{"title":"Functionalization of Lewis base (LB) in LB–BR3 adducts","authors":"Pan Xu , Xuenian Chen , Zhenxing Liu","doi":"10.1016/j.tetlet.2024.155372","DOIUrl":null,"url":null,"abstract":"<div><div>Whenever a Lewis base borane is formed, the Lewis base will affect the properties of borane. The opposite is similarly true, that borane will affect the properties of Lewis base. The current development of Lewis base borane adducts mainly focuses on the borane part. Less chemistry is known about the Lewis base part. Herein, we selected examples to highlight the functionalization of the Lewis base of LB–BR<sub>3</sub> adducts. Parts I and II focus on showing how boranes promote coupling, substitution, and reduction reactions of amine and phosphine in the corresponding borane adducts, as well as borane’s control of the regioselectivity and stereoselectivity of amine-boron and phosphine-borane analogs. Part III focuses on the effect of boranes on the chemistry of Lewis bases containing carbon, oxygen, and sulfur.</div></div>","PeriodicalId":438,"journal":{"name":"Tetrahedron Letters","volume":"154 ","pages":"Article 155372"},"PeriodicalIF":1.5000,"publicationDate":"2024-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tetrahedron Letters","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0040403924004672","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0
Abstract
Whenever a Lewis base borane is formed, the Lewis base will affect the properties of borane. The opposite is similarly true, that borane will affect the properties of Lewis base. The current development of Lewis base borane adducts mainly focuses on the borane part. Less chemistry is known about the Lewis base part. Herein, we selected examples to highlight the functionalization of the Lewis base of LB–BR3 adducts. Parts I and II focus on showing how boranes promote coupling, substitution, and reduction reactions of amine and phosphine in the corresponding borane adducts, as well as borane’s control of the regioselectivity and stereoselectivity of amine-boron and phosphine-borane analogs. Part III focuses on the effect of boranes on the chemistry of Lewis bases containing carbon, oxygen, and sulfur.
期刊介绍:
Tetrahedron Letters provides maximum dissemination of outstanding developments in organic chemistry. The journal is published weekly and covers developments in techniques, structures, methods and conclusions in experimental and theoretical organic chemistry. Rapid publication of timely and significant research results enables researchers from all over the world to transmit quickly their new contributions to large, international audiences.