期刊
ORGANIC LETTERS
卷 14, 期 18, 页码 4842-4845出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol302168q
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资金
- Japan Private School Promotion Foundation
- MEXT
- CCIS
- Grants-in-Aid for Scientific Research [24590025] Funding Source: KAKEN
The combination of 1,1,3,3-tetramethyldisiloxane (TMDS) and trimethylbromosilane (Me3SiBr) with a catalytic amount of indium bromide (InBr3) undertook direct bromination of carboxylic acids, which produced the corresponding alkyl bromides in good to excellent yields. The reducing system was tolerant to several functional groups.
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