DIE REAKTION VON PENTAMETHYLPYRROL MIT WASSERSTOFFPEROXYD

[1] Synthesis of a series of alpha-substituted N-methylpyrrolines [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1933, 55 : 295 - 298

[2] MOLD METABOLITES .9. CONTRIBUTION TO ELUCIDATION OF STRUCTURE OF ALTHIOMYCIN [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1963, 85 (10) : 1430 - +

[3] EIN BISHYDROPEROXYD MIT UNGEWOHNLICHER BILDUNGSTENDENZ [J]. CHEMISCHE BERICHTE-RECUEIL, 1963, 96 (10): : 2704 - &

[4] VERSUCHE ZUR DARSTELLUNG VON TETRAMETHYL-CYCLOBUTADIEN [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1962, 74 (18) : 703 - &

[5] CRIEGEE R, 1953, LIEBIGS ANN CHEM, V583, P4

[6] DELEPINE M, 1896, BER DTSCH CHEM GES, V29, P590

[7] Synthesis of the 2,4-Dimethyl-3-ethyl-5-oxy pyrrol, as well as new synthesis of xantho bilirubic acid, for example the bilirubic acid. [J]. HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1932, 212 : 146 - 156

[8] The synthesis of biliverdine (uteroverdine) and bilirubine, biliverdine XIII alpha and III alpha, as well as vinyl neoxanthin acid [J]. HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1942, 274 : 231 - 260

[9] Synthesis of oxyhaemopyrrols, iso-neo, iso-xanthobilirubic acid and concerning cryptopyrrolether. [J]. HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1934, 226 : 116 - 129

[10] Fischer H, 1937, LIEBIGS ANN CHEM, V528, P265

[1] Synthesis of a series of alpha-substituted N-methylpyrrolines [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1933, 55 : 295 - 298

[2] MOLD METABOLITES .9. CONTRIBUTION TO ELUCIDATION OF STRUCTURE OF ALTHIOMYCIN [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1963, 85 (10) : 1430 - +

[3] EIN BISHYDROPEROXYD MIT UNGEWOHNLICHER BILDUNGSTENDENZ [J]. CHEMISCHE BERICHTE-RECUEIL, 1963, 96 (10): : 2704 - &

[4] VERSUCHE ZUR DARSTELLUNG VON TETRAMETHYL-CYCLOBUTADIEN [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1962, 74 (18) : 703 - &

[5] CRIEGEE R, 1953, LIEBIGS ANN CHEM, V583, P4

[6] DELEPINE M, 1896, BER DTSCH CHEM GES, V29, P590

[7] Synthesis of the 2,4-Dimethyl-3-ethyl-5-oxy pyrrol, as well as new synthesis of xantho bilirubic acid, for example the bilirubic acid. [J]. HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1932, 212 : 146 - 156

[8] The synthesis of biliverdine (uteroverdine) and bilirubine, biliverdine XIII alpha and III alpha, as well as vinyl neoxanthin acid [J]. HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1942, 274 : 231 - 260

[9] Synthesis of oxyhaemopyrrols, iso-neo, iso-xanthobilirubic acid and concerning cryptopyrrolether. [J]. HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1934, 226 : 116 - 129

[10] Fischer H, 1937, LIEBIGS ANN CHEM, V528, P265