4.6 Article

O-Benzoxazolyl imidates as versatile glycosyl donors for chemical glycosylation

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 11, Issue 24, Pages 4068-4076

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c3ob40667a

Keywords

-

Funding

  1. NIGMS [GM077170, GM090254]
  2. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R15GM077170, R01GM090254] Funding Source: NIH RePORTER

Ask authors/readers for more resources

Herein, we report a new class of glycosyl donors, benzoxazolyl imidates, for chemical glycosylation. The O-benzoxazolyl (OBox) leaving group was designed with an aim to compare the relative reactivity and stability of similarly structured S-benzoxazolyl (SBox) glycosides (thioimidates) developed in our lab and glycosyl trichloroacetimidates (TCAI, O-imidates) developed by Schmidt. Novel OBox donors can be activated under catalytic conditions and provided excellent yields in glycosylation. The OBox imidates were found to be more reactive than either SBox or TCAI donors. The high reactivity profile was confirmed in direct competitive experiments and was found beneficial for HPLC-assisted solid-phase synthesis.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available