Steroid alcohols with semi-cyclic double compounds

[1] BERTRAM J, 1894, J PR, V49, P192

[2] GOULD RG, 1935, AM SOCIOL, V57, P340

[3] INHOFFEN HH, 1938, Z ANGEW CH, V51, P173

[4] Kathol J., 1937, NATURWISSENSCHAFTEN, V25, P682

[5] LOGEMANN W, 1938, NATURWISSENSCHAFTEN, V26, P840

[6] On the presentation of progesterone and neo-progesterone from dehydro-androsterone [J]. HELVETICA CHIMICA ACTA, 1939, 22 : 184 - 195

[7] The cultivation of lateral chains of t-dehydro-androsteron [J]. HELVETICA CHIMICA ACTA, 1938, 21 : 1317 - 1326

[8] MIESCHER K, 1938, CHEM IND, V57, P276

[9] RUZICKA J, 1923, HELV CHIM ACTA, V6, P492

[10] Se hormones XXIV. On the disposition of acetylene in the 17-constant keto group of trans-androsterone and Delta(5)-trans-dehydro-androsterone [J]. HELVETICA CHIMICA ACTA, 1937, 20 : 1280 - 1282

[1] BERTRAM J, 1894, J PR, V49, P192

[2] GOULD RG, 1935, AM SOCIOL, V57, P340

[3] INHOFFEN HH, 1938, Z ANGEW CH, V51, P173

[4] Kathol J., 1937, NATURWISSENSCHAFTEN, V25, P682

[5] LOGEMANN W, 1938, NATURWISSENSCHAFTEN, V26, P840

[6] On the presentation of progesterone and neo-progesterone from dehydro-androsterone [J]. HELVETICA CHIMICA ACTA, 1939, 22 : 184 - 195

[7] The cultivation of lateral chains of t-dehydro-androsteron [J]. HELVETICA CHIMICA ACTA, 1938, 21 : 1317 - 1326

[8] MIESCHER K, 1938, CHEM IND, V57, P276

[9] RUZICKA J, 1923, HELV CHIM ACTA, V6, P492

[10] Se hormones XXIV. On the disposition of acetylene in the 17-constant keto group of trans-androsterone and Delta(5)-trans-dehydro-androsterone [J]. HELVETICA CHIMICA ACTA, 1937, 20 : 1280 - 1282