Total syntheses of shizukaols A and E
Shizukaols, bioactive dimers naturally occurring in the Chloranthaceae family, possess a complex polycyclic framework with more than ten contiguous stereocenters. Here the authors report the total syntheses of shizukaols A and E achieved via a modified Diels–Alder reaction mimicking the biosynthetic...
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Format: | Article |
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Nature Portfolio
2018-10-01
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Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-018-06245-7 |
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author | Jian-Li Wu Yin-Suo Lu Bencan Tang Xiao-Shui Peng |
author_facet | Jian-Li Wu Yin-Suo Lu Bencan Tang Xiao-Shui Peng |
author_sort | Jian-Li Wu |
collection | DOAJ |
description | Shizukaols, bioactive dimers naturally occurring in the Chloranthaceae family, possess a complex polycyclic framework with more than ten contiguous stereocenters. Here the authors report the total syntheses of shizukaols A and E achieved via a modified Diels–Alder reaction mimicking the biosynthetic pathway. |
first_indexed | 2024-12-21T08:02:42Z |
format | Article |
id | doaj.art-d6608fe0878048248a3f11a12a24dd56 |
institution | Directory Open Access Journal |
issn | 2041-1723 |
language | English |
last_indexed | 2024-12-21T08:02:42Z |
publishDate | 2018-10-01 |
publisher | Nature Portfolio |
record_format | Article |
series | Nature Communications |
spelling | doaj.art-d6608fe0878048248a3f11a12a24dd562022-12-21T19:10:52ZengNature PortfolioNature Communications2041-17232018-10-01911710.1038/s41467-018-06245-7Total syntheses of shizukaols A and EJian-Li Wu0Yin-Suo Lu1Bencan Tang2Xiao-Shui Peng3Department of Chemistry, and State Key Laboratory of Synthetic Chemistry, The Chinese University of Hong KongDepartment of Chemistry, and State Key Laboratory of Synthetic Chemistry, The Chinese University of Hong KongDepartment of Chemical and Environmental Engineering, The University of Nottingham Ningbo ChinaDepartment of Chemistry, and State Key Laboratory of Synthetic Chemistry, The Chinese University of Hong KongShizukaols, bioactive dimers naturally occurring in the Chloranthaceae family, possess a complex polycyclic framework with more than ten contiguous stereocenters. Here the authors report the total syntheses of shizukaols A and E achieved via a modified Diels–Alder reaction mimicking the biosynthetic pathway.https://doi.org/10.1038/s41467-018-06245-7 |
spellingShingle | Jian-Li Wu Yin-Suo Lu Bencan Tang Xiao-Shui Peng Total syntheses of shizukaols A and E Nature Communications |
title | Total syntheses of shizukaols A and E |
title_full | Total syntheses of shizukaols A and E |
title_fullStr | Total syntheses of shizukaols A and E |
title_full_unstemmed | Total syntheses of shizukaols A and E |
title_short | Total syntheses of shizukaols A and E |
title_sort | total syntheses of shizukaols a and e |
url | https://doi.org/10.1038/s41467-018-06245-7 |
work_keys_str_mv | AT jianliwu totalsynthesesofshizukaolsaande AT yinsuolu totalsynthesesofshizukaolsaande AT bencantang totalsynthesesofshizukaolsaande AT xiaoshuipeng totalsynthesesofshizukaolsaande |