Abstract
The chemical synthesis of the rare branched human milk oligosaccharide lacto-N-neohexaose (LNnH) was accomplished in total of 19 steps, starting from commercially available disaccharides — lactulose and lactose. The synthesis features regioselective silyl protection using tin chemistry, strategically designed [2+2] and [2+4] glycosylation reactions, and an orthogonal protection/deprotection sequence to ensure efficiency and selectivity. Careful optimization of reaction conditions and donor–acceptor combinations minimized the need for extensive chromatographic purifications, facilitating the isolation of crystalline intermediates in high yields. This streamlined approach provides a scalable and efficient route to LNnH, contributing to the synthetic accessibility of complex human milk oligosaccharides.
Supplementary materials
Title
NMR data
Description
Assignment tables and copies of NMR spectra.
Actions



![Author ORCID: We display the ORCID iD icon alongside authors names on our website to acknowledge that the ORCiD has been authenticated when entered by the user. To view the users ORCiD record click the icon. [opens in a new tab]](https://www.cambridge.org/engage/assets/public/coe/logo/orcid.png)