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Stereoselective Synthesis of Tetrahydrofuran Lignans

  • Mahidol University

Research output: Contribution to journalReview articlepeer-review

21 Citations (Scopus)

Abstract

This short review aims to summarize the reports on stereoselective synthesis of naturally occurring tetrahydrofuran lignans published during the period of 2006 to 2018. The stereoselective construction of non-natural tetrahydrofuran frameworks is not included in this review. 1 Introduction 2 Stereoselective Synthesis of 2,5-Diaryltetrahydrofuran (CL5-a) 2.1 Synthesis of CL5-a via Friedel-Crafts Arylation or Nucleophilic Addition/Reduction of γ-Butyrolactones 2.2 Synthesis of CL5-a via Intramolecular Cyclization of 1,4-Diarylbutanediols 2.3 Synthesis of CL5-a via Diastereoselective Hydrogenation of Furan Derivatives 2.4 Synthesis of CL5-a via Cycloaddition Reaction of Substituted Cyclopropane Derivatives 3 Stereoselective Synthesis of 2-Aryl-4-benzyltetrahydrofuran (CL5-b) 4 Stereoselective Synthesis of 3,4-Dibenzyltetrahydrofuran (CL5-c) 5 Conclusions.

Original languageEnglish
Article numbers-0037-1610289
Pages (from-to)4746-4764
Number of pages19
JournalSynthesis (Germany)
Volume50
Issue number24
DOIs
Publication statusPublished - 17 Dec 2018
Externally publishedYes

Keywords

  • bioactive compounds
  • furans
  • lignans
  • natural products
  • stereoselective synthesis

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