Total synthesis of avenaol
Avenaol is a potent germination stimulant that can be extracted from black oat. Here, the authors report the total synthesis of avenaol by developing a strategy to access all-cis-substituted cyclopropanes.
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| Format: | Article |
| Language: | English |
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Nature Publishing Group
2017-09-01
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| Series: | Nature Communications |
| Online Access: | https://doi.org/10.1038/s41467-017-00792-1 |
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doaj-26dcae8c6e71433abe85e260dda891ff |
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Article |
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doaj-26dcae8c6e71433abe85e260dda891ff2021-05-11T07:31:39ZengNature Publishing GroupNature Communications2041-17232017-09-01811910.1038/s41467-017-00792-1Total synthesis of avenaolMotohiro Yasui0Rina Ota1Chihiro Tsukano2Yoshiji Takemoto3Graduate School of Pharmaceutical Sciences, Kyoto UniversityGraduate School of Pharmaceutical Sciences, Kyoto UniversityGraduate School of Pharmaceutical Sciences, Kyoto UniversityGraduate School of Pharmaceutical Sciences, Kyoto UniversityAvenaol is a potent germination stimulant that can be extracted from black oat. Here, the authors report the total synthesis of avenaol by developing a strategy to access all-cis-substituted cyclopropanes.https://doi.org/10.1038/s41467-017-00792-1 |
| collection |
DOAJ |
| language |
English |
| format |
Article |
| sources |
DOAJ |
| author |
Motohiro Yasui Rina Ota Chihiro Tsukano Yoshiji Takemoto |
| spellingShingle |
Motohiro Yasui Rina Ota Chihiro Tsukano Yoshiji Takemoto Total synthesis of avenaol Nature Communications |
| author_facet |
Motohiro Yasui Rina Ota Chihiro Tsukano Yoshiji Takemoto |
| author_sort |
Motohiro Yasui |
| title |
Total synthesis of avenaol |
| title_short |
Total synthesis of avenaol |
| title_full |
Total synthesis of avenaol |
| title_fullStr |
Total synthesis of avenaol |
| title_full_unstemmed |
Total synthesis of avenaol |
| title_sort |
total synthesis of avenaol |
| publisher |
Nature Publishing Group |
| series |
Nature Communications |
| issn |
2041-1723 |
| publishDate |
2017-09-01 |
| description |
Avenaol is a potent germination stimulant that can be extracted from black oat. Here, the authors report the total synthesis of avenaol by developing a strategy to access all-cis-substituted cyclopropanes. |
| url |
https://doi.org/10.1038/s41467-017-00792-1 |
| work_keys_str_mv |
AT motohiroyasui totalsynthesisofavenaol AT rinaota totalsynthesisofavenaol AT chihirotsukano totalsynthesisofavenaol AT yoshijitakemoto totalsynthesisofavenaol |
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