cylindrica) and two ...
Interesting biological activity has been ascribed to many natural products containing multi-substitu...
A marine natural product possesses a diverse and unique scaffold that contributes to a vast array of...