Journal of the Chemical Society, Perkin Transactions 1
Reactions of 1-aryl-2, 2-dihalogenoethanone oximes with tetrasulfur tetranitride (S 4 N 4): a general method for the synthesis of 3-aryl-4-halogeno-1, 2, 5-thiadiazoles
SC Yoon
文献索引:Yoon, Sung Cheol; Cho, Jaeeock; Kim, Kyongtae Journal of the Chemical Society - Perkin Transactions 1, 1998 , # 1 p. 109 - 116
1-Aryl-2, 2-dichloro-7, 1-aryl-2, 2-dibromo-8, 1-aryl-2-bromo-2-fluoro-9 and 1-aryl-2-chloro-2- fluoro-ethanone oximes 10 have been prepared by allowing the corresponding ketones to react with hydroxylamine hydrochloride in EtOH at room temperature. Stereochemical assignments for the oximes were made on the basis of 1H NMR spectroscopic evidence and an X-ray crystallographic analysis of 1-(3-chlorophenyl)-2, 2-dichloroethanone oxime 7f. ...