Journal
ORGANIC LETTERS
Volume 16, Issue 14, Pages 3828-3831Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol501744g
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Funding
- MEXT, Japan [26248030]
- MEXT
- Grants-in-Aid for Scientific Research [26870389, 26248030] Funding Source: KAKEN
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Use of a bismuth catalyst allowed efficient dehydrative substitution of phenolic hydroxy groups with alcohols and thiols to form C-O and C-S bonds. The reaction required equimolar amounts of two readily available substrates that generated H2O as the only byproduct. The relatively mild reaction conditions were compatible with the functional groups selected, and provided excellent chemoselectivity.
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