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DOI: 10.1055/s-0037-1610289
Stereoselective Synthesis of Tetrahydrofuran Lignans
The authors acknowledge financial support from the Thailand Research Fund (RSA6180025 and IRN58W0005), the Center of Excellence for Innovation in Chemistry (PERCH-CIC), and the Office of the Higher Education Commission and Mahidol University under the National Research Universities Initiative.Publication History
Received: 31 July 2018
Accepted after revision: 28 August 2018
Publication Date:
02 October 2018 (online)
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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
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For selected reviews on biosynthesis of lignans, see:
See, for example:
See, for example:
See, for example:
For a recent review, see:
See also:
See, for example:
See also:
For recent reviews, see:
See also:
See also:
For a recent review, see:
For recent reviews, see:
See, also: