
Monatshefte fur Chemie p. 371 - 381 (1991)
Update date:2022-07-29
Topics:
Neidlein, Richard
Bischer, Alfred
N-alkylated 2,5-diamino-p-benzoquinone-3,6-dicarboacidamides 6 and 7 are synthezised by alkylation and following reduction of 3,7-diamino-substituted benzodiisoxazolidiones 1c-f.Quinoneheterocycles 2a-b react under the presence of amines in a similar way to dioxobenzodiisoxazolium-salts 3 and 4 via intermediate formation of vinylogous, intramolecularly stabilized carbonylnitrenes to mono-, bi-, and tricycled quinone-derivatives 8, 9, 11 and 13-15.
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Doi:10.1021/om500335m
(2014)Doi:10.1002/chem.201703926
(2017)Doi:10.1134/S1070428010090125
(2010)Doi:10.1002/hlca.19910740402
(1991)Doi:10.1016/S0040-4039(00)79740-1
(1991)Doi:10.1002/adsc.201900154
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