Benzoyl derivatives of d-gluconolactones and their reaction with alcohols
Benzoylation of d-glucono-1,4-lactone and d-glucono-1,5-lactone afforded the corresponding tetra-O-benzoyl derivatives. They showed the optical rotation and i.r. spectral absorption characteristic for 1,4 or 1,5-lactones, respectively. Opening of the lactone ring was effected by treatment with alcoh...
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1970
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paper:paper_00086215_v13_n1_p9_deLederkremer2023-06-08T14:32:14Z Benzoyl derivatives of d-gluconolactones and their reaction with alcohols Muchnik de Lederkremer, Rosa María Fernández Cirelli, Alicia Deferrari, Jorge O. Benzoylation of d-glucono-1,4-lactone and d-glucono-1,5-lactone afforded the corresponding tetra-O-benzoyl derivatives. They showed the optical rotation and i.r. spectral absorption characteristic for 1,4 or 1,5-lactones, respectively. Opening of the lactone ring was effected by treatment with alcohols to give tetra-O-benzoyl-d-gluconates having an unesterified hydroxyl group at C-4 or C-5, respectively. © 1970. Fil:de Lederkremer, R.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Fernández Cirelli, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Deferrari, J.O. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 1970 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00086215_v13_n1_p9_deLederkremer http://hdl.handle.net/20.500.12110/paper_00086215_v13_n1_p9_deLederkremer |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
description |
Benzoylation of d-glucono-1,4-lactone and d-glucono-1,5-lactone afforded the corresponding tetra-O-benzoyl derivatives. They showed the optical rotation and i.r. spectral absorption characteristic for 1,4 or 1,5-lactones, respectively. Opening of the lactone ring was effected by treatment with alcohols to give tetra-O-benzoyl-d-gluconates having an unesterified hydroxyl group at C-4 or C-5, respectively. © 1970. |
author |
Muchnik de Lederkremer, Rosa María Fernández Cirelli, Alicia Deferrari, Jorge O. |
spellingShingle |
Muchnik de Lederkremer, Rosa María Fernández Cirelli, Alicia Deferrari, Jorge O. Benzoyl derivatives of d-gluconolactones and their reaction with alcohols |
author_facet |
Muchnik de Lederkremer, Rosa María Fernández Cirelli, Alicia Deferrari, Jorge O. |
author_sort |
Muchnik de Lederkremer, Rosa María |
title |
Benzoyl derivatives of d-gluconolactones and their reaction with alcohols |
title_short |
Benzoyl derivatives of d-gluconolactones and their reaction with alcohols |
title_full |
Benzoyl derivatives of d-gluconolactones and their reaction with alcohols |
title_fullStr |
Benzoyl derivatives of d-gluconolactones and their reaction with alcohols |
title_full_unstemmed |
Benzoyl derivatives of d-gluconolactones and their reaction with alcohols |
title_sort |
benzoyl derivatives of d-gluconolactones and their reaction with alcohols |
publishDate |
1970 |
url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00086215_v13_n1_p9_deLederkremer http://hdl.handle.net/20.500.12110/paper_00086215_v13_n1_p9_deLederkremer |
work_keys_str_mv |
AT muchnikdelederkremerrosamaria benzoylderivativesofdgluconolactonesandtheirreactionwithalcohols AT fernandezcirellialicia benzoylderivativesofdgluconolactonesandtheirreactionwithalcohols AT deferrarijorgeo benzoylderivativesofdgluconolactonesandtheirreactionwithalcohols |
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1768543827270828032 |