These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Search MEDLINE/PubMed


  • Title: Nickel-Catalyzed Reductive Coupling of γ-Metalated Ketones with Unactivated Alkyl Bromides.
    Author: Cui N, Lin T, Wang YE, Wu J, Han Y, Xu X, Xue F, Xiong D, Walsh PJ, Mao J.
    Journal: Org Lett; 2022 Jun 10; 24(22):3987-3992. PubMed ID: 35639094.
    Abstract:
    A nickel-catalyzed reductive cross-coupling reaction of aryl cyclopropyl ketones with easily accessible unactivated alkyl bromides to access aryl alkyl ketones has been developed. This strategy facilitates access to various of γ-alkyl-substituted ketones via ring opening of cyclopropyl ketones (26 examples, 50-90% yield). Initial mechanistic studies revealed that the reaction proceeds via radical cleavage of the alkyl bromide.
    [Abstract] [Full Text] [Related] [New Search]