Transesterification between acetylated and free carbohydrates

Transesterification reactions have been performed in systems in which both acyl acceptor and acyl donor are carbohydrates with the same skeleton. Basic catalysis proved to be much more efficient than nucleophylic catalysis. Partially acetylated sugar derivatives have been prepared by selective deacy...

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Autores principales: Leit, S., Moradei, O., Du Mortier, C., Fernandez Cirelli, A.
Formato: JOUR
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_03650375_v85_n1-2_p87_Leit
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spelling todo:paper_03650375_v85_n1-2_p87_Leit2023-10-03T15:27:49Z Transesterification between acetylated and free carbohydrates Leit, S. Moradei, O. Du Mortier, C. Fernandez Cirelli, A. Transesterification reactions have been performed in systems in which both acyl acceptor and acyl donor are carbohydrates with the same skeleton. Basic catalysis proved to be much more efficient than nucleophylic catalysis. Partially acetylated sugar derivatives have been prepared by selective deacylation of peracetylated glycosides, using transesterification between a peracetylated sugar and a non-protected carbohydrate. This method compares favourably with known regioselective acylation methods. Fil:Leit, S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Moradei, O. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Fernandez Cirelli, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_03650375_v85_n1-2_p87_Leit
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
description Transesterification reactions have been performed in systems in which both acyl acceptor and acyl donor are carbohydrates with the same skeleton. Basic catalysis proved to be much more efficient than nucleophylic catalysis. Partially acetylated sugar derivatives have been prepared by selective deacylation of peracetylated glycosides, using transesterification between a peracetylated sugar and a non-protected carbohydrate. This method compares favourably with known regioselective acylation methods.
format JOUR
author Leit, S.
Moradei, O.
Du Mortier, C.
Fernandez Cirelli, A.
spellingShingle Leit, S.
Moradei, O.
Du Mortier, C.
Fernandez Cirelli, A.
Transesterification between acetylated and free carbohydrates
author_facet Leit, S.
Moradei, O.
Du Mortier, C.
Fernandez Cirelli, A.
author_sort Leit, S.
title Transesterification between acetylated and free carbohydrates
title_short Transesterification between acetylated and free carbohydrates
title_full Transesterification between acetylated and free carbohydrates
title_fullStr Transesterification between acetylated and free carbohydrates
title_full_unstemmed Transesterification between acetylated and free carbohydrates
title_sort transesterification between acetylated and free carbohydrates
url http://hdl.handle.net/20.500.12110/paper_03650375_v85_n1-2_p87_Leit
work_keys_str_mv AT leits transesterificationbetweenacetylatedandfreecarbohydrates
AT moradeio transesterificationbetweenacetylatedandfreecarbohydrates
AT dumortierc transesterificationbetweenacetylatedandfreecarbohydrates
AT fernandezcirellia transesterificationbetweenacetylatedandfreecarbohydrates
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