Pure and Applied Chemistry

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• Mohareb Rafat M., Al Farouk Fatma O., Sherif Sherif M., Karaghiosoff Konstantin: Synthesis of progesterone derivatives and evaluation of their efficiency as pneumococcal vaccines. Med Chem Res 2014. <http://dx.doi.org/10.1007/s00044-013-0894-8>
• Ibrahim-Ouali Malika, Hamze Khalil: A click chemistry approach to secosteroidal macrocycles. Steroids 2014, 80, 102. <http://dx.doi.org/10.1016/j.steroids.2013.12.002>
• Cmoch Piotr, Korda Anna, Rárová Lucie, Oklešťková Jana, Strnad Miroslav, Luboradzki Roman, Pakulski Zbigniew: Synthesis and structure–activity relationship study of cytotoxic lupane-type 3β-O-monodesmosidic saponins with an extended C-28 side chain. Tetrahedron 2014, 70, 2717. <http://dx.doi.org/10.1016/j.tet.2014.03.006>
• Strehl Cindy, Buttgereit Frank: Unraveling the functions of the membrane-bound glucocorticoid receptors: first clues on origin and functional activity. Ann. N.Y. Acad. Sci. 2014, n/a. <http://dx.doi.org/10.1111/nyas.12364>
• Ibrahim-Ouali Malika, Romero Eugénie: Synthesis of various secosteroidal macrocycles by ring-closing metathesis. Steroids 2013, 78, 651. <http://dx.doi.org/10.1016/j.steroids.2013.03.004>
• Zheng Qi-Chang, Chen Guo-Dong, Kong Ming-Zhu, Li Guo-Qiang, Cui Jia-Yu, Li Xiao-Xia, Wu Zu-Yan, Guo Liang-Dong, Cen Ying-Zhou, Zheng Yi-Zhi, Gao Hao: Nodulisporisteriods A and B, the first 3,4-seco-4-methyl-progesteroids from Nodulisporium sp. Steroids 2013, 78, 896. <http://dx.doi.org/10.1016/j.steroids.2013.05.007>
• Mohareb Rafat M., El-Sayed Nahed N.E., Abdelaziz Mahmoud A.: The Knoevenagel reactions of pregnenolone with cyanomethylene reagents: Synthesis of thiophene, thieno[2,3-b]pyridine, thieno[3,2-d]isoxazole derivatives of pregnenolone and their in vitro cytotoxicity towards tumor and normal cell lines. Steroids 2013, 78, 1209. <http://dx.doi.org/10.1016/j.steroids.2013.08.007>
• Feng Shu-Xiao, Zhang Ya-Dong: One-pot efficient synthesis of 13(R),14(R)-epoxy-17β-methyl-20(S)-hydroxyl-18-nor-pregna-4-en-3-one via a tandem epoxidation-rearrangement-epoxidation reaction sequence. Steroids 2013, 78, 1332. <http://dx.doi.org/10.1016/j.steroids.2013.10.002>
• Heasley Brian: Chemical Synthesis of the Cardiotonic Steroid Glycosides and Related Natural Products. Chem. Eur. J. 2012, 18, 3092. <http://dx.doi.org/10.1002/chem.201103733>
• Ibrahim-Ouali Malika, Romero Eugénie, Hamze Khalil: Stereoselective synthesis of pentacyclic steroids functionalized at C-11. Steroids 2012, 77, 1092. <http://dx.doi.org/10.1016/j.steroids.2012.04.004>
• Mohareb Rafat M., Wardakhan Wagnat W., Elmegeed Gamal A., Ashour Rehab M.S.: Heterocyclizations of pregnenolone: Novel synthesis of thiosemicarbazone, thiophene, thiazole, thieno[2,3-b]pyridine derivatives and their cytotoxicity evaluations. Steroids 2012, 77, 1560. <http://dx.doi.org/10.1016/j.steroids.2012.09.004>
• Mohareb Rafat M., Al-Omran Fatima: Reaction of pregnenolone with cyanoacetylhydrazine: Novel synthesis of hydrazide–hydrazone, pyrazole, pyridine, thiazole, thiophene derivatives and their cytotoxicity evaluations. Steroids 2012, 77, 1551. <http://dx.doi.org/10.1016/j.steroids.2012.09.007>
• Bullock Sam, Hallett Andrew J., Harding Lindsay P., Higginson Joshua J., Piela Sean A. F., Pope Simon J. A., Rice Craig R.: Luminescent rhenium fac-tricarbonyl-containing complexes of androgenic oxo-steroids. Dalton Trans. 2012, 41, 14690. <http://dx.doi.org/10.1039/c2dt31476b>
