Preparation of D-glucose dibenzamide from pentabenzoyl-D-α-glucose [19]
THE usual reaction product of the treatment of the acylated nitriles of aldonic acids with ammonia are the aldose diacetamides1. A variation of this reaction was found when Hockett and Chandler2, by treating hexa-acetyl-D-α-glucoheptonic acid nitrile with ammonia, obtained N-acetyl-D-glucofuranosyla...
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paper:paper_00280836_v167_n4236_p42_Deulofeu2023-06-08T14:54:39Z Preparation of D-glucose dibenzamide from pentabenzoyl-D-α-glucose [19] Deulofeu, Venancio Deferrari, Jorge O. glucose article GLUCOSE Glucose THE usual reaction product of the treatment of the acylated nitriles of aldonic acids with ammonia are the aldose diacetamides1. A variation of this reaction was found when Hockett and Chandler2, by treating hexa-acetyl-D-α-glucoheptonic acid nitrile with ammonia, obtained N-acetyl-D-glucofuranosylamine. The same product resulted from the action of ammonia on penta-acetyl-aldehydo-D-glucose. Later, Niemann and Hays3 prepared N-acetyl-D-glucofuranosylamine by the action of methanolic ammonia on penta-acetyl-D-β-glucose, a reaction that produced the transformation of the original pyranose ring of the acetylated glucose into a furanose structure. © 1951 Nature Publishing Group. Fil:Deulofeu, V. 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. 1951 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00280836_v167_n4236_p42_Deulofeu http://hdl.handle.net/20.500.12110/paper_00280836_v167_n4236_p42_Deulofeu |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
glucose article GLUCOSE Glucose |
spellingShingle |
glucose article GLUCOSE Glucose Deulofeu, Venancio Deferrari, Jorge O. Preparation of D-glucose dibenzamide from pentabenzoyl-D-α-glucose [19] |
topic_facet |
glucose article GLUCOSE Glucose |
description |
THE usual reaction product of the treatment of the acylated nitriles of aldonic acids with ammonia are the aldose diacetamides1. A variation of this reaction was found when Hockett and Chandler2, by treating hexa-acetyl-D-α-glucoheptonic acid nitrile with ammonia, obtained N-acetyl-D-glucofuranosylamine. The same product resulted from the action of ammonia on penta-acetyl-aldehydo-D-glucose. Later, Niemann and Hays3 prepared N-acetyl-D-glucofuranosylamine by the action of methanolic ammonia on penta-acetyl-D-β-glucose, a reaction that produced the transformation of the original pyranose ring of the acetylated glucose into a furanose structure. © 1951 Nature Publishing Group. |
author |
Deulofeu, Venancio Deferrari, Jorge O. |
author_facet |
Deulofeu, Venancio Deferrari, Jorge O. |
author_sort |
Deulofeu, Venancio |
title |
Preparation of D-glucose dibenzamide from pentabenzoyl-D-α-glucose [19] |
title_short |
Preparation of D-glucose dibenzamide from pentabenzoyl-D-α-glucose [19] |
title_full |
Preparation of D-glucose dibenzamide from pentabenzoyl-D-α-glucose [19] |
title_fullStr |
Preparation of D-glucose dibenzamide from pentabenzoyl-D-α-glucose [19] |
title_full_unstemmed |
Preparation of D-glucose dibenzamide from pentabenzoyl-D-α-glucose [19] |
title_sort |
preparation of d-glucose dibenzamide from pentabenzoyl-d-α-glucose [19] |
publishDate |
1951 |
url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00280836_v167_n4236_p42_Deulofeu http://hdl.handle.net/20.500.12110/paper_00280836_v167_n4236_p42_Deulofeu |
work_keys_str_mv |
AT deulofeuvenancio preparationofdglucosedibenzamidefrompentabenzoyldaglucose19 AT deferrarijorgeo preparationofdglucosedibenzamidefrompentabenzoyldaglucose19 |
_version_ |
1768545273159614464 |