4.3 Article

Nickel-catalyzed [2+2] Cycloaddition Reaction of Bulky Enones with Simple Alkynes. The Effect of Bulkiness of Substituent Attached at β-Carbon

Journal

CHEMISTRY LETTERS
Volume 42, Issue 8, Pages 904-905

Publisher

CHEMICAL SOC JAPAN
DOI: 10.1246/cl.130304

Keywords

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Funding

  1. MEXT [25708018]
  2. ACT-C from JST
  3. Asahi Glass Foundation
  4. JSPS
  5. [21245028]
  6. [23105546]
  7. Grants-in-Aid for Scientific Research [21245028, 25105736, 25708018] Funding Source: KAKEN

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In the presence of a catalytic amount of [Ni(cod)(2)] and PCy3, the [2 + 2] cycloaddition of enones bearing a bulky substituent group at the beta-position with simple alkynes occurs to give cyclobutenes. The bulky group at the beta-position can suppress the insertion of either an enone to give a cyclohexene or an allcyne to give a cyclohexadiene.

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