Publication | Closed Access
Glycosyl-Acceptor-Derived Borinic Ester-Promoted Direct and β-Stereoselective Mannosylation with a 1,2-Anhydromannose Donor
89
Citations
42
References
2016
Year
Mono-ol AcceptorsBioorganic Chemistryβ-Stereoselective MannosylationsBiochemistryEngineeringNatural SciencesDiversity-oriented SynthesisGlycobiologyβ-Stereoselective MannosylationTotal SynthesisOrganic ChemistryCatalysis1,2-Anhydromannose DonorChemistryStereoselective SynthesisSynthetic ChemistryEnantioselective Synthesis
β-Stereoselective mannosylations were conducted using a 1,2-anhydromannose donor and mono-ol acceptors in the presence of a glycosyl-acceptor-derived borinic ester. Reactions proceeded smoothly under mild conditions to provide the corresponding β-mannosides with high stereoselectivity in moderate to high yields. In addition, the present glycosylation method was applied successfully to the total synthesis of acremomannolipin A.
| Year | Citations | |
|---|---|---|
Page 1
Page 1