86824-63-7Relevant academic research and scientific papers
Asymmetric epoxidation of alkenes catalyzed by a porphyrin-inspired manganese complex
Dai, Wen,Li, Jun,Li, Guosong,Yang, Hua,Wang, Lianyue,Gao, Shuang
supporting information, p. 4138 - 4141 (2013/09/12)
A novel strategy for catalytic asymmetric epoxidation of a wide variety of olefins by a porphyrin-inspired chiral manganese complex using H 2O2 as a terminal oxidant in excellent yield with up to greater than 99% ee has been successfully developed.
Semi-synthesis and biological evaluation of 1,2,3-triazole-based podophyllotoxin congeners as potent antitumor agents inducing apoptosis in HepG2 cells
Chen, Jinying,Ma, Liang,Zhang, Ronghong,Tang, Jie,Lai, Huijun,Wang, Jun,Wang, Guangcheng,Xu, Qinyuan,Chen, Tao,Peng, Fei,Qiu, Jingxiang,Liang, Xiaolin,Cao, Dong,Ran, Yan,Peng, Aihua,Wei, Yuquan,Chen, Lijuan
, p. 945 - 956 (2013/02/22)
A series of 4β-[(4-substituted)-1,2,3-triazol-1-yl]podophyllotoxin congeners were synthesized by employing click chemistry and further evaluated for their antitumor activity by MTT assay. Among them, six congeners (10, 11, 12, 13, 22, and 24) exhibited ap
Improved Synthesis of Aryl 1,1-Dimethylpropargyl Ethers
Godfrey, Jollie D.,Mueller, Richard H.,Sedergran, Thomas C.,Soundarajan, Nachimuthu,Colandrea, Vincent J.
, p. 6405 - 6408 (2007/10/02)
An efficient, general, and practical synthesis of aryl 1,1-dimethylpropargyl ethers has been developed.
A NOVEL SYNTHESIS OF 6-DEMETHOXYACRONYCINE
Elomri, Abdelhakim,Michel, Sylvie,Tillequin, Francois,Koch, Michel
, p. 799 - 806 (2007/10/02)
The title compound was synthetized in six steps, starting from 3-nitrophenol.The key-step involves condensation of 2-bromobenzoic acid with 5-amino-2,2-dimethylchromene.
Studies of Chromenes. Part 10. Oxiranes of Nitrochromenes
Brown, Philip E.,Lewis, Robert A.
, p. 573 - 578 (2007/10/02)
Syntheses of stable oxiranes of 5- and 7-nitro-, and 5,7-dinitro-2,2-dimethyl(chromenes and of 7-2H-ethoxycarbonylamino)-2,2-dimethyl-5-nitro-2H-chromene are described.Thermal cyclisation of the precursor phenyl prop-2-ynyl ethers proceeds in good yield b
