Asymmetric synthesis of 1-deoxyazasugars from chiral aziridines†
Abstract
A general and facile synthesis of enantiopure 1-deoxyazasugars was achieved from stereoselective dihydroxylation of a common synthetic intermediate, piperidine ring fused
* Corresponding authors
a
Department of Chemistry and Protein Research Centre for Bio-Industry, Hankuk University of Foreign Studies, Yongin, Korea
E-mail:
hjha@hufs.ac.kr
Fax: +82-31-3304566
Tel: +82-31-3304369
b
Department of Chemistry, Sogang University, Seoul 121-742, Korea
E-mail:
wonkoo@sogang.ac.kr
Fax: +82-2-7010967
Tel: +82-2-7058449
A general and facile synthesis of enantiopure 1-deoxyazasugars was achieved from stereoselective dihydroxylation of a common synthetic intermediate, piperidine ring fused
A. Singh, B. Kim, W. K. Lee and H. Ha, Org. Biomol. Chem., 2011, 9, 1372 DOI: 10.1039/C0OB00730G
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