*DARSTELLUNG VON CARBONSAUREN DER STILBENREIHE - UBER OESTROGENE CARBONSAUREN .6.

[1] Oestrogenic activity of anol; A highly active phenol isolated from the by-products [J]. NATURE, 1938, 142 : 1121 - 1121

[2] DODDS E. C., 1939, PROC ROY SOC SET B BIOL SCI, V127, P140, DOI 10.1098/rspb.1939.0015

[3] Molecular structure in relation to oestrogenic activity. Compounds without a phenanthrene nucleus [J]. PROCEEDINGS OF THE ROYAL SOCIETY SERIES B-BIOLOGICAL SCIENCES, 1938, 125 (839): : 222 - 232

[4] Girard A, 1936, HELV CHIM ACTA, V19, P1096

[5] Two ketones of the stilboestrol group [J]. JOURNAL OF THE CHEMICAL SOCIETY, 1941, : 744 - 747

[6] KERSCHBAUM E, 1939, NATURWISSENSCHAFTEN, V27, P131

[7] LACASSAGNE A, 1946, EXPERIENTIA, V2, P70

[8] Synthetic compounds possessing biological activity similar to that of deoxycorticosterone [J]. NATURE, 1941, 148 : 595 - 595

[9] NEHER R, 1945, HELV CHIM ACTA, V28, P1506

[10] Functional variants of diethylstilbestrol [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1944, 66 : 1948 - 1950

[1] Oestrogenic activity of anol; A highly active phenol isolated from the by-products [J]. NATURE, 1938, 142 : 1121 - 1121

[2] DODDS E. C., 1939, PROC ROY SOC SET B BIOL SCI, V127, P140, DOI 10.1098/rspb.1939.0015

[3] Molecular structure in relation to oestrogenic activity. Compounds without a phenanthrene nucleus [J]. PROCEEDINGS OF THE ROYAL SOCIETY SERIES B-BIOLOGICAL SCIENCES, 1938, 125 (839): : 222 - 232

[4] Girard A, 1936, HELV CHIM ACTA, V19, P1096

[5] Two ketones of the stilboestrol group [J]. JOURNAL OF THE CHEMICAL SOCIETY, 1941, : 744 - 747

[6] KERSCHBAUM E, 1939, NATURWISSENSCHAFTEN, V27, P131

[7] LACASSAGNE A, 1946, EXPERIENTIA, V2, P70

[8] Synthetic compounds possessing biological activity similar to that of deoxycorticosterone [J]. NATURE, 1941, 148 : 595 - 595

[9] NEHER R, 1945, HELV CHIM ACTA, V28, P1506

[10] Functional variants of diethylstilbestrol [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1944, 66 : 1948 - 1950