{"title":"一个","authors":"","doi":"10.7560/718494-004","DOIUrl":null,"url":null,"abstract":"-alkyl allenoate esters aromatic aldehydes to give 4 H -1,3-di-oxin-6-yl-propanoates 14 with excellent diastereoselectivity. Mech- anistic studies revealed that these complex heterocycles are obtained as a result of a four-step reaction cascade consisting of two consec-utive Morita–Baylis–Hillman reactions on the α - and γ -position, an acetalization, and a final ring-closing intramolecular oxa-Michael reaction.","PeriodicalId":336042,"journal":{"name":"Shooting Stars of the Small Screen","volume":"25 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2009-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A\",\"authors\":\"\",\"doi\":\"10.7560/718494-004\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"-alkyl allenoate esters aromatic aldehydes to give 4 H -1,3-di-oxin-6-yl-propanoates 14 with excellent diastereoselectivity. Mech- anistic studies revealed that these complex heterocycles are obtained as a result of a four-step reaction cascade consisting of two consec-utive Morita–Baylis–Hillman reactions on the α - and γ -position, an acetalization, and a final ring-closing intramolecular oxa-Michael reaction.\",\"PeriodicalId\":336042,\"journal\":{\"name\":\"Shooting Stars of the Small Screen\",\"volume\":\"25 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2009-12-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Shooting Stars of the Small Screen\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.7560/718494-004\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Shooting Stars of the Small Screen","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.7560/718494-004","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
芳香醛的-烷基烯丙酸酯得到4 H -1,3-二氧辛-6-基丙酸14,具有优异的非对映选择性。机理研究表明,这些复杂杂环是由α -和γ -位置上连续的Morita-Baylis-Hillman反应、缩化反应和最终的分子内oxa-Michael反应组成的四步反应级联反应的结果。
-alkyl allenoate esters aromatic aldehydes to give 4 H -1,3-di-oxin-6-yl-propanoates 14 with excellent diastereoselectivity. Mech- anistic studies revealed that these complex heterocycles are obtained as a result of a four-step reaction cascade consisting of two consec-utive Morita–Baylis–Hillman reactions on the α - and γ -position, an acetalization, and a final ring-closing intramolecular oxa-Michael reaction.