From conventional to unconventional : glycosylation on semi-protected donors and syntheses towards natural products
The specific stereo-configuration at each anomeric linkage and the diversity in branching burdens the synthesis of glycans. In this thesis, we introduce a widely applicable open-glycosylation method for the boron-assisted construction of various glycosidic connections. Furthermore, we manifested the...
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sg-ntu-dr.10356-1037212023-02-28T23:40:21Z From conventional to unconventional : glycosylation on semi-protected donors and syntheses towards natural products Báti, Gábor Liu Xuewei School of Physical and Mathematical Sciences DRNTU::Science::Chemistry The specific stereo-configuration at each anomeric linkage and the diversity in branching burdens the synthesis of glycans. In this thesis, we introduce a widely applicable open-glycosylation method for the boron-assisted construction of various glycosidic connections. Furthermore, we manifested the practicality of this approach in a one-pot assembly of a model trisaccharide. Lastly, we conceptualized a divergent synthetic route for the syntheses of natural products and made significant steps towards their completion. Doctor of Philosophy 2019-01-09T13:50:10Z 2019-12-06T21:18:47Z 2019-01-09T13:50:10Z 2019-12-06T21:18:47Z 2018 Thesis Báti, G. (2018). From conventional to unconventional : glycosylation on semi-protected donors and syntheses towards natural products. Doctoral thesis, Nanyang Technological University, Singapore. https://hdl.handle.net/10356/103721 http://hdl.handle.net/10220/47430 10.32657/10220/47430 en 131 p. application/pdf |
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DRNTU::Science::Chemistry Báti, Gábor From conventional to unconventional : glycosylation on semi-protected donors and syntheses towards natural products |
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The specific stereo-configuration at each anomeric linkage and the diversity in branching burdens the synthesis of glycans. In this thesis, we introduce a widely applicable open-glycosylation method for the boron-assisted construction of various glycosidic connections. Furthermore, we manifested the practicality of this approach in a one-pot assembly of a model trisaccharide. Lastly, we conceptualized a divergent synthetic route for the syntheses of natural products and made significant steps towards their completion. |
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Liu Xuewei |
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Liu Xuewei Báti, Gábor |
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Theses and Dissertations |
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Báti, Gábor |
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Báti, Gábor |
title |
From conventional to unconventional : glycosylation on semi-protected donors and syntheses towards natural products |
title_short |
From conventional to unconventional : glycosylation on semi-protected donors and syntheses towards natural products |
title_full |
From conventional to unconventional : glycosylation on semi-protected donors and syntheses towards natural products |
title_fullStr |
From conventional to unconventional : glycosylation on semi-protected donors and syntheses towards natural products |
title_full_unstemmed |
From conventional to unconventional : glycosylation on semi-protected donors and syntheses towards natural products |
title_sort |
from conventional to unconventional : glycosylation on semi-protected donors and syntheses towards natural products |
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2019 |
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https://hdl.handle.net/10356/103721 http://hdl.handle.net/10220/47430 |
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