Journal
ORGANIC LETTERS
Volume 12, Issue 15, Pages 3450-3452Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol101264r
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Funding
- MEXT [21245028, 21750102]
- Nagase Science and Technology Foundation
- Japan Petroleum Institute
- Grants-in-Aid for Scientific Research [21750102] Funding Source: KAKEN
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A fully intermolecular [2 + 2 + 2] cycloaddition of two enones and an alkyne has been achieved. This reaction proceeds stereoselectively to give one diastereomer as a sole product.
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