4.7 Article

Gold(I)-Catalyzed Regioselective Inter-/Intramolecular Addition Cascade of Di- and Triynes for Direct Construction of Substituted Naphthalenes

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 77, Issue 11, Pages 4907-4916

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jo300771f

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Funding

  1. Ministry of Education, Culture, Sports, Science and Technology of Japan
  2. JSPS for Young Scientists
  3. Grants-in-Aid for Scientific Research [24106720, 24689001] Funding Source: KAKEN

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The gold-catalyzed cascade intermolecular addition-intramolecular carbocyclization reaction of diallcynylbenzenes was developed. In this reaction, regioselective addition of an external nucleophile toward the terminal alkyne and subsequent 6-endo-dig cyclization proceeded to give the 1,3-disubstituted naphthalenes in good yields. The direct synthesis of disubstituted chrysenes via a gold-catalyzed addition and double cyclization cascade using a triyne-type substrate was also achieved.

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