Yu. V. Myasoedova, G. N. Sakhabutdinova, E. R. Belyaeva, G. Z. Raskil’dina, G. Yu. Ishmuratov, S. S. Zlotsky
{"title":"苯乙二醛衍生物合成的新方法","authors":"Yu. V. Myasoedova, G. N. Sakhabutdinova, E. R. Belyaeva, G. Z. Raskil’dina, G. Yu. Ishmuratov, S. S. Zlotsky","doi":"10.1134/S0012500822600109","DOIUrl":null,"url":null,"abstract":"<p>The paper proposes a new one-pot ozonolytic synthesis of acylhydrazones from phenylacrolein acetals, which includes ozonolytic cleavage of the substrate in methanol and treatment of the intermediate peroxides with hydrazides of capric, nicotinic, isonicotinic, benzoic, and <i>para</i>-hydroxybenzoic acids taken in excess.</p>","PeriodicalId":530,"journal":{"name":"Doklady Chemistry","volume":"504 1","pages":"74 - 78"},"PeriodicalIF":0.8000,"publicationDate":"2022-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"New Method for the Synthesis of Phenylglyoxal Derivatives\",\"authors\":\"Yu. V. Myasoedova, G. N. Sakhabutdinova, E. R. Belyaeva, G. Z. Raskil’dina, G. Yu. Ishmuratov, S. S. Zlotsky\",\"doi\":\"10.1134/S0012500822600109\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The paper proposes a new one-pot ozonolytic synthesis of acylhydrazones from phenylacrolein acetals, which includes ozonolytic cleavage of the substrate in methanol and treatment of the intermediate peroxides with hydrazides of capric, nicotinic, isonicotinic, benzoic, and <i>para</i>-hydroxybenzoic acids taken in excess.</p>\",\"PeriodicalId\":530,\"journal\":{\"name\":\"Doklady Chemistry\",\"volume\":\"504 1\",\"pages\":\"74 - 78\"},\"PeriodicalIF\":0.8000,\"publicationDate\":\"2022-11-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Doklady Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1134/S0012500822600109\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Doklady Chemistry","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1134/S0012500822600109","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
New Method for the Synthesis of Phenylglyoxal Derivatives
The paper proposes a new one-pot ozonolytic synthesis of acylhydrazones from phenylacrolein acetals, which includes ozonolytic cleavage of the substrate in methanol and treatment of the intermediate peroxides with hydrazides of capric, nicotinic, isonicotinic, benzoic, and para-hydroxybenzoic acids taken in excess.
期刊介绍:
Doklady Chemistry is a journal that publishes new research in chemistry and chemical engineering of great significance. Initially the journal was a forum of the Russian Academy of Science and published only best contributions from Russia in the form of short articles. Now the journal welcomes submissions from any country in the English or Russian language. Every manuscript must be recommended by Russian or foreign members of the Russian Academy of Sciences.