Abstract
(graph presented) The reaction of nitroso compounds with enolates, "the nitroso aldol reaction", occurs in high yield to generate α-hydroxyamino carbonyl compounds. Yields range from 42% to 98% with N-selectivity >99:1 from commercially available aromatic or aliphatic nitroso compounds and a variety of alkali metal or tin enolates.
| Original language | English |
|---|---|
| Pages (from-to) | 3579-3582 |
| Number of pages | 4 |
| Journal | Organic letters |
| Volume | 4 |
| Issue number | 21 |
| DOIs | |
| Publication status | Published - 2002 Oct 17 |
ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry
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Cite this
Momiyama, N., & Yamamoto, H. (2002). Simple synthesis of α-hydroxyamino carbonyl compounds: New scope of the nitroso aldol reaction. Organic letters, 4(21), 3579-3582. https://doi.org/10.1021/ol026443k