## Abstmct: The a@ sub&umts at positions 4 and 6 do not erert observable &unmic cffcts on the ting-chain tautomeric mtios of 2,4-or 2,6-aTaqbubstituted-tetmhydm-1,~~. On the other hand, the ekaivnic @ect of the Z-a~yl subs&em is mat&& in all eight seties s&die4 the equilibria CM be desctibed @ the
The effect of hydrogen bonding on the ring-chain tautomerism of oxazolidines
✍ Scribed by Joseph V. Paukstelis; Robert M. Hammaker
- Publisher
- Elsevier Science
- Year
- 1968
- Tongue
- French
- Weight
- 185 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
It is well known that oxazolidines
and Schiff bases are in mobile equilibrium in solution
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