T. Hatsui, 初井 敏英, T. Hashiguchi, 橋口 知一, H. Takeshita, 竹下 齊, トシヒデ ハツイ, トモカズ ハシグチ, ヒトシ タケシタ
{"title":"2,4-二氧戊酸甲酯与氯丁烯的光加成反应","authors":"T. Hatsui, 初井 敏英, T. Hashiguchi, 橋口 知一, H. Takeshita, 竹下 齊, トシヒデ ハツイ, トモカズ ハシグチ, ヒトシ タケシタ","doi":"10.15017/7869","DOIUrl":null,"url":null,"abstract":"The photoaddition reaction ofmethyl 2,4-dioxopentanoate with chloroprene gave two deMayo type adducts, methyl 3-(I-chlorovinyl)-2,6-dioxoheptanoate and methyl 3-chloro-2,6-dioxo-3-vinyl heptanoate. No regio isomers, 4-substituted esters, were observed. The photoadducts were converted to cyclohexenones and the selectivity of photoaddition was discussed.","PeriodicalId":22886,"journal":{"name":"The reports of Institute of Advanced Material Study Kyushu University","volume":"11 1","pages":"83-85"},"PeriodicalIF":0.0000,"publicationDate":"1997-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Photoaddition Reaction of Methyl 2,4-Dioxopentanoate with Chloroprene\",\"authors\":\"T. Hatsui, 初井 敏英, T. Hashiguchi, 橋口 知一, H. Takeshita, 竹下 齊, トシヒデ ハツイ, トモカズ ハシグチ, ヒトシ タケシタ\",\"doi\":\"10.15017/7869\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The photoaddition reaction ofmethyl 2,4-dioxopentanoate with chloroprene gave two deMayo type adducts, methyl 3-(I-chlorovinyl)-2,6-dioxoheptanoate and methyl 3-chloro-2,6-dioxo-3-vinyl heptanoate. No regio isomers, 4-substituted esters, were observed. The photoadducts were converted to cyclohexenones and the selectivity of photoaddition was discussed.\",\"PeriodicalId\":22886,\"journal\":{\"name\":\"The reports of Institute of Advanced Material Study Kyushu University\",\"volume\":\"11 1\",\"pages\":\"83-85\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1997-12-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The reports of Institute of Advanced Material Study Kyushu University\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.15017/7869\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The reports of Institute of Advanced Material Study Kyushu University","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15017/7869","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Photoaddition Reaction of Methyl 2,4-Dioxopentanoate with Chloroprene
The photoaddition reaction ofmethyl 2,4-dioxopentanoate with chloroprene gave two deMayo type adducts, methyl 3-(I-chlorovinyl)-2,6-dioxoheptanoate and methyl 3-chloro-2,6-dioxo-3-vinyl heptanoate. No regio isomers, 4-substituted esters, were observed. The photoadducts were converted to cyclohexenones and the selectivity of photoaddition was discussed.