Journal
ORGANOMETALLICS
Volume 31, Issue 9, Pages 3810-3813Publisher
AMER CHEMICAL SOC
DOI: 10.1021/om300286b
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Funding
- Funding Program for Next Generation World-Leading Researchers [GR025]
- Ministry of Education, Culture, Sports, Science and Technology, Japan
- JSPS
- Grants-in-Aid for Scientific Research [24105505] Funding Source: KAKEN
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Propargylic allylation of propargylic alcohols with alpha,beta-unsaturated aldehydes in the presence of a thiolate-bridged diruthenium complex and a secondary amine as cocatalysts has been found to give the corresponding propargylic allylated products, where the gamma-propargylation occurs selectively at the alpha,beta-unsaturated aldehydes, in high yields as a mixture of two diastereoisomers.
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