Stereoselective Synthesis of Tetrahydrofuran Lignans

Darunee Soorukram; Manat Pohmakotr; Chutima Kuhakarn; Vichai Reutrakul

doi:10.1055/s-0037-1610289

Synthesis, Inhaltsverzeichnis

Synthesis 2018; 50(24): 4746-4764
DOI: 10.1055/s-0037-1610289

short review

Stereoselective Synthesis of Tetrahydrofuran Lignans

Autor*innen

Darunee Soorukram*

Department of Chemistry and Center of Excellence for Innovation in Chemistry (PERCH-CIC), Faculty of Science, Mahidol University, Rama 6 Road, Bangkok 10400, Thailand eMail: darunee.soo@mahidol.ac.th
Manat Pohmakotr
Chutima Kuhakarn
Vichai Reutrakul

Abstract

Alle Artikel dieser Rubrik

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

Key words

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

Volltext

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