Jing Wu , Xinman Guo , Jinghan Zou , Ziyu Wang , Weixing Chang , Lingyan Liu , Jing Li
{"title":"镍催化的高区域选择性烯基碳硼化双功能化:获得α-取代-γ-boro-δ-enoates。","authors":"Jing Wu , Xinman Guo , Jinghan Zou , Ziyu Wang , Weixing Chang , Lingyan Liu , Jing Li","doi":"10.1039/d5ob00364d","DOIUrl":null,"url":null,"abstract":"<div><div>A Ni-catalyzed highly regioselective carboborylation bifunctionalization of allenes was developed, and a series of α-substituted-γ-boro-δ-enoates were generated in good to high yields. This reaction has the advantages of mild reaction conditions, a wide substrate scope and good late-stage modification applications, providing a new strategy for the synthesis of configurationally defined trisubstituted vinyl boron compounds.</div></div>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":"23 16","pages":"Pages 3894-3898"},"PeriodicalIF":2.7000,"publicationDate":"2024-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ni-catalyzed highly regioselective carboborylation bifunctionalization of allenes: access to α-substituted-γ-boro-δ-enoates†\",\"authors\":\"Jing Wu , Xinman Guo , Jinghan Zou , Ziyu Wang , Weixing Chang , Lingyan Liu , Jing Li\",\"doi\":\"10.1039/d5ob00364d\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A Ni-catalyzed highly regioselective carboborylation bifunctionalization of allenes was developed, and a series of α-substituted-γ-boro-δ-enoates were generated in good to high yields. This reaction has the advantages of mild reaction conditions, a wide substrate scope and good late-stage modification applications, providing a new strategy for the synthesis of configurationally defined trisubstituted vinyl boron compounds.</div></div>\",\"PeriodicalId\":96,\"journal\":{\"name\":\"Organic & Biomolecular Chemistry\",\"volume\":\"23 16\",\"pages\":\"Pages 3894-3898\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2024-11-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic & Biomolecular Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1477052025002149\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/3/19 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic & Biomolecular Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1477052025002149","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/19 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Ni-catalyzed highly regioselective carboborylation bifunctionalization of allenes: access to α-substituted-γ-boro-δ-enoates†
A Ni-catalyzed highly regioselective carboborylation bifunctionalization of allenes was developed, and a series of α-substituted-γ-boro-δ-enoates were generated in good to high yields. This reaction has the advantages of mild reaction conditions, a wide substrate scope and good late-stage modification applications, providing a new strategy for the synthesis of configurationally defined trisubstituted vinyl boron compounds.
期刊介绍:
Organic & Biomolecular Chemistry is an international journal using integrated research in chemistry-organic chemistry. Founded in 2003 by the Royal Society of Chemistry, the journal is published in Semimonthly issues and has been indexed by SCIE, a leading international database. The journal focuses on the key research and cutting-edge progress in the field of chemistry-organic chemistry, publishes and reports the research results in this field in a timely manner, and is committed to becoming a window and platform for rapid academic exchanges among peers in this field. The journal's impact factor in 2023 is 2.9, and its CiteScore is 5.5.