The recent unambiguom identification of the main products in the photolysis of a series of Z-phenyl-and 2-cyanoquinoline l-oxides as benzCdl-1,3-oxazepines (1) cf. ( ), has led us to
✦ LIBER ✦
Photolysis of 4-phenylquinazoline 3-oxides to benz[f]-1,3,5-oxadiazepines
✍ Scribed by Chikara Kaneko; Sachiko Yamada
- Publisher
- Elsevier Science
- Year
- 1967
- Tongue
- French
- Weight
- 224 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0040-4039
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## Abstract The model morpholine‐1‐carbothioic acid (2‐phenyl‐3__H__‐quinazolin‐4‐ylidene) amide (1) reacts with phenacyl bromides to afford __N__^4^‐(5‐aryl‐1,3‐oxathiol‐2‐yliden)‐2‐phenylquinazolin‐4‐amines (4) or __N__^4^‐(4,5‐diphenyl‐1,3‐oxathiol‐2‐yliden)‐2‐phenyl‐4‐aminoquinazoline (**5**) b