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Cycloaddition route to 14,17-ethano- and 14-alkyl-19-norsteroids . James R. Bull, Russell I. Thomson
, J. Chem. Soc., Perkin Trans. 1
, 1990
, 241
New selenosteroids as antiproliferative agents . Alma Fuentes-Aguilar, Laura L. Romero-Hernández, Ailed Arenas-González, Penélope Merino-Montiel, Sara Montiel-Smith, Socorro Meza-Reyes, José Luis Vega-Báez, Gabriela B. Plata, José M. Padrón, Óscar López, José G. Fernández-Bolaños
, Org. Biomol. Chem.
, 2017
, 15
, 5041
Regioselective synthesis of 2-chloromercurio-estradiol and -estrone derivatives: a novel approach to A -ring substituted estrogens . Enzo Santaniello, Alberto Fiecchi, Patrizia Ferraboschi, Manuela Ravasi
, J. Chem. Soc., Perkin Trans. 1
, 1983
, 2765
Steroidal heterocycles: synthesis and structure of imidazo[2,1-b ]thiazolo-, thiazolo[3,2-a ]benzimidazolo-, and thiazolo[3,2-b ]-s -triazolo-derivatives . Joginder S. Bajwa, Peter J. Sykes
, J. Chem. Soc., Perkin Trans. 1
, 1980
, 2146
Synthesis, crystal and molecular structure of a 1,11-etheno-steroid: 3-methoxy-1,11-ethenoestra-1,3,5(10),9(11)-tetraen-17-one . Colin G. Pitt, Douglas H. Rector, David H. White, Mansukh C. Wani, Andrew T. McPhail, Kay D. Onan
, J. Chem. Soc., Perkin Trans. 1
, 1977
, 1144
Microwave-assisted one-pot synthesis of steroid–quinoline hybrids and an evaluation of their antiproliferative activities on gynecological cancer cell lines . Ádám Baji, András Gyovai, János Wölfling, Renáta Minorics, Imre Ocsovszki, István Zupkó, Éva Frank
, RSC Adv.
, 2016
, 6
, 27501
New steroidal heterocycles: synthesis and structure of androst-4-eno[3,2-f ]-(s -triazolo[4,3-b ]pyridazine), androstano[17,16-f ]-(s -triazolo[4,3-b ]pyridazines), and 2-(1,2,4-triazol-4-ylaminomethylene)-3-(1,2,4-triazol-4-ylamino)-5α-androst-2-ene . Joginder S. Bajwa, Peter J. Sykes
, J. Chem. Soc., Perkin Trans. 1
, 1979
, 1816
Manganese-catalyzed hydrogenation, dehydrogenation, and hydroelementation reactions . Kuhali Das, Satyadeep Waiba, Akash Jana, Biplab Maji
, Chem. Soc. Rev.
, 2022
, 51
, 4386
1048. Spectra and stereochemistry. Part VI. A novel cleavage of ring D during dehydrogenation of œstrone methyl ether . A. D. Cross, H. Carpio, P. Crabbé
, J. Chem. Soc.
, 1963
, 5539
A mild two-step propargylation of aromatic bioactive small molecules . Naoki Kanoh, Toshitaka Okamura, Takahiro Suzuki, Yoshiharu Iwabuchi
, Org. Biomol. Chem.
, 2017
, 15
, 7190