期刊
ORGANIC LETTERS
卷 19, 期 14, 页码 3715-3718出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b01510
关键词
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资金
- KAKENHI from JSPS [26810056]
- JSPS [16F16749]
- JSPS
- NU through The World Premier International Research Center Initiative (WPI)
- Grants-in-Aid for Scientific Research [16K13962, 26288023, 17K17805, 26810056, 17H03030, 16F16749] Funding Source: KAKEN
The Pd-catalyzed desulfonative cross-coupling reaction of benzylic sulfone derivatives with 1,3-oxazoles via a deprotonative pathway has been developed. Broad substrate scope for both sulfone and 1,3-oxazole partners is observed, affording a variety of 1,3-oxazole-containing triarylmethanes. Sulfone partners that are primary benzylic, secondary benzylic, and benzhydryl are all effective. Using this method, the straightforward synthesis of multiply arylated structures has been demonstrated.
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