288585-01-3Relevant academic research and scientific papers
Stereoselective synthesis of α- and β-C-glucosides via radical cyclization with an allylsilyl tether. Control of the stereoselectivity by changing the conformation of the pyranose ring
Shuto, Satoshi,Terauchi, Masaru,Yahiro, Yumi,Abe, Hiroshi,Ichikawa, Satoshi,Matsuda, Akira
, p. 4151 - 4155 (2000)
An efficient method for preparing both 1α- and 1β-C-glucosides having a 3-hydroxypropyl group at the anomeric position via a radical cyclization reaction with an allylsilyl tether was developed. The stereoselectivity of the radical cyclization can be cont
Synthesis of 4,8-anhydro-d-glycero-d-ido-nonanitol 1,6,7-trisphosphate as a novel IP3 receptor ligand using a stereoselective radical cyclization reaction based on a conformational restriction strategy
Terauchi, Masaru,Yahiro, Yumi,Abe, Hiroshi,Ichikawa, Satoshi,Tovey, Stephen C.,Dedos, Skarlatos G.,Taylor, Colin W.,Potter, Barry V.L.,Matsuda, Akira,Shuto, Satoshi
, p. 3697 - 3707 (2007/10/03)
4,8-Anhydro-d-glycero-d-ido-nonanitol 1,6,7-trisphosphate (9), designed as a novel IP3 receptor ligand having an α-C-glycosidic structure, was synthesized via a radical cyclization reaction with a temporary connecting allylsilyl group as the ke
