Journal
ORGANIC LETTERS
Volume 15, Issue 15, Pages 3974-3977Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol401755e
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Funding
- NSFC [21172156, 21021001]
- 973 program [2010CB833202]
- Ministry of Education [NCET-08-0377, 20100181110082]
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A new beta-stereoselective D- and L-arabinofuranosylation method has been developed employing 5-O-(2-quinolinecarbonyl) substituted arabinosyl ethyl thioglycosides as glycosyl donors. The approach allows a wide range of acceptor substrates to be used; the beta-selectivity is good-to-excellent. Stereoselective synthesis of a mannose-capped octasaccharide portion from a mycobacterial cell wall polysaccharide was then carried out to demonstrate the utility of this methodology.
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