封面：伊奈苷 A 的首次全合成（《亚洲有机化学杂志》12/2024 期）

IF 2.8 4区化学 Q1 CHEMISTRY, ORGANIC

Asian Journal of Organic Chemistry Pub Date : 2024-12-13 DOI:10.1002/ajoc.202481201

Tomoya Takao, Atsushi Kawamura, Hidefumi Makabe

{"title":"封面：伊奈苷 A 的首次全合成（《亚洲有机化学杂志》12/2024 期）","authors":"Tomoya Takao, Atsushi Kawamura, Hidefumi Makabe","doi":"10.1002/ajoc.202481201","DOIUrl":null,"url":null,"abstract":"<p>In article number e202400547, Tomoya Takao, Atsushi Kawamura, and Hidefumi Makabe accomplished the first total synthesis of inaoside A, isolated from the edible mushroom <i>Laetiporus cremeiporus</i>, using α-selective Schmidt glycosylation of the easily prepared 2,3,5-tri-TBS-protected ribofuranosyl trichloroacetimidate as a key step. In this cover picture, the creatures of <i>L. cremeiours</i> are trying to build inaoside by guiding the aglycon to the α-face of the ribose derivative.\n <figure>\n <div><picture>\n <source></source></picture><p></p>\n </div>\n </figure>\n </p>","PeriodicalId":130,"journal":{"name":"Asian Journal of Organic Chemistry","volume":"13 12","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2024-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ajoc.202481201","citationCount":"0","resultStr":"{\"title\":\"Front Cover: First Total Synthesis of Inaoside A (Asian J. Org. Chem. 12/2024)\",\"authors\":\"Tomoya Takao, Atsushi Kawamura, Hidefumi Makabe\",\"doi\":\"10.1002/ajoc.202481201\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>In article number e202400547, Tomoya Takao, Atsushi Kawamura, and Hidefumi Makabe accomplished the first total synthesis of inaoside A, isolated from the edible mushroom <i>Laetiporus cremeiporus</i>, using α-selective Schmidt glycosylation of the easily prepared 2,3,5-tri-TBS-protected ribofuranosyl trichloroacetimidate as a key step. In this cover picture, the creatures of <i>L. cremeiours</i> are trying to build inaoside by guiding the aglycon to the α-face of the ribose derivative.\\n <figure>\\n <div><picture>\\n <source></source></picture><p></p>\\n </div>\\n </figure>\\n </p>\",\"PeriodicalId\":130,\"journal\":{\"name\":\"Asian Journal of Organic Chemistry\",\"volume\":\"13 12\",\"pages\":\"\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2024-12-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ajoc.202481201\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Asian Journal of Organic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/ajoc.202481201\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Asian Journal of Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/ajoc.202481201","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}

引用次数: 0

摘要

在文章编号e202400547中，Tomoya Takao、Atsushi Kawamura和Hidefumi Makabe首次完成了从食用菌Laetiporus cremeiporus中分离得到的稻皂苷A的全合成，并将易于制备的2,3,5-tri- tbs保护的三氯乙酰咪酯核氟烷基α-选择性施密特糖基化作为关键步骤。在这张封面图片中，L. cremeiours的生物正试图通过将糖基引导到核糖衍生物的α-面来构建苷。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

Front Cover: First Total Synthesis of Inaoside A (Asian J. Org. Chem. 12/2024)

查看原文本刊更多论文

Front Cover: First Total Synthesis of Inaoside A (Asian J. Org. Chem. 12/2024)

In article number e202400547, Tomoya Takao, Atsushi Kawamura, and Hidefumi Makabe accomplished the first total synthesis of inaoside A, isolated from the edible mushroom Laetiporus cremeiporus, using α-selective Schmidt glycosylation of the easily prepared 2,3,5-tri-TBS-protected ribofuranosyl trichloroacetimidate as a key step. In this cover picture, the creatures of L. cremeiours are trying to build inaoside by guiding the aglycon to the α-face of the ribose derivative.

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

Asian Journal of Organic Chemistry CHEMISTRY, ORGANIC-

CiteScore

4.70

自引率

3.70%

发文量

372

期刊介绍： Organic chemistry is the fundamental science that stands at the heart of chemistry, biology, and materials science. Research in these areas is vigorous and truly international, with three major regions making almost equal contributions: America, Europe and Asia. Asia now has its own top international organic chemistry journal—the Asian Journal of Organic Chemistry (AsianJOC) The AsianJOC is designed to be a top-ranked international research journal and publishes primary research as well as critical secondary information from authors across the world. The journal covers organic chemistry in its entirety. Authors and readers come from academia, the chemical industry, and government laboratories.