Published in Nat Prod Rep on April 04, 2014
Two-step enzymatic synthesis of 6-deoxy-L-psicose. Tetrahedron Lett (2016) 0.75
Mapping the reactivity and selectivity of 2-azidofucosyl donors for the assembly of N-acetyl fucosamine containing bacterial oligosaccharides. J Org Chem (2017) 0.75
Metabolic glycoengineering bacteria for therapeutic, recombinant protein, and metabolite production applications. Glycoconj J (2015) 0.75
Regioselective one-pot protection of carbohydrates. Nature (2007) 1.87
Synthesis of heparin oligosaccharides. J Am Chem Soc (2004) 1.41
Efficient, one-pot syntheses of biologically active alpha-linked glycolipids. Chem Commun (Camb) (2007) 1.34
One-pot syntheses of immunostimulatory glycolipids. J Org Chem (2010) 1.13
Synthesis of 48 disaccharide building blocks for the assembly of a heparin and heparan sulfate oligosaccharide library. Org Lett (2006) 0.99
Facile Cu(OTf)2-catalyzed preparation of per-O-acetylated hexopyranoses with stoichiometric acetic anhydride and sequential one-pot anomeric substitution to thioglycosides under solvent-free conditions. J Org Chem (2003) 0.93
Regioselective one-pot protection of glucose. Nat Protoc (2008) 0.90
A concise synthesis of tetrahydroxy-LCB, alpha-galactosyl ceramide, and 1,4-dideoxy-1,4-imino-L-ribitol via D-allosamines as key building blocks. J Org Chem (2006) 0.89
Cu(OTf)2 as an efficient and dual-purpose catalyst in the regioselective reductive ring opening of benzylidene acetals. Angew Chem Int Ed Engl (2005) 0.87
Expeditious synthesis of bacterial, rare sugar building blocks to access the prokaryotic glycome. Org Biomol Chem (2013) 0.80
Synthesis of a C-glycoside analogue of β-galactosyl ceramide, a potential HIV-1 entry inhibitor. J Org Chem (2013) 0.80
Synthesis of β-C-galactosyl D- and L-alanines. Org Biomol Chem (2012) 0.80
Rapid transformation of D-mannose into orthogonally protected D-glucosamine and D-galactosamine thioglycosides. J Org Chem (2011) 0.80
Development of sodium-dependent glucose co-transporter 2 inhibitors as potential anti-diabetic therapeutics. Curr Top Med Chem (2011) 0.79
Synthesis of maradolipid. J Org Chem (2011) 0.77
Orthogonally protected D-galactosamine thioglycoside building blocks via highly regioselective, double serial and double parallel inversions of β-D-thiomannoside. Org Biomol Chem (2013) 0.77
Synthesis of orthogonally protected bacterial, rare-sugar and D-glycosamine building blocks. Nat Protoc (2013) 0.76
Regioselective glycosylation of neamine core: a facile entry to kanamycin B related analogues. Org Lett (2004) 0.76
Expeditious synthesis of Mycobacterium tuberculosis sulfolipids SL-1 and Ac2SGL analogues. Org Lett (2014) 0.75
Synthesis of alginate oligosaccharides containing L-guluronic acids. Chem Asian J (2009) 0.75
First synthesis of Bacillus cereus Ch HF-PS cell wall trisaccharide repeating unit. Org Lett (2014) 0.75
Concise synthesis of α-galactosyl ceramide from D-galactosyl iodide and D-lyxose. Carbohydr Res (2012) 0.75
From D-glucose to biologically potent L-hexose derivatives: synthesis of alpha-L-iduronidase fluorogenic detector and the disaccharide moieties of bleomycin A2 and heparan sulfate. Chemistry (2004) 0.75
Desymmetrization of trehalose via regioselective DIBAL reductive ring opening of benzylidene and substituted benzylidene acetals. Org Biomol Chem (2013) 0.75
Synthesis of hemagglutinin-binding trisaccharides. Adv Exp Med Biol (2011) 0.75
Chemical synthesis of asparagine-linked archaeal N-glycan from Methanothermus fervidus. Chemistry (2014) 0.75