Design and synthesis of multivalent neoglycoconjugates by click conjugations
A highly stereoselective BF3∙OEt2-promoted tandem hydroamination/glycosylation on glycal scaffolds has been developed to form propargyl 3-tosylamino-2,3-dideoxysugars in a one-pot manner. Subsequent construction of multivalent 3-tosylamino-2,3-dideoxyneoglycoconjugates with potential biochemical app...
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sg-ntu-dr.10356-796832023-02-28T19:28:25Z Design and synthesis of multivalent neoglycoconjugates by click conjugations Ding, Feiqing Ji, Li William, Ronny Chai, Hua Liu, Xue-Wei School of Physical and Mathematical Sciences DRNTU::Science::Chemistry::Inorganic chemistry A highly stereoselective BF3∙OEt2-promoted tandem hydroamination/glycosylation on glycal scaffolds has been developed to form propargyl 3-tosylamino-2,3-dideoxysugars in a one-pot manner. Subsequent construction of multivalent 3-tosylamino-2,3-dideoxyneoglycoconjugates with potential biochemical applications was presented herein involving click conjugations as the key reaction step. The copper-catalyzed regioselective click reaction was tremendously accelerated with assistance of microwave irradiation. Published version 2014-08-15T06:15:50Z 2019-12-06T13:30:58Z 2014-08-15T06:15:50Z 2019-12-06T13:30:58Z 2014 2014 Journal Article Ding, F., Ji, L., William, R., Chai, H., & Liu, X.-W. (2014). Design and synthesis of multivalent neoglycoconjugates by click conjugations. Beilstein Journal of Organic Chemistry, 10, 1325-1332. 1860-5397 https://hdl.handle.net/10356/79683 http://hdl.handle.net/10220/20300 10.3762/bjoc.10.134 24991285 en Beilstein journal of organic chemistry © 2014 Ding et al; licensee Beilstein-Institut. This is an Open Access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (http://www.beilstein-journals.org/bjoc) application/pdf |
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DRNTU::Science::Chemistry::Inorganic chemistry Ding, Feiqing Ji, Li William, Ronny Chai, Hua Liu, Xue-Wei Design and synthesis of multivalent neoglycoconjugates by click conjugations |
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A highly stereoselective BF3∙OEt2-promoted tandem hydroamination/glycosylation on glycal scaffolds has been developed to form propargyl 3-tosylamino-2,3-dideoxysugars in a one-pot manner. Subsequent construction of multivalent 3-tosylamino-2,3-dideoxyneoglycoconjugates with potential biochemical applications was presented herein involving click conjugations as the key reaction step. The copper-catalyzed regioselective click reaction was tremendously accelerated with assistance of microwave irradiation. |
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School of Physical and Mathematical Sciences |
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School of Physical and Mathematical Sciences Ding, Feiqing Ji, Li William, Ronny Chai, Hua Liu, Xue-Wei |
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Article |
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Ding, Feiqing Ji, Li William, Ronny Chai, Hua Liu, Xue-Wei |
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Ding, Feiqing |
title |
Design and synthesis of multivalent neoglycoconjugates by click conjugations |
title_short |
Design and synthesis of multivalent neoglycoconjugates by click conjugations |
title_full |
Design and synthesis of multivalent neoglycoconjugates by click conjugations |
title_fullStr |
Design and synthesis of multivalent neoglycoconjugates by click conjugations |
title_full_unstemmed |
Design and synthesis of multivalent neoglycoconjugates by click conjugations |
title_sort |
design and synthesis of multivalent neoglycoconjugates by click conjugations |
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2014 |
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https://hdl.handle.net/10356/79683 http://hdl.handle.net/10220/20300 |
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