紫杉醇C环的对映选择性合成

Collection of Czechoslovak Chemical Communications Pub Date : 2011-12-23 DOI:10.1135/CCCC2011039

Cong Ma, Stéphanie Schiltz, Joëlle Prunet

{"title":"紫杉醇C环的对映选择性合成","authors":"Cong Ma, Stéphanie Schiltz, Joëlle Prunet","doi":"10.1135/CCCC2011039","DOIUrl":null,"url":null,"abstract":"An enantioselective synthesis of a C ring of taxol has been accomplished. The key step is an oxidative cleavage of a derivative of the Wieland-Miescher ketone. A first attempt of a Shapiro reaction modelling the coupling of the C ring with the A fragment of taxol was also successful. © 2011 Institute of Organic Chemistry and Biochemistry.","PeriodicalId":10674,"journal":{"name":"Collection of Czechoslovak Chemical Communications","volume":"76 1","pages":"1579-1594"},"PeriodicalIF":0.0000,"publicationDate":"2011-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1135/CCCC2011039","citationCount":"5","resultStr":"{\"title\":\"Enantioselective synthesis of a taxol C ring\",\"authors\":\"Cong Ma, Stéphanie Schiltz, Joëlle Prunet\",\"doi\":\"10.1135/CCCC2011039\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"An enantioselective synthesis of a C ring of taxol has been accomplished. The key step is an oxidative cleavage of a derivative of the Wieland-Miescher ketone. A first attempt of a Shapiro reaction modelling the coupling of the C ring with the A fragment of taxol was also successful. © 2011 Institute of Organic Chemistry and Biochemistry.\",\"PeriodicalId\":10674,\"journal\":{\"name\":\"Collection of Czechoslovak Chemical Communications\",\"volume\":\"76 1\",\"pages\":\"1579-1594\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2011-12-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1135/CCCC2011039\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Collection of Czechoslovak Chemical Communications\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1135/CCCC2011039\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Collection of Czechoslovak Chemical Communications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1135/CCCC2011039","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}

引用次数: 5

摘要

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

微信好友朋友圈 QQ好友复制链接

本刊更多论文

Enantioselective synthesis of a taxol C ring

An enantioselective synthesis of a C ring of taxol has been accomplished. The key step is an oxidative cleavage of a derivative of the Wieland-Miescher ketone. A first attempt of a Shapiro reaction modelling the coupling of the C ring with the A fragment of taxol was also successful. © 2011 Institute of Organic Chemistry and Biochemistry.

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

Collection of Czechoslovak Chemical Communications 化学-化学综合

自引率

0.00%

发文量

审稿时长

6 months