Journal
CHEMISTRY LETTERS
Volume 42, Issue 8, Pages 904-905Publisher
CHEMICAL SOC JAPAN
DOI: 10.1246/cl.130304
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Funding
- MEXT [25708018]
- ACT-C from JST
- Asahi Glass Foundation
- JSPS
- [21245028]
- [23105546]
- 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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