Journal
ORGANIC LETTERS
Volume 15, Issue 13, Pages 3258-3261Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol4012794
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Funding
- MEXT
- JSPS
- JST, Japan
- Grants-in-Aid for Scientific Research [25105733, 25288048] Funding Source: KAKEN
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A straightforward synthesis of phosphaisocoumarins is achieved by the rhodium-catalyzed oxidative coupling of diarylphosphinic and phenylphosphonic acid derivatives with alkynes. The P-OH groups effectively act as the key function for the regioselective C-H bond cleavage. Related oxidative coupling of phenylphosphine oxides with alkenes can also be conducted smoothly under similar conditions.
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