86883-42-3Relevant articles and documents
Synthesis of glyceryl glycosides related to A-type prymnesin toxins
Hems, Edward S.,Nepogodiev, Sergey A.,Rejzek, Martin,Field, Robert A.
, p. 14 - 23 (2018)
A suite of glycosylated glycerol derivatives representing various fragments of the glycosylated ichthyotoxins called prymnesins were chemically synthesised. Glycerol was used to represent a small fragment of the prymnesin backbone, and was glycosylated at
A CONVENIENT, ONE-STEP, HIGH-YIELD REPLACEMENT OF AN ANOMERIC HYDROXYL GROUP BY A FLUORINE ATOM USING DAST. PREPARATION OF GLYCOSYL FLUORIDES.
Posner, Gary H.,Haines, Stephen R.
, p. 5 - 8 (2007/10/02)
The anomeric hydroxyl group of various furanose and pyranose hemiacetals can be replaced by a fluorine atom stereoselectively, conveniently, mildly, and on gram-scale using DAST in THF at room temperature.
STEREOSELECTIVE SYNTHESIS OF 1,2-CIS-GLYCOFURANOSIDES USING GLYCOFURANOSYL FLUORIDES
Mukaiyama, Teruaki,Hashimoto, Yukihiko,Shoda, Shin-ichiro
, p. 935 - 938 (2007/10/02)
1,2-cis-Ribofuranosides are stereoselectively synthesized in high yields by the reaction of β-ribofuranosyl fluoride and alkohols in the presence of stannous chloride and trityl perchlorate.Under similar condition, α-arabinofuranosyl fluoride reacts with