Synthesis and structural affirmation of pubesamides A and B, monoterpene N-benzoyltyramides from white sapote (Casimiroa pubescens)

Ruth P. Paulino , Karen Ichikawa , Jonathan Sperry
{"title":"Synthesis and structural affirmation of pubesamides A and B, monoterpene N-benzoyltyramides from white sapote (Casimiroa pubescens)","authors":"Ruth P. Paulino ,&nbsp;Karen Ichikawa ,&nbsp;Jonathan Sperry","doi":"10.1016/j.tchem.2024.100075","DOIUrl":null,"url":null,"abstract":"<div><p>Pubesamides A and B are structurally unusual monoterpene <em>N</em>-benzoyltyramides isolated from <em>Casimiroa pubescens</em>, a tropical fruiting tree with known psychotropic properties. Herein we report the structural affirmation of both natural products through a chemical synthesis that features a Lewis-acid assisted cross-metathesis reaction between a 1,1-disubstituted alkene and a dienone in the presence of the Hoveyda-Grubbs second generation catalyst. Stereochemically pure samples of pubesamide A and B isomerise upon standing, suggesting they are both genuine natural products.</p></div>","PeriodicalId":74918,"journal":{"name":"Tetrahedron chem","volume":"10 ","pages":"Article 100075"},"PeriodicalIF":0.0000,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2666951X24000147/pdfft?md5=3c997764006db3c7f4cccf37b4f7f12d&pid=1-s2.0-S2666951X24000147-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tetrahedron chem","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666951X24000147","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Pubesamides A and B are structurally unusual monoterpene N-benzoyltyramides isolated from Casimiroa pubescens, a tropical fruiting tree with known psychotropic properties. Herein we report the structural affirmation of both natural products through a chemical synthesis that features a Lewis-acid assisted cross-metathesis reaction between a 1,1-disubstituted alkene and a dienone in the presence of the Hoveyda-Grubbs second generation catalyst. Stereochemically pure samples of pubesamide A and B isomerise upon standing, suggesting they are both genuine natural products.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
白刺桐(Casimiroa pubescens)单萜烯 N-苯甲酰基酰胺 A 和 B 的合成与结构鉴定
阴毛酰胺 A 和 B 是一种结构不寻常的单萜烯 N-苯甲酰基酰胺,它们是从一种具有已知精神药物特性的热带果树 Casimiroa pubescens 中分离出来的。在此,我们报告了通过化学合成确认这两种天然产物结构的方法,该方法的特点是在 Hoveyda-Grubbs 第二代催化剂存在下,1,1-二取代烯和二烯酮之间发生路易斯酸辅助的交叉甲基化反应。立体化学纯度较高的短叶酰胺 A 和 B 样品在静置后会发生异构化,这表明它们都是真正的天然产物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Tetrahedron chem
Tetrahedron chem Organic Chemistry
CiteScore
3.60
自引率
0.00%
发文量
0
审稿时长
27 days
期刊最新文献
Metal-free sulfenylation of pyrrolo[1,2-a]quinoxaline with diaryl disulfide facilitated by TBATB Synthesis of novel benzo fused bridged azaheterocycles through the reaction of chalcone with hydrazone Synthesis of novel fluorescent 3-pyrrolyl BODIPYs and their derivatives Supramolecular light-harvesting systems based on cyanostilbene derivatives Synthesis of Acylbenzo[b]thiophenes, benzofurans and indoles via intramolecular oxidative cyclization enabled by photocatalytic hydrogen atom transfer (HAT)
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1