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Org Lett ; 22(7): 2702-2706, 2020 Apr 03.
Artigo em Inglês | MEDLINE | ID: mdl-32174117

RESUMO

Unprecedented three-dimensional 1,2,6-thiadiazine 1-oxides have been prepared by an aza-Michael-addition/cyclization/condensation reaction sequence starting from sulfonimidamides and propargyl ketones. The products have been further functionalized by standard cross-coupling reactions, selective bromination of the heterocyclic ring, and conversion into a ß-hydroxy substituted derivative. A representative product was characterized by single-crystal X-ray structure analysis.

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