{"title":"缩合吡唑[3,4(4,3)-d]噻唑和吡唑[3,4(4,3)-d][1,4]噻嗪的合成新方法(微评)","authors":"Evgeniya S. Khodykina, Alexandra A. Kolodina","doi":"10.1007/s10593-023-03249-0","DOIUrl":null,"url":null,"abstract":"<p>\n<img alt=\"\" src=\"//media.springernature.com/lw172/springer-static/image/art%3A10.1007%2Fs10593-023-03249-0/MediaObjects/10593_2023_3249_Figc_HTML.png\" style=\"width:172px;max-width:none;\"/>\nThis microreview discusses the latest examples (2012–2022) of the synthesis of pyrazolo[3,4-<i>d</i>]-thiazoles, pyrazolo[4,3-<i>d</i>]thiazoles, pyrazolo[4,3-<i>b</i>][1,4]thiazines, and pyrazolo[3,4-<i>b</i>][1,4]-thiazines <i>via</i> two main approaches: annulation of the pyrazole ring to the thiazole or thiazine ring and, conversely, annulation of the thiazole or thiazine ring to the pyrazole ring.</p><figure></figure>","PeriodicalId":9770,"journal":{"name":"Chemistry of Heterocyclic Compounds","volume":null,"pages":null},"PeriodicalIF":1.4000,"publicationDate":"2023-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Recent methods for the synthesis of fused pyrazolo[3,4(4,3)-d]thiazoles and pyrazolo[3,4(4,3)-d][1,4]thiazines (microreview)\",\"authors\":\"Evgeniya S. Khodykina, Alexandra A. Kolodina\",\"doi\":\"10.1007/s10593-023-03249-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>\\n<img alt=\\\"\\\" src=\\\"//media.springernature.com/lw172/springer-static/image/art%3A10.1007%2Fs10593-023-03249-0/MediaObjects/10593_2023_3249_Figc_HTML.png\\\" style=\\\"width:172px;max-width:none;\\\"/>\\nThis microreview discusses the latest examples (2012–2022) of the synthesis of pyrazolo[3,4-<i>d</i>]-thiazoles, pyrazolo[4,3-<i>d</i>]thiazoles, pyrazolo[4,3-<i>b</i>][1,4]thiazines, and pyrazolo[3,4-<i>b</i>][1,4]-thiazines <i>via</i> two main approaches: annulation of the pyrazole ring to the thiazole or thiazine ring and, conversely, annulation of the thiazole or thiazine ring to the pyrazole ring.</p><figure></figure>\",\"PeriodicalId\":9770,\"journal\":{\"name\":\"Chemistry of Heterocyclic Compounds\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2023-11-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemistry of Heterocyclic Compounds\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1007/s10593-023-03249-0\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry of Heterocyclic Compounds","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1007/s10593-023-03249-0","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Recent methods for the synthesis of fused pyrazolo[3,4(4,3)-d]thiazoles and pyrazolo[3,4(4,3)-d][1,4]thiazines (microreview)
This microreview discusses the latest examples (2012–2022) of the synthesis of pyrazolo[3,4-d]-thiazoles, pyrazolo[4,3-d]thiazoles, pyrazolo[4,3-b][1,4]thiazines, and pyrazolo[3,4-b][1,4]-thiazines via two main approaches: annulation of the pyrazole ring to the thiazole or thiazine ring and, conversely, annulation of the thiazole or thiazine ring to the pyrazole ring.
期刊介绍:
The international journal Chemistry of Heterocyclic Compounds publishes original papers, short communications, reviews, and mini-reviews dealing with problems in the field of heterocyclic chemistry in Russian and English. The Journal also publishes reviews and annotations on new books and brief reports on conferences in the field of heterocyclic chemistry, as well as commemoratives dedicated to prominent heterocyclic chemists.