New cyclization of N-hydroxyiminoyl chlorides with N-alkryl ethynesulfonamides: Synthesis of 4-alkyl-3-aryl-4,5-dihydro-1,5,2,4-oxathiadiazepine-5,5-diones

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N-Hydroxyiminoyl chlorides reacted With N-alkyl ethynesulfonamides in the presence of triethylamine in CH,CZ, to afford the 4-alkyl-3-aryl-4,5dihydro-1,5,2,4-oxathiadiazepine-5, 5-diones (3) as the major products together with N-alkyl-3-aryl-5-isoxazolesulfonamides (4). (C) 1999 John Wiley & Sons, Inc.
Publisher
JOHN WILEY SONS INC
Issue Date
1999
Language
English
Article Type
Article
Keywords

NITRILE OXIDES; CYCLO-ADDITIONS; 1,3-DIPOLAR CYCLOADDITIONS; REGIOCHEMISTRY; SELECTIVITY

Citation

HETEROATOM CHEMISTRY, v.10, no.6, pp.461 - 464

ISSN
1042-7163
DOI
10.1002/(SICI)1098-1071(1999)10:6<461::AID-HC4>3.0.CO;2-7
URI
http://hdl.handle.net/10203/67940
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