## Abstract Novel quinolines fused with a six‐member ring **5a–j** were prepared in high yields (75–95%) via the Friedländer reaction of dimethoxy‐substituted __o__‐aminobenzaldehydes of **3a** or **3b** with cyclic ketones **4**, respectively. The structures of **5a–j** were determined by IR, ^1^H
✦ LIBER ✦
Novel Six-Ring Compounds Via The Reaction of Ketene Diethylacethal with methanesulfonyl chloride
✍ Scribed by W.E. Truce; D.J. Abraham; P.S. Radhakrishnamurti
- Book ID
- 104241964
- Publisher
- Elsevier Science
- Year
- 1963
- Tongue
- French
- Weight
- 226 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0040-4039
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