1,3-Dipolar cycloaddition of 1-substituted 3,3,3-trifluoropropenes to ethyl cyanocarboxylate N-oxide

Autor:	Yuriy N. Markitanov, Vadim M. Timoshenko, Yuriy G. Shermolovich
Rok vydání:	2018
Předmět:	Sulfonyl chemistry.chemical_classification Trifluoromethyl 010405 organic chemistry Organic Chemistry Thermal decomposition Oxide Substituent 010402 general chemistry 01 natural sciences Medicinal chemistry Cycloaddition 0104 chemical sciences chemistry.chemical_compound chemistry 1 3-Dipolar cycloaddition Sulfamide
Zdroj:	Chemistry of Heterocyclic Compounds. 54:89-92
ISSN:	1573-8353 0009-3122
DOI:	10.1007/s10593-018-2236-8
Popis:	3,3,3-Trifluoropropene derivatives containing a sulfonyl, sulfoximine, or sulfamide substituent at position 1 were used in 1,3-dipolar cycloaddition reaction with ethyl cyanocarboxylate N-oxide generated by thermal decomposition of ethyl oximinochloroacetate, resulting in the formation of isomeric 4(5)-substituted ethyl 5(4)-(trifluoromethyl)-4,5-dihydroisoxazole-3-carboxylates and ethyl 4-(trifluoromethyl) isoxazole-3-carboxylate.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::e7e6b786883f3f7cb95c4763af2e31f9 https://doi.org/10.1007/s10593-018-2236-8 Zobrazit plný text záznamu Plný text ve formátu PDF Plný text ve formátu HTML
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