期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 134, 期 2, 页码 875-877出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja210585n
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资金
- Ministry of Education, Culture, Sports, and Technology (MEXT), Japan [2105]
- Grants-in-Aid for Scientific Research [23655088, 21106003] Funding Source: KAKEN
Hydroxymethylation of alkyl halides was achieved using paraformaldehyde as a radical C1 synthon in the presence of tetrabutylammonium cyanoborohydride as a hydrogen source. The reaction proceeds via a radical chain mechanism involving an alkyl radical addition to formaldehyde to form an alkoxy radical, which abstracts hydrogen from a hydroborate anion.
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