The reaction of cyclic enol ethers with arenesulfonyl azides. A new ring contraction reaction. Ring expansion and ring contraction reactions by means of diazonium betaines. II.
β Scribed by Ronald A. Wohl
- Publisher
- Elsevier Science
- Year
- 1973
- Tongue
- French
- Weight
- 194 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
We would like to report a new general ring contraction reaction according to the following scheme (eq. l(a),R = ArSO,): The enol ether la derived from a cyclic ketone is reacted with a suitable aside leading via an intermediate unstable 6'-triazoline & to the ring-contracted imidate ester 3a.
π SIMILAR VOLUMES
By use of cesium fluoride as a catalyst, aryl or alkyl glycidyl ethers were ring-opened by aryl trimethylsilyl ether to produce O-protected aryloxyhydrins with a quantitative regioselectivity for the first time. Alkyl silyl ether was ineffective for this ring-opening. Hy the regioselective ring-ope
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