Issue 8, 2022, Issue in Progress

Asymmetric total synthesis of four bioactive lignans using donor–acceptor cyclopropanes and bioassay of (−)- and (+)-niranthin against hepatitis B and influenza viruses

Abstract

The asymmetric total synthesis of four lignans, dimethylmatairesinol, matairesinol, (−)-niranthin, and (+)-niranthin has been achieved using reductive ring-opening of cyclopropanes. Moreover, we performed bioassays of the synthesized (+)- and (−)-niranthins using hepatitis B and influenza viruses, which revealed the relationship between the enantiomeric structure and the anti-viral activity of niranthin.

Graphical abstract: Asymmetric total synthesis of four bioactive lignans using donor–acceptor cyclopropanes and bioassay of (−)- and (+)-niranthin against hepatitis B and influenza viruses

Supplementary files

Article information

Article type
Paper
Submitted
24 Jan 2022
Accepted
31 Jan 2022
First published
07 Feb 2022
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2022,12, 4635-4639

Asymmetric total synthesis of four bioactive lignans using donor–acceptor cyclopropanes and bioassay of (−)- and (+)-niranthin against hepatitis B and influenza viruses

R. Ota, D. Karasawa, M. Oshima, K. Watashi, N. Shimasaki and Y. Nishii, RSC Adv., 2022, 12, 4635 DOI: 10.1039/D2RA00499B

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