一种用碘基苯生成氧化腈的简便方法及其反应。

Nippon Kagaku Kaishi Pub Date : 2002-01-01 DOI:10.1246/NIKKASHI.2002.471

Seiji Tanaka, Mikinao Ito, K. Kishikawa, S. Kohmoto, Makoto Yamamoto*

{"title":"一种用碘基苯生成氧化腈的简便方法及其反应。","authors":"Seiji Tanaka, Mikinao Ito, K. Kishikawa, S. Kohmoto, Makoto Yamamoto*","doi":"10.1246/NIKKASHI.2002.471","DOIUrl":null,"url":null,"abstract":"A mild and convenient method for generation of nitrile oxide is established by iodosylbenzene oxidation of aldehyde oximes. Aldehyde oximes were converted to furoxans in almost quantitative yields via dimerization of corresponding nitrile oxides upon oxidation. When the oxidation was carried out in the presence of alkene and alkyne dipolarophiles, isoxazolines or isoxazoles were obtained in good yields.","PeriodicalId":19311,"journal":{"name":"Nippon Kagaku Kaishi","volume":"25 7-8 1","pages":"471-473"},"PeriodicalIF":0.0000,"publicationDate":"2002-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"13","resultStr":"{\"title\":\"A Convenient Method of Generation of Nitrile Oxides by Iodosylbenzene and Its Reaction.\",\"authors\":\"Seiji Tanaka, Mikinao Ito, K. Kishikawa, S. Kohmoto, Makoto Yamamoto*\",\"doi\":\"10.1246/NIKKASHI.2002.471\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A mild and convenient method for generation of nitrile oxide is established by iodosylbenzene oxidation of aldehyde oximes. Aldehyde oximes were converted to furoxans in almost quantitative yields via dimerization of corresponding nitrile oxides upon oxidation. When the oxidation was carried out in the presence of alkene and alkyne dipolarophiles, isoxazolines or isoxazoles were obtained in good yields.\",\"PeriodicalId\":19311,\"journal\":{\"name\":\"Nippon Kagaku Kaishi\",\"volume\":\"25 7-8 1\",\"pages\":\"471-473\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2002-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"13\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nippon Kagaku Kaishi\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1246/NIKKASHI.2002.471\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nippon Kagaku Kaishi","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1246/NIKKASHI.2002.471","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}

引用次数: 13

摘要

建立了一种温和、简便的用碘基苯氧化醛肟生成氧化腈的方法。在氧化过程中，通过相应的腈氧化物二聚化反应，醛肟几乎定量地转化为呋喃嘧啶。在烯烃和炔双极亲和试剂的存在下进行氧化，得到收率较高的异恶唑或异恶唑。

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

A Convenient Method of Generation of Nitrile Oxides by Iodosylbenzene and Its Reaction.

A mild and convenient method for generation of nitrile oxide is established by iodosylbenzene oxidation of aldehyde oximes. Aldehyde oximes were converted to furoxans in almost quantitative yields via dimerization of corresponding nitrile oxides upon oxidation. When the oxidation was carried out in the presence of alkene and alkyne dipolarophiles, isoxazolines or isoxazoles were obtained in good yields.

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

Nippon Kagaku Kaishi

自引率

0.00%

发文量