The reaction of p-benzoquinone-4-oximes with disulfur dichloride affords the red 6H-1,2,3benzodithiazol-6-ones. Some ring chlorination occurs, but 2,6-substituents are retained in the products except for a ferr-butyl group, which is, exceptionally, replaced by chlorine. 1,4-Naphthoquinone 4-oxime an
β¦ LIBER β¦
Synthesis of 5-methyl-1,3,2-benzodithiazoles
β Scribed by Chin H. Chen; Barbara A. Donatelli
- Book ID
- 112125551
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1979
- Tongue
- English
- Weight
- 141 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
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