Cationic Au(I)-catalyzed cycloisomerization of aromatic enynes for the synthesis of substituted naphthalenes

Takanori Shibata, Yasunori Ueno, Kazumasa Kanda

    Research output: Contribution to journalArticle

    76 Citations (Scopus)

    Abstract

    A cationic Au(I) complex catalyzed the cycloisomerization of aromatic enynes that possess a substituent on their alkyne terminus. Cyclization of the 6-endo-dig type proceeded dominantly to give 1,3-di- and 1,2,3-trisubstituted naphthalenes.

    Original languageEnglish
    Pages (from-to)411-414
    Number of pages4
    JournalSynlett
    Issue number3
    DOIs
    Publication statusPublished - 2006 Feb 15

    Fingerprint

    Naphthalenes
    Alkynes
    Cyclization

    Keywords

    • Catalysis
    • Cycloisomerization
    • Enynes
    • Gold
    • Indenes
    • Naphthalenes

    ASJC Scopus subject areas

    • Organic Chemistry

    Cite this

    Cationic Au(I)-catalyzed cycloisomerization of aromatic enynes for the synthesis of substituted naphthalenes. / Shibata, Takanori; Ueno, Yasunori; Kanda, Kazumasa.

    In: Synlett, No. 3, 15.02.2006, p. 411-414.

    Research output: Contribution to journalArticle

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