Electrochemical glycosylation in the presence of a catalytic chemical mediator
Electrochemical glycosylation of thioglycoside donors proceeds efficiently in an undivided cell in the presence of a catalytic amount of the chemical mediator (4-bromophenyl) ammoniumyl hexachloroantimonate (BAHA). In comparison with electrochemical glycosylation alone, the use of a catalytic amount...
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Format: | Journal article |
Language: | English |
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2008
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_version_ | 1797092481570963456 |
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author | Drouin, L Compton, R Fairbanks, A |
author_facet | Drouin, L Compton, R Fairbanks, A |
author_sort | Drouin, L |
collection | OXFORD |
description | Electrochemical glycosylation of thioglycoside donors proceeds efficiently in an undivided cell in the presence of a catalytic amount of the chemical mediator (4-bromophenyl) ammoniumyl hexachloroantimonate (BAHA). In comparison with electrochemical glycosylation alone, the use of a catalytic amount of BAHA greatly increases the rate of reaction, reduces the potential required and inhibits ester-protecting group migrations. Copyright © 2008 John Wiley and Sons, Ltd. |
first_indexed | 2024-03-07T03:46:31Z |
format | Journal article |
id | oxford-uuid:bfa9a3a6-fdd5-4166-a26a-4baf49efa050 |
institution | University of Oxford |
language | English |
last_indexed | 2024-03-07T03:46:31Z |
publishDate | 2008 |
record_format | dspace |
spelling | oxford-uuid:bfa9a3a6-fdd5-4166-a26a-4baf49efa0502022-03-27T05:49:05ZElectrochemical glycosylation in the presence of a catalytic chemical mediatorJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:bfa9a3a6-fdd5-4166-a26a-4baf49efa050EnglishSymplectic Elements at Oxford2008Drouin, LCompton, RFairbanks, AElectrochemical glycosylation of thioglycoside donors proceeds efficiently in an undivided cell in the presence of a catalytic amount of the chemical mediator (4-bromophenyl) ammoniumyl hexachloroantimonate (BAHA). In comparison with electrochemical glycosylation alone, the use of a catalytic amount of BAHA greatly increases the rate of reaction, reduces the potential required and inhibits ester-protecting group migrations. Copyright © 2008 John Wiley and Sons, Ltd. |
spellingShingle | Drouin, L Compton, R Fairbanks, A Electrochemical glycosylation in the presence of a catalytic chemical mediator |
title | Electrochemical glycosylation in the presence of a catalytic chemical mediator |
title_full | Electrochemical glycosylation in the presence of a catalytic chemical mediator |
title_fullStr | Electrochemical glycosylation in the presence of a catalytic chemical mediator |
title_full_unstemmed | Electrochemical glycosylation in the presence of a catalytic chemical mediator |
title_short | Electrochemical glycosylation in the presence of a catalytic chemical mediator |
title_sort | electrochemical glycosylation in the presence of a catalytic chemical mediator |
work_keys_str_mv | AT drouinl electrochemicalglycosylationinthepresenceofacatalyticchemicalmediator AT comptonr electrochemicalglycosylationinthepresenceofacatalyticchemicalmediator AT fairbanksa electrochemicalglycosylationinthepresenceofacatalyticchemicalmediator |