40246-34-2Relevant articles and documents
Stereospecific access to β-mannosides from glucose-derived 1,2-orthoesters as glycosyl donors
Kaji, Eisuke,Hosokawa, Yugo,Watanabe, Yusuke,Kobayashi, Mina,Yamakawa, Mayumi
, p. 459 - 470 (2007/10/03)
A new, stereospecific synthesis of β-mannosides from glucose-derived 1,2-orthoesters has been developed by a simple four step procedure, comprising β-specific glycosidation of the 1,2-orthoesters, 2′-O-deacetylation, 2′-O-triflation, and SN 2 type inversi
3,4,6-Tri-O-benzyl-α-D-arabino-hexopyranos-2-ulosyl Bromide: A Versatile Glycosyl Donor for the Efficient Generation of β-D-Mannopyranosidic Linkages
Lichtenthaler, Frieder W.,Schneider-Adams, Thomas
, p. 6728 - 6734 (2007/10/02)
An expedient four-step sequence is described for the conversion of acetobromoglucose into the title 2-oxohexosyl ("ulosyl") bromide 4.Due to its O-benzyl protection, 4 is considerably more reactive than its acylated analogs 1-3: Ag2CO3-promoted glycosidat