Abstract

Oceans have shown to be a remarkable source of natural products. The biological properties of many of these compounds have helped to produce great advances in medicinal chemistry. Within them, marine natural products containing an oxepanyl ring are present in a great variety of algae, sponges, fungus and corals and show very important biological activities, many of them possessing remarkable cytotoxic properties against a wide range of cancer cell lines. Their rich chemical structures have attracted the attention of many researchers who have reported interesting synthetic approaches to these targets. This review covers the most prominent examples of these types of compounds, focusing the discussion on the isolation, structure determination, medicinal properties and total synthesis of these products.

Highlights

  • More than 70% of Earth surface is covered by water, 96.5% of which is found in the oceans.This means that the planet’s largest habitat is the ocean, which is the ecosystem where the major part of animals and plants of Earth lives

  • Aplysistatin was first isolated from the South Pacific Ocean sea hare Aplysia angasi in 1977 [8]

  • Their an alternative route based on the formation the12-hydroxypalisadin oxepanyl derivative systems, andstrategy appliedfollowed it to the synthesis of aplysistatin, palisadins

Read more

Summary

Introduction

More than 70% of Earth surface is covered by water, 96.5% of which is found in the oceans. Natural products containing an oxepanyl moiety have been frequently found in sponges, corals, or different marine fungus, within others Their interesting biological properties include anticancer, antibacterial or antifungal activities. We B could mention manysubstances other families and examples of marine natural products that bear the oxepane moiety (spiroxins, phomactins, clavulazols, etc.) but review. Some isolated examples of the compounds described hereother are present in otherexamples reviews devoted to marine described triterpeneshere [6] or marine natural work. Some isolated of the compounds are present in described here are present in other reviews devoted to marine triterpenes [6] or marine natural products [7].

Halogenated Sesquiterpenoids
Structure of 5β-hydroxypalisadin
Overview
Couladouros’
Marine Diterpenes
Marine
Sipholenols Family
Neviotanes and Dahabanes
Sodwanones
Shaagrockols
Raspacionins
Meroterpenoids: Meroterpenoids
Retrosynthetic
43. This compound dimethylated to furnish
Second
Bromotyrosine Alkaloids
12. Psammaplysins
Guanidinium
70. A second of the the hydroxyl
Summarized
10. Alternative synthesis developed by Murphy towards Crambescidin
Oxepinamides
16. Ittoisthe worth that Oxepinamide
12. Retrosynthetic
95. Resulting
18. Protuboxepins
Diketopiperazine
21. Emestrin
22. Structures
16. Retrosynthetic
Findings
19. Retrosynthetic
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call