Journal
CHEMICAL COMMUNICATIONS
Volume 53, Issue 26, Pages 3753-3756Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7cc01070b
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Funding
- Japan Society for the Promotion of Science [16J06159]
- [26288087]
- Grants-in-Aid for Scientific Research [16J06159, 26288087] Funding Source: KAKEN
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We established a highly enantioselective Si-H insertion reaction to construct chiral centers at the carbon and silicon atoms, using a Ru(II)-pheox catalyst. The catalytic asymmetric Si-H insertion reaction of alpha-methyl-alpha-diazoesters proceeded smoothly with excellent stereoinduction at both the neighboring carbon and silicon atoms (up to 99% yield and 99% ee).
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