## Abstract Structure elucidation of compounds in the benzisoxazole series (**1**β**6**) and naphtho[1,2β__d__][1,3]β (**7**β**10**) and phenanthro[9,10β__d__][1,3]oxazole (**11**β**14**) series was accomplished using extensive 2D NMR spectroscopic studies including ^1^Hβ^1^H COSY, longβ range ^1^H
Photolytic closure of 4,5-diphenyl-oxazol-2-ones to phenanthro[9,10-d]oxazol-2-ones and an improved synthesis of benzoins
β Scribed by Gholamhosein H. Hakimelahi; Charles B. Boyce; Hamid S. Kasmai
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- German
- Weight
- 357 KB
- Volume
- 60
- Category
- Article
- ISSN
- 0018-019X
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β¦ Synopsis
Abstract
The synthesis of phenathrenes substituted by nitrogen and oxygen atoms in position 9 and 10 by photolysis of 4,5βdiphenylβoxazolβ2βones (cf. Scheme 4) is described. Moreover an improved general procedure for the synthesis of benzoins in aprotic solvent (tetraβtβbutylammonium cyanide in DMF/DMSO) is developed.
π SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
The titZe quinarenone 2 has been prepared and proved that the three-membered ring possesses a larger diatropicity than diphenyZcycZopropenone and the seven-membered ring exists in a cycloheptatriene (not norcaradienel tautomer having a contribution of a homobenzene structure. The rotational barrier