生物启发Schenck-ene/Hock/Aldol级联反应使天然产物Alstoscholarinoid A， Masterpenoid D， Leontogenin和marsformo氧化物B的合成简洁

IF 9.2 1区化学 Q1 CHEMISTRY, MULTIDISCIPLINARY

CCS Chemistry Pub Date : 2025-09-08 DOI:10.31635/ccschem.025.202506037

Ruoxi Li, Tongkun Wang, Xiaosong Xue & Jingjing Wu1State Key Laboratory of Synergistic Chem-Bio Synthesis, Frontiers Science Center for Transformative Molecules, Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, School of Chemistry and Chemical Engineering, Zhangjiang Institute for Advanced Study, Shanghai Jiao Tong University, Shanghai 2002402State Key Laboratory of Fluorine and Nitrogen Chemistry and Advanced Materials, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai 200032

{"title":"生物启发Schenck-ene/Hock/Aldol级联反应使天然产物Alstoscholarinoid A， Masterpenoid D， Leontogenin和marsformo氧化物B的合成简洁","authors":"Ruoxi Li, Tongkun Wang, Xiaosong Xue & Jingjing Wu1State Key Laboratory of Synergistic Chem-Bio Synthesis, Frontiers Science Center for Transformative Molecules, Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, School of Chemistry and Chemical Engineering, Zhangjiang Institute for Advanced Study, Shanghai Jiao Tong University, Shanghai 2002402State Key Laboratory of Fluorine and Nitrogen Chemistry and Advanced Materials, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai 200032","doi":"10.31635/ccschem.025.202506037","DOIUrl":null,"url":null,"abstract":"CCS Chemistry, Ahead of Print.<br/>In the research discussed in this paper, we achieve the concise synthesis of four natural products—alstoscholarinoid A, masterpenoid D, leontogenin, and marsformoxide B—through a skeletal editing strategy. Our approach features a novel bioinspired Schenck-...","PeriodicalId":9810,"journal":{"name":"CCS Chemistry","volume":"15 1","pages":""},"PeriodicalIF":9.2000,"publicationDate":"2025-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bioinspired Schenck-ene/Hock/Aldol Cascade Reaction Enables Concise Synthesis of Natural Products Alstoscholarinoid A, Masterpenoid D, Leontogenin, and Marsformoxide B\",\"authors\":\"Ruoxi Li, Tongkun Wang, Xiaosong Xue & Jingjing Wu1State Key Laboratory of Synergistic Chem-Bio Synthesis, Frontiers Science Center for Transformative Molecules, Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, School of Chemistry and Chemical Engineering, Zhangjiang Institute for Advanced Study, Shanghai Jiao Tong University, Shanghai 2002402State Key Laboratory of Fluorine and Nitrogen Chemistry and Advanced Materials, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai 200032\",\"doi\":\"10.31635/ccschem.025.202506037\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"CCS Chemistry, Ahead of Print.<br/>In the research discussed in this paper, we achieve the concise synthesis of four natural products—alstoscholarinoid A, masterpenoid D, leontogenin, and marsformoxide B—through a skeletal editing strategy. Our approach features a novel bioinspired Schenck-...\",\"PeriodicalId\":9810,\"journal\":{\"name\":\"CCS Chemistry\",\"volume\":\"15 1\",\"pages\":\"\"},\"PeriodicalIF\":9.2000,\"publicationDate\":\"2025-09-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"CCS Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.31635/ccschem.025.202506037\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"CCS Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31635/ccschem.025.202506037","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}

引用次数: 0

摘要

CCS化学，领先于印刷。在本文所讨论的研究中，我们通过骨骼编辑策略实现了四种天然产物- alstoscholarinoid A， masterpenoid D， leontogenin和marsformmo氧化物b的简洁合成。我们的方法采用了一种新颖的生物灵感申克-…

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文本刊更多论文

Bioinspired Schenck-ene/Hock/Aldol Cascade Reaction Enables Concise Synthesis of Natural Products Alstoscholarinoid A, Masterpenoid D, Leontogenin, and Marsformoxide B

CCS Chemistry, Ahead of Print.
In the research discussed in this paper, we achieve the concise synthesis of four natural products—alstoscholarinoid A, masterpenoid D, leontogenin, and marsformoxide B—through a skeletal editing strategy. Our approach features a novel bioinspired Schenck-...

求助全文

通过发布文献求助，成功后即可免费获取论文全文。去求助

来源期刊

CCS Chemistry Chemistry-General Chemistry

CiteScore

13.60

自引率

13.40%

发文量

475

审稿时长

10 weeks

期刊介绍： CCS Chemistry, the flagship publication of the Chinese Chemical Society, stands as a leading international chemistry journal based in China. With a commitment to global outreach in both contributions and readership, the journal operates on a fully Open Access model, eliminating subscription fees for contributing authors. Issued monthly, all articles are published online promptly upon reaching final publishable form. Additionally, authors have the option to expedite the posting process through Immediate Online Accepted Article posting, making a PDF of their accepted article available online upon journal acceptance.