• Heasley Brian: Synthesis of Limonoid Natural Products. Eur J Org Chem 2011, 2011, 19. <http://dx.doi.org/10.1002/ejoc.201001218>
• D'Apolito Oceania, Garofalo Daniela, Paglia Giuseppe, Dello Russo Antonio, Corso Gaetano: Profiling of acylcarnitines and sterols from dried blood or plasma spot by atmospheric pressure thermal desorption chemical ionization (APTDCI) tandem mass spectrometry. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS 2011, 1811, 669. <http://dx.doi.org/10.1016/j.bbalip.2011.05.009>
• Mohareb Rafat M., Elmegeed Gamal A., Abdel-Salam Omar M.E., Doss Senot H., William Marian G.: Synthesis of modified steroids as a novel class of non-ulcerogenic, anti-inflammatory and anti-nociceptive agents. Steroid 2011, 76, 1190. <http://dx.doi.org/10.1016/j.steroids.2011.05.011>
• Phillips Katherine M., Ruggio David M., Horst Ronald L., Minor Bart, Simon Ryan R., Feeney Mary Jo, Byrdwell William C., Haytowitz David B.: Vitamin D and Sterol Composition of 10 Types of Mushrooms from Retail Suppliers in the United States. J AGRIC FD CHEM 2011, 59, 7841. <http://dx.doi.org/10.1021/jf104246z>
• Pd-katalysierte Synthesen Vitamin-D-aktiver Verbindungen. Nachr Chem Tech Lab 2010, 42, 394. <http://dx.doi.org/10.1002/nadc.19940420416>
• Rodrigues Oscar E.D., de Souza Diego, Soares Letiére C., Dornelles Luciano, Burrow Robert A., Appelt Helmoz R., Alves Camila F., Alves Diego, Braga Antonio L.: Stereoselective synthesis of selenosteroids. Tetrahetron Lett 2010, 51, 2237. <http://dx.doi.org/10.1016/j.tetlet.2010.02.090>
• Tabatabaeian Khalil, Mamaghani Manouchehr, Mahmoodi Nosratollah, Khorshidi Alireza: Diastereoselective Ruthenium-Catalyzed Michael Addition of Indoles to Hormone Steroids: An Efficient Route to New Indole Derivatives. Synth Comm 2010, 40, 1677. <http://dx.doi.org/10.1080/00397910903161678>
• Mohamed Nadia R., Elmegeed Gamal A., Abdelhalim Mervat M., Rady Hanaa M.: Facile Synthesis and in Vitro Cytotoxic Evaluation of Novel Thiadiazole, Pyrazole, and Dithiole-Androstane Derivatives. Phosphorus Sulfur Silicon Relat Elem 2010, 185, 848. <http://dx.doi.org/10.1080/10426500903008914>
• Streck Georg: Chemical and biological analysis of estrogenic, progestagenic and androgenic steroids in the environment. Trends in Analytical Chemistry 2009, 28, 635. <http://dx.doi.org/10.1016/j.trac.2009.03.006>
• Martinengo Marina, Ardenghi Diego Fabio, Tripodi Gino, Reali Giorgio: The first case of drug-induced immune hemolytic anemia due to hydrocortisone. Transfusion (Malden) 2008, 48, 1925. <http://dx.doi.org/10.1111/j.1537-2995.2008.01797.x>
• Moman Edelmiro, Nicoletti Daniel, Mouriño Antonio: Strained Polycycles by H⁵C^5x Free-Radical Cascades^†. Org Lett 2006, 8, 1249. <http://dx.doi.org/10.1021/ol060231w>
• Schomburg Dietmar: Nomenklatur der Lignane und Neolignane. Angew Chem 2005, 117, 2339. <http://dx.doi.org/10.1002/ange.200462947>
• Hellwich Karl-Heinz: Erweiterung und Revision des von-Baeyer-Systems zur Benennung polycyclischer Verbindungen (einschlie��lich bicyclischer Verbindungen). Angew Chem 2002, 114, 3423. <http://dx.doi.org/10.1002/1521-3757(20020902)114:17<3423::AID-ANGE3423>3.0.CO;2-6>
• Cabrera-Vivas B.M, Ram����rez J.C, Mart����nez-Aguilera L.M.R, Kubli-Garfias C: Theoretical assessment of the mechanisms involved in the cholesterol biosynthesis from lanosterol. Journal of Molecular Structure: THEOCHEM 2002, 584, 5. <http://dx.doi.org/10.1016/S0166-1280(02)00024-6>