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Regioselective synthesis of gentisyl alcohol-type marine natural products

  • School of Marine Science and Technology, Harbin Institute of Technology Weihai
  • CAS - Institute of Chemistry

Research output: Contribution to journalArticlepeer-review

Abstract

Gentisyl alcohol-type natural products, possessing various important biological properties, have been synthesized from 4-methoxyphenol by using a selective phenol monohydroxymethylation/monochlorination, a CAN oxidation and a sodium dithionite reduction as the key steps. The natural product synthesis is efficient, atom- and step-economical, and requires no protecting groups.

Original languageEnglish
Pages (from-to)1891-1896
Number of pages6
JournalNatural Product Research
Volume33
Issue number13
DOIs
StatePublished - 3 Jul 2019
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 14 - Life Below Water
    SDG 14 Life Below Water

Keywords

  • Natural products
  • chlorination
  • chlorogentisyl alcohol
  • gentisyl alcohol
  • hydroxymethylation
  • synthesis

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