TY - JOUR
T1 - The chemical synthesis of human milk oligosaccharides: Lacto-N-tetraose (Galβ1→3GlcNAcβ1→3Galβ1→4Glc)
AU - Bandara, Mithila D.
AU - Stine, Keith
AU - Demchenko, Alexei V.
N1 - The total chemical synthesis of lacto-N-tetraose (LNT) has been completed using both convergent and linear strategies. Similarly to that of our previo...
PY - 2019/9/22
Y1 - 2019/9/22
N2 - The total chemical synthesis of lacto- N -tetraose (LNT) has been completed using both convergent and linear strategies. Similarly to that of our previous HMO syntheses, the donor-acceptor protecting-leaving group combinations were found to be of paramount significance to achieving successful glycosylations and minimizing side reactions.
AB - The total chemical synthesis of lacto- N -tetraose (LNT) has been completed using both convergent and linear strategies. Similarly to that of our previous HMO syntheses, the donor-acceptor protecting-leaving group combinations were found to be of paramount significance to achieving successful glycosylations and minimizing side reactions.
UR - https://www.sciencedirect.com/science/article/abs/pii/S0008621519304264?via%3Dihub
UR - https://pubag.nal.usda.gov/catalog/6536343
U2 - 10.1016/j.carres.2019.107824
DO - 10.1016/j.carres.2019.107824
M3 - Article
VL - 486
JO - Carbohydrate Research
JF - Carbohydrate Research
ER -