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- W2149207617 abstract "Thermolysis of 6-aryl-1,5-diazabicyclo[3.1.0]hexanes in the presence of N-arylmaleimides having a substituent in the ortho position of the aromatic ring leads to predominant formation of the corresponding trans-9-arylperhydropyrazolo[1,2-a]pyrrolo[3,4-c]pyrazole-1,3-diones. 6-Aryl-1,5-diazabicyclo[3.1.0]hexanes react with fumaric acid derivatives in a stereoselective fashion, affording perhydropyrazolo[1,2-a]pyrazoles with a trans,trans configuration." @default.
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- W2149207617 date "2004-08-17" @default.
- W2149207617 modified "2023-09-23" @default.
- W2149207617 title "Stereoselectivity in the Addition of 1,3-Dipolarophiles to 6-Aryl-1,5-diazabicyclo[3.1.0]hexanes." @default.
- W2149207617 cites W2950650026 @default.
- W2149207617 doi "https://doi.org/10.1002/chin.200433140" @default.
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