Abstract Treatment of 2-pivaloyl-1, 3-indandione (1) with hydroxylamine under acidic conditions, results in formation of 8-t-butylindeno [1, 2-c] isoxazol-7-one (2) while treatment of the triketone with hydroxylamine at neutral or basic pH gave 6 which upon cyclization gave the isomeric 3-t-butylindeno [1, 2-c] isoxazol-4-one (7). Compound 7 was readily reduced to amine 12 by treatment with hydrazine or hydrogen over platinum. The amine, ...
![(E)-3-(tert-butyl)-4H-indeno[1,2-c]isoxazol-4-one oxime结构式](https://image.chemsrc.com/caspic/268/82501-29-9.png)
![6,13-di-tert-butyl-4b,6,11b,13-tetrahydrodiindeno[1,2-b:1',2'-f][1,5]dioxocine-4b,6,7,11b,13,14-hexaol结构式](https://image.chemsrc.com/caspic/365/82501-31-3.png)
