Journal
ORGANIC LETTERS
Volume 12, Issue 15, Pages 3390-3393Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol1012108
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Funding
- Ministry of Education, Culture, Sports, Science and Technology, Japan [18065015, 20036036, 19550038]
- Grants-in-Aid for Scientific Research [19550038, 18065015, 20036036] Funding Source: KAKEN
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The regioselective carboindation of simple alkenes with indium tribromide and ketene silyl acetals was accomplished. Various alkenes such as ethylene, 1-alkenes, and cyclic alkenes were applicable for this reaction system. The alkylindium product from the carboindation of cyclohexene revealed an anti addition mechanism.
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