{"title":"铂催化的 1,8-二氨基萘保护二硼酸（B2(dan)2）对炔烃的二化反应","authors":"Shinichi Saito*, Yuya Koizumi, Yuki Ito, Taiga Yasuda and Yusuke Yoshigoe, ","doi":"10.1021/acs.joc.4c0193910.1021/acs.joc.4c01939","DOIUrl":null,"url":null,"abstract":"<p >The diboration of alkynes by 1,8-diaminonaphthalene-protected diboronic acid (B<sub>2</sub>(dan)<sub>2</sub>) proceeded smoothly in the presence of a platinum catalyst, and 1,2-diborylalkenes were isolated in up to 94% yield. The use of an appropriate solvent and ligand was critical for the progress of the reaction. The derivatization of 1,2-diborylalkenes was briefly examined.</p>","PeriodicalId":57,"journal":{"name":"The Journal of Organic Chemistry","volume":"89 22","pages":"16947–16951 16947–16951"},"PeriodicalIF":3.3000,"publicationDate":"2024-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/epdf/10.1021/acs.joc.4c01939","citationCount":"0","resultStr":"{\"title\":\"Platinum-Catalyzed Diboration of Alkynes by 1,8-Diaminonaphthalene-Protected Diboronic Acid (B2(dan)2)\",\"authors\":\"Shinichi Saito*, Yuya Koizumi, Yuki Ito, Taiga Yasuda and Yusuke Yoshigoe, \",\"doi\":\"10.1021/acs.joc.4c0193910.1021/acs.joc.4c01939\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The diboration of alkynes by 1,8-diaminonaphthalene-protected diboronic acid (B<sub>2</sub>(dan)<sub>2</sub>) proceeded smoothly in the presence of a platinum catalyst, and 1,2-diborylalkenes were isolated in up to 94% yield. The use of an appropriate solvent and ligand was critical for the progress of the reaction. The derivatization of 1,2-diborylalkenes was briefly examined.</p>\",\"PeriodicalId\":57,\"journal\":{\"name\":\"The Journal of Organic Chemistry\",\"volume\":\"89 22\",\"pages\":\"16947–16951 16947–16951\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2024-10-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.acs.org/doi/epdf/10.1021/acs.joc.4c01939\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Journal of Organic Chemistry\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.joc.4c01939\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Organic Chemistry","FirstCategoryId":"1","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.joc.4c01939","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Platinum-Catalyzed Diboration of Alkynes by 1,8-Diaminonaphthalene-Protected Diboronic Acid (B2(dan)2)
The diboration of alkynes by 1,8-diaminonaphthalene-protected diboronic acid (B2(dan)2) proceeded smoothly in the presence of a platinum catalyst, and 1,2-diborylalkenes were isolated in up to 94% yield. The use of an appropriate solvent and ligand was critical for the progress of the reaction. The derivatization of 1,2-diborylalkenes was briefly examined.
期刊介绍：
The Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.
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