Lee, Juyeol; Kang, Soyeong; Kim, Jungjoon; Moon, Dohyun; Rhee, Young Ho published the artcile< A Convergent Synthetic Strategy towards Oligosaccharides containing 2,3,6-Trideoxypyranoglycosides>, Formula: C12H20O6, the main research area is palladium catalyst ring closure metathesis oligosaccharide preparation crystal structure; oligosaccharide deoxypyranoglycoside preparation stereoselective hydroalkoxylation alkoxyallene; asymmetric synthesis; carbohydrates; diastereoselectivity; oligosaccharides; palladium.
A de novo synthetic strategy for the production of oligosaccharides containing 2,3,6-trideoxypyranoglycoside is reported. The key event is the Pd-catalyzed asym. diastereoselective hydroalkoxylation of ene-alkoxyallene-linked glycosidic fragments. The utility of this approach was demonstrated by the activation-free, stereo-divergent, and convergent synthesis of various 2-deoxyoligosaccharides, as well as their aglycon conjugates.
Angewandte Chemie, International Edition published new progress about Cross-metathesis. 4064-06-6 belongs to class alcohols-buliding-blocks, and the molecular formula is C12H20O6, Formula: C12H20O6.
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts