Tyrosine Alkaloids

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

Abstract

Tyrosine serves as substrate for the biosynthesis of a variety of structurally diverse natural products, and some of these secondary metabolites are of great pharmacologic, historic, and economic importance. This chapter provides an overview of the most important biosynthetic pathways leading to tyrosine alkaloids. It outlines the synthetic approaches toward members of this class of secondary metabolites, mainly tetrahydroisoquinoline alkaloids and opiates. The focus is on biosynthetic routes and biomimetic synthesis. The chapter discusses various methods that have been elaborated to allow the formation of aryl-aryl bonds. Additionally, the chemical syntheses described within the chapter have also been chosen in such a way as to present and discuss interesting strategies for the crucial aryl-aryl coupling reaction. These natural products have played an important role in the development of oxidative coupling protocols as well as transition metal-catalyzed procedures.

Original languageEnglish
Title of host publicationFrom Biosynthesis to Total Synthesis
Subtitle of host publicationStrategies and Tactics for Natural Products
PublisherWiley-Blackwell
Pages431-472
Number of pages42
ISBN (Electronic)9781118754085
ISBN (Print)9781118751732
DOIs
Publication statusPublished - 3 Apr 2016
Externally publishedYes

UN SDGs

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

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Aryl-aryl coupling reactions
  • Biosynthesis
  • Opiates
  • Secondary metabolites
  • Tetrahydroisoquinoline alkaloids
  • Tyrosine alkaloids

Research fields

  • Alkaloids
  • Total Synthesis

IMC Research Focuses

  • Materials science

ÖFOS 2012 - Austrian Fields of Study

  • 104015 Organic chemistry

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