Tautomerism of aromatic [j-ketoaldehydes p-XPhCO-CHzCHO (1, X = NMe,, OMe, Me, H, Br, NOz), aliphatic B-ketoaldehydes and benzoylacetaldehyde RCOCH,CHO (2, R = Me, i-Bu, f-Bu, Ph), RCOCH(Me)CHO (3, R = Me, Et, i-Pr) and methyl 2-formylpropionate MeOCOCH(Me)CHO (4) has been studied by the 'H NMR tech
✦ LIBER ✦
Tautomeric equilibrium of ketonic and cis- and trans-enolic forms of β-dicarbonyl compounds in solution
✍ Scribed by M.I. Kabachnik; S.T. Yoffe; K.V. Vatsuro
- Publisher
- Elsevier Science
- Year
- 1957
- Tongue
- French
- Weight
- 678 KB
- Volume
- 1
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
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