Nitrogen-Philic Cyclization of Acyl Radicals Enables the Synthesis of Lactams

Takahide Fukuyama, Ilhyong Ryu*

*Corresponding author for this work

    Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

    1 Scopus citations

    Abstract

    This chapter focuses on the synthesis of lactams that is enabled by the high affinity of acyl radicals for the N–C double bond in compounds such as imines, amines, oxazolines, and azides. Such acyl radicals can be generated as the first intermediates via the radical carbonylation with carbon monoxide.

    Original languageEnglish
    Title of host publicationProgress in Heterocyclic Chemistry
    PublisherElsevier Ltd
    Pages1-12
    Number of pages12
    DOIs
    StatePublished - 1 Jan 2018

    Publication series

    NameProgress in Heterocyclic Chemistry
    Volume30
    ISSN (Print)0959-6380

    Keywords

    • acyl radicals
    • amidine
    • amine
    • azide
    • carbon monoxide
    • imine
    • lactams
    • nitrogen-philic cyclization
    • radical carbonylation

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