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2-Methoxy- and 2-ethoxy-1-arylsulfonylaziridines, which are formed by reaction of arenesulfrayl azides with methyl and ethyl vinyl ethers, react with ketones to give 5-alkoxy-2,2-dialkyl-3-arylsulfonyloxazolidines, along with products of dimerization and polymerization of the alkoxyaziridines.Communication V from the series Reaction of Organic Azides with Unsaturated Compounds; see [1] for communication IV. The results of this study are protected by an author's certificate [2].Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1613–1618, December, 1976.  相似文献   
2.
2-Methyl-1-arylsulfonylaziridines, formed in the reaction of tosyl and p-nitrobenzenesulfonyl azides with methyl vinyl ether, react regiospecifically with ,-unsaturated aldehydes and ketones to give 5-methoxy-2-vinyl-3-arylsulfonyloxazolidines. The effect of the structure of the aziridines and unsaturated aldehydes and ketones on the stereoselectivity of their reactions is discussed.Communication VII of the series Reaction of organic azides with unsaturated compounds. See [1] for communication VI. The results of this research are protected by an author's certificate [2].Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 332–336, March, 1977.  相似文献   
3.
trans-2-Alkyl- and trans-2-aryl-5-methoxy-3-tosyloxazolidines are formed in the reaction of tosyl azide with methyl vinyl ether in the presence of aldehydes.Communication VI from the series Reaction of Organic Azides with Unsaturated Compounds; see [1] for communication V. The results of this study are protected by an author's certificate [2].Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 27–29, January, 1977.  相似文献   
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