Syntheses of methylenolactocin and nephrosterinic acid via diastereoselective acylation and chemoselective reduction-lactonization
The syntheses of methylenolactocin, nephrosterinic acid and their derivatives can be achieved by using the efficient diastereoselective acylation of dimethyl itaconate-anthracene adduct followed by tandem chemoselective reduction-lactonization. © 2009 Elsevier Ltd. All rights reserved.
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| Main Authors: | , , , , |
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| Format: | Journal |
| Published: |
2018
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| Subjects: | |
| Online Access: | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=67649840195&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/48859 |
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| Institution: | Chiang Mai University |
| Summary: | The syntheses of methylenolactocin, nephrosterinic acid and their derivatives can be achieved by using the efficient diastereoselective acylation of dimethyl itaconate-anthracene adduct followed by tandem chemoselective reduction-lactonization. © 2009 Elsevier Ltd. All rights reserved. |
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