Unknown

Dataset Information

0

Chemical Synthesis of Human Milk Oligosaccharides: Lacto-N-hexaose Galβ1→3GlcNAcβ1→3 [Galβ1→4GlcNAcβ1→6] Galβ1→4Glc.


ABSTRACT: The first synthesis of lacto-N-hexaose (LNH) has been completed using a convergent strategy. The donor-acceptor protecting-leaving group combinations were found to be of paramount significance for achieving successful glycosylations and minimizing side reactions. Lacto-N-tetraose, another common human milk oligosaccharide, was also obtained en route to the target LNH.

SUBMITTER: Bandara MD 

PROVIDER: S-EPMC8114087 | biostudies-literature | 2019 Dec

REPOSITORIES: biostudies-literature

altmetric image

Publications

Chemical Synthesis of Human Milk Oligosaccharides: Lacto-<i>N</i>-hexaose Galβ1→3GlcNAcβ1→3 [Galβ1→4GlcNAcβ1→6] Galβ1→4Glc.

Bandara Mithila D MD   Stine Keith J KJ   Demchenko Alexei V AV  

The Journal of organic chemistry 20191205 24


The first synthesis of lacto-<i>N</i>-hexaose (LNH) has been completed using a convergent strategy. The donor-acceptor protecting-leaving group combinations were found to be of paramount significance for achieving successful glycosylations and minimizing side reactions. Lacto-<i>N</i>-tetraose, another common human milk oligosaccharide, was also obtained en route to the target LNH. ...[more]

Similar Datasets

| S-EPMC6897367 | biostudies-literature
| S-EPMC6717531 | biostudies-literature
| S-EPMC7658587 | biostudies-literature
| S-EPMC11370726 | biostudies-literature
| S-EPMC5989456 | biostudies-literature
| S-EPMC5144078 | biostudies-literature
| S-EPMC5502611 | biostudies-literature
| S-EPMC8639736 | biostudies-literature
| S-EPMC5953189 | biostudies-literature
| S-EPMC11600167 | biostudies-literature