Thermal rearrangement of the endo-peroxides of the 2,5-dimethylfurans (1b) and (1c) in refluxing benzene leads to the corresponding diepoxides (4b) and (4c), which provides a convenient entry to the synthesis of these compounds which are structurally related to crotepoxide.
Unusual thermal rearrangement of the endo-peroxides of 2,5-dimethylfurans / Graziano, M. L.; Iesce, M. R.; Scarpati, R.. - In: JOURNAL OF THE CHEMICAL SOCIETY, CHEMICAL COMMUNICATIONS. - ISSN 0022-4936. - 14(1981), pp. 720-721. [10.1039/C39810000720]
Unusual thermal rearrangement of the endo-peroxides of 2,5-dimethylfurans
Graziano M. L.;Iesce M. R.;
1981
Abstract
Thermal rearrangement of the endo-peroxides of the 2,5-dimethylfurans (1b) and (1c) in refluxing benzene leads to the corresponding diepoxides (4b) and (4c), which provides a convenient entry to the synthesis of these compounds which are structurally related to crotepoxide.File in questo prodotto:
Non ci sono file associati a questo prodotto.
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
