Bitter Principles ofAilanthus altissimaSWINGLE. Conversion of Ailanthone into Shinjulactone C
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/58/8/58_8_2357/_pdf
Reference10 articles.
1. Conversion of ailanthone into shinjulactone C through an ionic [4+2] cycloaddition reaction
2. Constituents of the Root Bark ofAilanthus altissimaSWINGLE. Isolation and X-Ray Crystal Structures of Shinjudilactone and Shinjulactone C and Conversion of Ailanthone into Shinjudilactone
3. Structure Determination of Bitter Principles ofAilanthus altissima. Structures of Shinjulactones B, D, and E
4. Structure Determination of Bitter Principles inAilanthus altissima.Structure of Shinjulactone A and Revised Structure of Ailanthone
5. Conversion of ailanthone into shinjudilactone, a backbone-rearranged picrasane.
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1. Fingerprint analysis and pharmacological evaluation of Ailanthus altissima;International Journal of Molecular Medicine;2018-02-14
2. Antitumor Activities of Six Quassinoids from Ailanthus altissima;Chemistry of Natural Compounds;2017-01
3. Development of a validated LC–MS/MS method for the determination of ailanthone in rat plasma with application to pharmacokinetic study;Journal of Pharmaceutical and Biomedical Analysis;2015-01
4. Shinjulactone O, a new quassinoid from the root bark ofAilanthus altissima;Natural Product Research;2014-06-26
5. [5 + 2] Cycloaddition Reactions in Organic and Natural Product Synthesis;Chemical Reviews;2012-11-15
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