Literature DB >> 30256503

Intermolecular Allylic C-H Etherification of Internal Olefins.

Taylor A F Nelson1, Simon B Blakey1.   

Abstract

Herein we report on the development of an oxidative allylic C-H etherification reaction, utilizing internal olefins and alcohols as simple precursors. Key advances include the use of RhCp* complexes to promote the allylic C-H functionalization of internal olefins and the compatibility of the oxidative conditions with oxidatively sensitive alcohols, enabling the direct etherification reaction. Preliminary mechanistic studies, consistent with C-H functionalization as the rate determining step, are presented.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  C−H functionalization; etherification; intermolecular reactions; rhodium; π-allyl

Year:  2018        PMID: 30256503     DOI: 10.1002/anie.201809863

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  2 in total

1.  Computational insights into Ir(iii)-catalyzed allylic C-H amination of terminal alkenes: mechanism, regioselectivity, and catalytic activity.

Authors:  Deng Pan; Gen Luo; Yang Yu; Jimin Yang; Yi Luo
Journal:  RSC Adv       Date:  2021-05-26       Impact factor: 4.036

2.  Site-Selective Alkoxylation of Benzylic C-H Bonds by Photoredox Catalysis.

Authors:  Byung Joo Lee; Kimberly S DeGlopper; Tehshik P Yoon
Journal:  Angew Chem Int Ed Engl       Date:  2019-11-18       Impact factor: 15.336

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.