Literature DB >> 30707588

Electrochemical Radical Selenylation/1,2-Carbon Migration and Dowd-Beckwith-Type Ring-Expansion Sequences of Alkenylcyclobutanols.

Yeon Joo Kim1, Dae Young Kim1.   

Abstract

Electrochemical oxidative radical selenylation/1,2-carbon migration and Dowd-Beckwith-type ring-expansion sequences of alkenylcyclobutanols were developed in this study. This approach is environmentally benign and uses shelf-stable diselenides as selenium radical precursors and electrons as oxidizing reagents. The present protocol offers a facile way to prepare β-selenated cyclic ketone derivatives. Under Dowd-Beckwith-type rearrangement, it can afford the corresponding one-carbon ring-expanded ketones.

Entities:  

Year:  2019        PMID: 30707588     DOI: 10.1021/acs.orglett.8b04041

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

Review 1.  Recent Advances in the Synthesis of Selenophenes and Their Derivatives.

Authors:  Paola S Hellwig; Thiago J Peglow; Filipe Penteado; Luana Bagnoli; Gelson Perin; Eder J Lenardão
Journal:  Molecules       Date:  2020-12-13       Impact factor: 4.411

2.  Iron-Catalyzed Photoinduced LMCT: a 1° C-H Abstraction Enables Skeletal Rearrangements and C(sp3)-H Alkylation.

Authors:  Yi Cheng Kang; Sean M Treacy; Tomislav Rovis
Journal:  ACS Catal       Date:  2021-06-08       Impact factor: 13.700

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.