V. Zhdankin, A. Yoshimura, Kim Ngo, I. Mironova, Zachary S. Gardner, Nami Ogura, Akiharu Ueki, M. Yusubov, Akio Saito
{"title":"水溶液条件下从苯齐碘氧硼酸芳基酯生成苄炔及其与烷基芳基硫化物的反应","authors":"V. Zhdankin, A. Yoshimura, Kim Ngo, I. Mironova, Zachary S. Gardner, Nami Ogura, Akiharu Ueki, M. Yusubov, Akio Saito","doi":"10.24820/ark.5550190.p012.213","DOIUrl":null,"url":null,"abstract":"Mesityl benziodoxaborole triflate is a unique benzyne precursor under aqueous conditions in the presence of NaHCO 3 at room temperature. Reactions of alkyl aryl sulfides with benzyne generated under these conditions selectively afford the corresponding sulfonium salts. In contrast, the previously reported reactions of alkyl aryl sulfides with common benzyne precursors under strongly basic anhydrous conditions lead to various products of cyclization, rearrangement","PeriodicalId":8432,"journal":{"name":"Arkivoc","volume":null,"pages":null},"PeriodicalIF":0.8000,"publicationDate":"2024-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Generation of Benzyne from Aryl Benziodoxaborole Triflate under Aqueous Conditions and its Reactions with Alkyl Aryl Sulfides\",\"authors\":\"V. Zhdankin, A. Yoshimura, Kim Ngo, I. Mironova, Zachary S. Gardner, Nami Ogura, Akiharu Ueki, M. Yusubov, Akio Saito\",\"doi\":\"10.24820/ark.5550190.p012.213\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Mesityl benziodoxaborole triflate is a unique benzyne precursor under aqueous conditions in the presence of NaHCO 3 at room temperature. Reactions of alkyl aryl sulfides with benzyne generated under these conditions selectively afford the corresponding sulfonium salts. In contrast, the previously reported reactions of alkyl aryl sulfides with common benzyne precursors under strongly basic anhydrous conditions lead to various products of cyclization, rearrangement\",\"PeriodicalId\":8432,\"journal\":{\"name\":\"Arkivoc\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.8000,\"publicationDate\":\"2024-07-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Arkivoc\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.24820/ark.5550190.p012.213\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Arkivoc","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.24820/ark.5550190.p012.213","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Generation of Benzyne from Aryl Benziodoxaborole Triflate under Aqueous Conditions and its Reactions with Alkyl Aryl Sulfides
Mesityl benziodoxaborole triflate is a unique benzyne precursor under aqueous conditions in the presence of NaHCO 3 at room temperature. Reactions of alkyl aryl sulfides with benzyne generated under these conditions selectively afford the corresponding sulfonium salts. In contrast, the previously reported reactions of alkyl aryl sulfides with common benzyne precursors under strongly basic anhydrous conditions lead to various products of cyclization, rearrangement
期刊介绍:
Arkivoc publishes full papers (not accounts) describing sound original work that is of interest to organic chemists (in areas of synthetic organic chemistry, bio-organic, organometallic, theoretical, and physical organic chemistry:
General Papers describing sound original work
Reviews and Accounts of selected topics
Honorary Issues - Pay tribute to distinguished organic chemists (invited contributions)
Thematic Issues - Cover important current topics in organic chemistry
Regional Issues - Recognize organic chemistry in various countries.