Abstract
The first total synthesis of phenylpropanoid glycoside (PhG) isoacteoside 1 is presented. The synthesis employs a novel protection-free strategy leveraging phenylboronic acid as a transient masking agent to enable regioselective mono-rhamnosylation and caffeoylation. This method circumvents the need for traditional multi-step protection and deprotection steps and enhances overall efficiency and yield. Key steps include a one-pot, three-step glycosylation yielding β-D-glucopyranoside, regioselective rhamnosylation via in-situ boronate ester formation, selective caffeoylation at the OH-6 position, and finally one-pot deprotection to furnish isoacteoside in 26% overall yield. This work represents a significant advancement and serves as a model for preparing many PhGs with a sugar residue at OH-2 and an acyl residue at OH-6 of the 2-phenylethyl-β-D-glucoside core. This work sets a viable route for efficient PhG synthesis.
Original language | English |
---|---|
Journal | Chemistry and Biodiversity |
DOIs | |
Publication status | Accepted/In press - 2025 |
Keywords
- boronate ester
- glycosylation
- isoacteoside
- phenylpropanoid glycosides
- transient masking groups