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 language | English |
|---|---|
| Article number | s-0037-1610289 |
| Pages (from-to) | 4746-4764 |
| Number of pages | 19 |
| Journal | Synthesis (Germany) |
| Volume | 50 |
| Issue number | 24 |
| DOIs | |
| Publication status | Published - 17 Dec 2018 |
| Externally published | Yes |
Keywords
- bioactive compounds
- furans
- lignans
- natural products
- stereoselective synthesis
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