Journal
ORGANIC LETTERS
Volume 13, Issue 7, Pages 1698-1701Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol2002094
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Funding
- Ministry of Education, Culture, Sports, Science, and Technology of Japan [22105006, 21245024, 20200049]
- Grants-in-Aid for Scientific Research [22105006, 20200049, 21245024] Funding Source: KAKEN
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An efficient one-to-one coupling reaction of atmospheric pressure carbon dioxide with 1,3-dienes is realized for the first time through PSiP-pincer type palladium-catalyzed hydrocarboxylation. The reaction is applicable to various 1,3-dienes including easily available chemical feedstock such as 1,3-butadiene and Isoprene. This protocol affords a highly useful method for the synthesis of beta,gamma-unsaturated carboxylic acid derivatives from CO(2).
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