Literature DB >> 28737179

Total synthesis of the dictyodendrins as an arena to highlight emerging synthetic technologies.

Wenhan Zhang1, Joseph M Ready.   

Abstract

Covering: 1993-2017This review discusses the isolation, biological activity, and syntheses of the dictyodendrin class of natural products, covering the years 1993-2017. The dictyodendrins are a family of alkaloids isolated from marine sponges, Dictyodendrilla verongiformis and Ianthella sp., which possess a highly substituted pyrrolo[2,3-c]carbazole core at the phenol or quinone oxidation states. Dictyodendrins exhibit a wide range of biological activities, such as telomerase inhibition, BACE1 enzyme inhibition, and cytotoxicity against several cancer cell lines. The unique structure and interesting biological activities of dictyodendrins provided a platform for the application of novel synthetic methods including C-H insertion, C-H arylation, and electrocyclization cascades.

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Year:  2017        PMID: 28737179     DOI: 10.1039/c7np00018a

Source DB:  PubMed          Journal:  Nat Prod Rep        ISSN: 0265-0568            Impact factor:   13.423


  3 in total

Review 1.  Marine Pyrrole Alkaloids.

Authors:  Kevin Seipp; Leander Geske; Till Opatz
Journal:  Mar Drugs       Date:  2021-09-10       Impact factor: 5.118

2.  Sequential Annulations to Interesting Novel Pyrrolo[3,2-c]carbazoles.

Authors:  Alice Benzi; Lara Bianchi; Massimo Maccagno; Angela Pagano; Giovanni Petrillo; Cinzia Tavani
Journal:  Molecules       Date:  2019-10-22       Impact factor: 4.411

Review 3.  Recent Advances in Construction of Polycyclic Natural Product Scaffolds via One-Pot Reactions Involving Alkyne Annulation.

Authors:  Liyao Zheng; Ruimao Hua
Journal:  Front Chem       Date:  2020-10-15       Impact factor: 5.221

  3 in total

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