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Rapid Synthesis of L-Idosyl Glycosyl Donors from α- Thioglucosides for the Preparation of Heparin Disaccharides

Herczeg, Mihály and Demeter, Fruzsina and Balogh, Tímea and Kelemen, Viktor and Borbás, Anikó (2018) Rapid Synthesis of L-Idosyl Glycosyl Donors from α- Thioglucosides for the Preparation of Heparin Disaccharides. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY (25). pp. 3312-3316. ISSN 1434-193X

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Abstract

A new methodology for the synthesis of the most challenging heparin building block has been developed. Orthogonally protected L-idosyl glycosyl donors were prepared by C5 epimerization of the corresponding thioglucosides using the hydroboration/oxidation method followed by a 4,6-acetal formation. The -anomeric configuration was crucial and the bulky C4 substituent was advantageous for the high L-ido diastereoselectivity. The 4,6-arylmethylene group proved to be a directing element in glycosylation thereby stereoselective -idosylation could be achieved by using idosyl donors without a C-2 participating group.

Item Type: Article
Uncontrolled Keywords: thioglycosides, L-idose, glycosylation, stereoselective, heparin
Subjects: Q Science / természettudomány > QD Chemistry / kémia > QD04 Organic chemistry / szerves kémia
Depositing User: Dr. Mihály Herczeg
Date Deposited: 17 Sep 2018 10:49
Last Modified: 17 Sep 2018 10:49
URI: http://real.mtak.hu/id/eprint/84207

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