Pure Appl. Chem., 1989, Vol. 61, No. 3, pp. 431-434
http://dx.doi.org/10.1351/pac198961030431
The synthesis of brassinosteroid
CrossRef Cited-by Linking
- Wang Haixing, Su Fuqin, Zhou Liang, Chen Xiaoguang, Lei Pingsheng: Synthesis and cytotoxicities of icogenin analogues with disaccharide residues. Biorg Med Chem Lett 2009, 19, 2796. <http://dx.doi.org/10.1016/j.bmcl.2009.03.092>
- Zhang S. Q., Zhang J. S., Wang C. Z.: Synthesis of pennogenyl saponins using three methods. Chem Nat Compd 2007, 43, 422. <http://dx.doi.org/10.1007/s10600-007-0153-7>
- Zhang S. Q., Zhang J. S., Wang C. Z.: Extraction of steroid saponins from Paris polyphylla Sm. var. yunnanensis using novel ultrahigh pressure extraction technology. Pharm Chem J 2007, 41, 424. <http://dx.doi.org/10.1007/s11094-007-0092-4>
- Zhang Shouqin, Zhang Jinsong, Wang Changzheng: Synthesis of pennogenyl saponin analogs using three methods. Russ Chem Bull 2006, 55, 1856. <http://dx.doi.org/10.1007/s11172-006-0498-2>
- Zou Chuan-Chun, Hou Shu-Jie, Shi Yang, Lei Ping-Sheng, Liang Xiao-Tian: The synthesis of gracillin and dioscin: two typical representatives of spirostanol glycosides. Carbohydrates Research 2003, 338, 721. <http://dx.doi.org/10.1016/S0008-6215(03)00004-1>
- Ramı́rez Javier A, Teme Centurión Osvaldo M, Gros Eduardo G, Galagovsky Lydia R: Synthesis and bioactivity evaluation of brassinosteroid analogs. Steroid 2000, 65, 329. <http://dx.doi.org/10.1016/S0039-128X(00)00093-3>
- Deng Shaojiang, Yu Biao, Hui Yongzheng: A facile synthetic approach to a group of structurally typical diosgenyl saponins. Tetrahetron Lett 1998, 39, 6511. <http://dx.doi.org/10.1016/S0040-4039(98)01354-9>
- Centurión Osvaldo M.Teme, Galagovsky Lydia R., Gros Eduardo G.: Cleavage reaction of 5β,6β steroidal epoxides carrying different groups at C-3. Steroid 1995, 60, 434. <http://dx.doi.org/10.1016/0039-128X(95)00032-L>
- Zhou Wei-Shan, Huang Liang-Fu: Studies on steroidal plant-growth regulator 25. Concise stereoselective construction of sidechain of brassinosteroid from the intact sidechain of hyodeoxycholic acid: formal syntheses of brassinolide, 25-methylbrassinolide, 26, 27-bisnorbrassinolide and their related compounds. Tetrahedron 1992, 48, 1837. <http://dx.doi.org/10.1016/S0040-4020(01)88509-4>
- Zheng-Wu Shen, Wei-Shan Zhou: Study on the synthesis of brassinolide and related compounds: XIV. β-alkylative 1,3-carbonyl transposition of the steroidal 22-en-24-one: A new practical route to the side chain of the plant growth promoter, brassinosteroid. Chin J Chem 1990, 8, 191. <http://dx.doi.org/10.1002/cjoc.19900080216>