152840-34-1Relevant articles and documents
Structural establishment of polygalatenosides A and B by total synthesis
Huang, Chih-Ming,Liu, Rai-Shung,Wu, Tian-Shung,Cheng, Wei-Chieh
, p. 2895 - 2898 (2008/09/21)
The first total synthesis of polygalatenosides A (1) and B (2), originally isolated from the traditional Chinese medicine and reported as antidepressant agents, is described here. Glycosylation between thiogalactosyl donors 6 and 7 and 1-deoxyglucosyl acc
Samarium diiodide-mediated reductive coupling of epoxides and carbonyl compounds: A stereocontrolled synthesis of C-glycosides from 1,2-anhydro sugars
Chiara, Jose Luis,Sesmilo, Esther
, p. 3242 - 3246 (2007/10/03)
Sugar mimics: 1,2-anhydro sugars can be cross-coupled with aldehydes and ketones under very mild conditions and using a wide range of protecting groups to give C-glycosides in good yield in a radical reaction mediated by SmI2 (see scheme; A = n
Synthesis of the C-glycosidic analogue of adenophostin A and its uracil congener as potential IP3 receptor ligands. Stereoselective construction of the C-glycosidic structure by a temporary silicon-tethered radical coupling reaction
Abe, Hiroshi,Shuto, Satoshi,Matsuda, Akira
, p. 4315 - 4325 (2007/10/03)
Synthesis of the C-glycosidic analogue 9 of adenophostin A, a very potent IP3 receptor agonist, and its uracil congener 10 was achieved via a temporary silicon-tethered radical coupling reaction as the key step. Phenyl 3,4,6-tri-O-(p-methoxyben