99336-46-6Relevant articles and documents
Thermal Rearrangement of Benzisoxazole- and Naphthisoxazolequinones in Solution and in the Solid State. Stereoselective Synthesis of γ-Cyanomethylidenebutenolides.
Martinez-Diaz, M. Victoria,Rodriguez-Morgade, Salome,Schaefer, Wolfram,Torres, Tomas
, p. 2261 - 2274 (2007/10/02)
Readily accessible benzisoxazolequinones 1 undergo thermal induced highly stereoselective rearrangement in solution to afford quantitatively γ-cyanomethylidenebutenolides 3.The transformation can be explained by the formation of a vinylogous nitrene inter
Quninone Chemistry. Synthesis of 3-Dialkylsulfoximido- and 2-Dialkylsulfimido-3-carbomethoxy-1,4-benzo- and Naphthoquinone Derivatives
Torres, Tomas,Eswaran, S.V.,Schaefer, Wolfram
, p. 701 - 704 (2007/10/02)
3-Methoxybenzisoxazole-4,7-quinones 1 and naphthisoxazole-4,9-quinone 4 react with dimethyl sulfoxides to give sulfoximidoquinones 2 and 5, sulfimidoquinones 8 and 11 respectively as major products.