130995-73-2Relevant academic research and scientific papers
A mild and efficient method for the chemoselective deprotection of acetonides with lanthanum(III) nitrate hexahydrate
Malla Reddy,Venkat Reddy,Venkateswarlu
, p. 7439 - 7441 (2005)
Acetonides are hydrolyzed selectively and efficiently with lanthanum(III) nitrate hexahydrate in acetonitrile. The method has good compatibility with other sensitive hydroxyl protecting groups such as trityl, TBDMS, THP, OAc, OBz and OBn.
The role of the C-3 substituent in the asymmetric dihydroxylation of hexo-5-enofuranosides
Mereyala, Hari Babu,Goud, P. Mallikarjun,Gadikota, Rajendrakumar Reddy,Maddala, Rama Krishna,Reddy, K. Ramasubba
, p. 1201 - 1210 (2007/10/03)
Asymmetric dihydroxylation of vinyl furanosides 1-6 by use of OsO4, AD-mix-α and β is described yielding the corresponding hexofuranose sugars. Vinyl furanosides 2 and 3, with an ester group at C-3, and vinyl manno furanoside 5 on asymmetric dihydroxylation with AD-mix α exhibited high R diastereoselectivity at C-5. Reversal in diastereoselectivity at C-5 was observed for the 3-deoxy vinyl furanoside 6 giving furanosaccharide 6S with the S configuration at C-5.
Anthracyclinones, Part 4. The Use of DBN or DBU in a Novel Extension of the Marschalk Reaction leading to Hydroxyglycitylanthraquinones
Qureshi, Shireen,Shaw, Gordon,Burgess, E. Gillian
, p. 1557 - 1564 (2007/10/02)
Leuco-quinizarin (1) with propanal, 3-O-(p-chlorobenzyl)-(or 3-O-acetyl)-1,2-O-isopropylidene-α-D-xylo-pentodialdo-1,4-furanose (6a) or (6c), or 3-O-acetyl-3-C-ethynyl-1,2-O-isopropylidene-α-D-ribo-pentodialdo-1,4-furanose (6b) in dimethylformamide soluti
