Rearrangement of 1-acetylindoxyl oxime into 1-acetyl-2-acetoxy-3-iminoindoline hydrosulfate
✍ Scribed by V. S. Velezheva; S. Yu. Ryabova; L. M. Alekseeva
- Book ID
- 104781469
- Publisher
- Springer US
- Year
- 1990
- Tongue
- English
- Weight
- 203 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0009-3122
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📜 SIMILAR VOLUMES
The chiral title compound, C 8 H 9 NO 4 , crystallizes in the noncentrosymmetric space group P2 1 2 1 2 1 , but in the absence of an atom with significant anomalous dispersion, the absolute configuration could not be determined. The H atoms in both methyl groups are eclipsed with respect to the C O
In the title compound, C 15 H 17 NO 2 , the six-membered cyclohexene ring has an envelope conformation. The structure is stabilized by O-HÁ Á ÁN hydrogen bonds and weak van der Waals interactions. There are no C-HÁ Á Á orinteractions between the two ring systems; however, there is an intermolecular