Shoko Suzuki, Hiroyuki Ito, M. Noike, S. Ishizuka, R. Nonaka, K. Funaki, T. Kodama, S. Sakaki, T. Nishino, Mina Ito, Toranosuke Takahasi, Y. Yokoyama*
{"title":"应用减压技术环境友好合成亚胺:低反应性胺的反应案例及计算化学研究","authors":"Shoko Suzuki, Hiroyuki Ito, M. Noike, S. Ishizuka, R. Nonaka, K. Funaki, T. Kodama, S. Sakaki, T. Nishino, Mina Ito, Toranosuke Takahasi, Y. Yokoyama*","doi":"10.4236/gsc.2020.101001","DOIUrl":null,"url":null,"abstract":"Recently, the development of environmentally friendly syntheses of imine \nderivatives, which were attracting great attention for their reactivity and \nstructure in various fields, progressed rapidly because the concept of green \nchemistry had deeply penetrated into society. In our previous work, we had reported \nnew synthetic methods of imine derivatives using some active amines under solvent- \nand catalyst-free reaction conditions. This synthetic reaction proceeded \nsmoothly and target compounds were obtained in excellent yields. In this system, \nwhen less reactive amines were used as substrates, the synthetic reaction was \nnot finished in the short reaction time, and the corresponding compounds were given \nin moderate yields. In order to solve this point, we tried to improve the \nreaction conditions of this method. Through this improvement, it was found that \npure target compounds could be obtained in excellent yields by using 1.1 \nequivalents of less reactive amines to aldehydes and extending the reaction \ntime compared with our previous work. In this paper, we will introduce the detail \nof this study, and also report the result of the investigation of the reaction \nproperty by computational chemistry.","PeriodicalId":12770,"journal":{"name":"Green and Sustainable Chemistry","volume":"50 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Environmentally Friendly Syntheses of Imines Applying the Pressure Reduction Technique: Reaction Cases of Less Reactive Amines and Studies by Computational Chemistry\",\"authors\":\"Shoko Suzuki, Hiroyuki Ito, M. Noike, S. Ishizuka, R. Nonaka, K. Funaki, T. Kodama, S. Sakaki, T. Nishino, Mina Ito, Toranosuke Takahasi, Y. Yokoyama*\",\"doi\":\"10.4236/gsc.2020.101001\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Recently, the development of environmentally friendly syntheses of imine \\nderivatives, which were attracting great attention for their reactivity and \\nstructure in various fields, progressed rapidly because the concept of green \\nchemistry had deeply penetrated into society. In our previous work, we had reported \\nnew synthetic methods of imine derivatives using some active amines under solvent- \\nand catalyst-free reaction conditions. This synthetic reaction proceeded \\nsmoothly and target compounds were obtained in excellent yields. In this system, \\nwhen less reactive amines were used as substrates, the synthetic reaction was \\nnot finished in the short reaction time, and the corresponding compounds were given \\nin moderate yields. In order to solve this point, we tried to improve the \\nreaction conditions of this method. Through this improvement, it was found that \\npure target compounds could be obtained in excellent yields by using 1.1 \\nequivalents of less reactive amines to aldehydes and extending the reaction \\ntime compared with our previous work. In this paper, we will introduce the detail \\nof this study, and also report the result of the investigation of the reaction \\nproperty by computational chemistry.\",\"PeriodicalId\":12770,\"journal\":{\"name\":\"Green and Sustainable Chemistry\",\"volume\":\"50 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-01-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Green and Sustainable Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4236/gsc.2020.101001\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Green and Sustainable Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4236/gsc.2020.101001","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Environmentally Friendly Syntheses of Imines Applying the Pressure Reduction Technique: Reaction Cases of Less Reactive Amines and Studies by Computational Chemistry
Recently, the development of environmentally friendly syntheses of imine
derivatives, which were attracting great attention for their reactivity and
structure in various fields, progressed rapidly because the concept of green
chemistry had deeply penetrated into society. In our previous work, we had reported
new synthetic methods of imine derivatives using some active amines under solvent-
and catalyst-free reaction conditions. This synthetic reaction proceeded
smoothly and target compounds were obtained in excellent yields. In this system,
when less reactive amines were used as substrates, the synthetic reaction was
not finished in the short reaction time, and the corresponding compounds were given
in moderate yields. In order to solve this point, we tried to improve the
reaction conditions of this method. Through this improvement, it was found that
pure target compounds could be obtained in excellent yields by using 1.1
equivalents of less reactive amines to aldehydes and extending the reaction
time compared with our previous work. In this paper, we will introduce the detail
of this study, and also report the result of the investigation of the reaction
property by computational chemistry.