Regiospecific Synthesis of 5- and 6-Acylated Naphtho[1,2- b ]benzofurans via Intramolecular Alkyne Carbonyl Metathesis

Maloy Nayak, Dileep Kumar Singh, Ikyon Kim

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

Straightforward access to various 5- and 6-acylated naphtho[1,2-b]benzofurans was achieved by successive Sonogashira coupling and intramolecular alkyne carbonyl metathesis to assemble the central aromatic C ring of naphtho[1,2-b]benzofurans regiospecifically substituted with an acyl group at the C5 or C6 position.

Original languageEnglish
Article numberss-2016-f0747-op
Pages (from-to)2063-2073
Number of pages11
JournalSynthesis (Germany)
Volume49
Issue number9
DOIs
Publication statusPublished - 2017 May 3

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Benzofurans
Alkynes

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Organic Chemistry

Cite this

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Regiospecific Synthesis of 5- and 6-Acylated Naphtho[1,2- b ]benzofurans via Intramolecular Alkyne Carbonyl Metathesis. / Nayak, Maloy; Singh, Dileep Kumar; Kim, Ikyon.

In: Synthesis (Germany), Vol. 49, No. 9, ss-2016-f0747-op, 03.05.2017, p. 2063-2073.

Research output: Contribution to journalArticle

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