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: | Rattana Jongkol, Ruangrat Choommongkol, Bongkoch Tarnchompoo, Piyarat Nimmanpipug, Puttinan Meepowpan |
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格式: | 雜誌 |
出版: |
2018
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在線閱讀: | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=67649840195&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/59353 |
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機構: | Chiang Mai University |
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