Studies on enzyme action I : The correlation of the stereoisomeric α- and β-glucosides with the corresponding glucoses

Autores
Armstrong, Edward Frankland
Año de publicación
1908
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Of the explanations put forward of the change in rotatory power which glucose undergoes in solution— a phenomenon discovered by Dubrunfaut in 1846— the most probable is that suggested by Lowry (Trans., 1899, 75, 213), which connects the change of rotatory power of glucose with a reversible isomeric change. When this explanation was first given, it was not possible to decide definitely what formulae were to be assigned to the dynamic isomerides. In view, however, of observations made during the investigation of various glucoside derivatives (Fischer and Armstrong, Ber., 1901, 34, 2885; 1902, 35, 833, 3144 and 3153), in the course of which the existence of two un­ doubtedly stereoisomerie series of glucose derivatives was discovered and their relationship to the α- and β-methylglucosides established, it now seems probable that a lactonic structure may be assigned to the isomeric glucoses: these isomerides are, in fact, the two possible stereoisomeric lactones.
Material digitalizado en SEDICI en colaboración con la Biblioteca de Física de la Facultad de Ciencias Exactas (UNLP).
Biblioteca del Departamento de Física
Materia
Química
Enzimas
Glucosa
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/publicdomain/mark/1.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/29292

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network_name_str SEDICI (UNLP)
spelling Studies on enzyme action I : The correlation of the stereoisomeric α- and β-glucosides with the corresponding glucosesArmstrong, Edward FranklandQuímicaEnzimasGlucosaOf the explanations put forward of the change in rotatory power which glucose undergoes in solution— a phenomenon discovered by Dubrunfaut in 1846— the most probable is that suggested by Lowry (Trans., 1899, 75, 213), which connects the change of rotatory power of glucose with a reversible isomeric change. When this explanation was first given, it was not possible to decide definitely what formulae were to be assigned to the dynamic isomerides. In view, however, of observations made during the investigation of various glucoside derivatives (Fischer and Armstrong, Ber., 1901, 34, 2885; 1902, 35, 833, 3144 and 3153), in the course of which the existence of two un­ doubtedly stereoisomerie series of glucose derivatives was discovered and their relationship to the α- and β-methylglucosides established, it now seems probable that a lactonic structure may be assigned to the isomeric glucoses: these isomerides are, in fact, the two possible stereoisomeric lactones.Material digitalizado en SEDICI en colaboración con la Biblioteca de Física de la Facultad de Ciencias Exactas (UNLP).Biblioteca del Departamento de Física1908info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf1305-1313http://sedici.unlp.edu.ar/handle/10915/29292enginfo:eu-repo/semantics/openAccesshttp://creativecommons.org/publicdomain/mark/1.0/Creative Commons Public Domain Mark (PDM)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-29T10:57:17Zoai:sedici.unlp.edu.ar:10915/29292Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 10:57:18.18SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Studies on enzyme action I : The correlation of the stereoisomeric α- and β-glucosides with the corresponding glucoses
title Studies on enzyme action I : The correlation of the stereoisomeric α- and β-glucosides with the corresponding glucoses
spellingShingle Studies on enzyme action I : The correlation of the stereoisomeric α- and β-glucosides with the corresponding glucoses
Armstrong, Edward Frankland
Química
Enzimas
Glucosa
title_short Studies on enzyme action I : The correlation of the stereoisomeric α- and β-glucosides with the corresponding glucoses
title_full Studies on enzyme action I : The correlation of the stereoisomeric α- and β-glucosides with the corresponding glucoses
title_fullStr Studies on enzyme action I : The correlation of the stereoisomeric α- and β-glucosides with the corresponding glucoses
title_full_unstemmed Studies on enzyme action I : The correlation of the stereoisomeric α- and β-glucosides with the corresponding glucoses
title_sort Studies on enzyme action I : The correlation of the stereoisomeric α- and β-glucosides with the corresponding glucoses
dc.creator.none.fl_str_mv Armstrong, Edward Frankland
author Armstrong, Edward Frankland
author_facet Armstrong, Edward Frankland
author_role author
dc.subject.none.fl_str_mv Química
Enzimas
Glucosa
topic Química
Enzimas
Glucosa
dc.description.none.fl_txt_mv Of the explanations put forward of the change in rotatory power which glucose undergoes in solution— a phenomenon discovered by Dubrunfaut in 1846— the most probable is that suggested by Lowry (Trans., 1899, 75, 213), which connects the change of rotatory power of glucose with a reversible isomeric change. When this explanation was first given, it was not possible to decide definitely what formulae were to be assigned to the dynamic isomerides. In view, however, of observations made during the investigation of various glucoside derivatives (Fischer and Armstrong, Ber., 1901, 34, 2885; 1902, 35, 833, 3144 and 3153), in the course of which the existence of two un­ doubtedly stereoisomerie series of glucose derivatives was discovered and their relationship to the α- and β-methylglucosides established, it now seems probable that a lactonic structure may be assigned to the isomeric glucoses: these isomerides are, in fact, the two possible stereoisomeric lactones.
Material digitalizado en SEDICI en colaboración con la Biblioteca de Física de la Facultad de Ciencias Exactas (UNLP).
Biblioteca del Departamento de Física
description Of the explanations put forward of the change in rotatory power which glucose undergoes in solution— a phenomenon discovered by Dubrunfaut in 1846— the most probable is that suggested by Lowry (Trans., 1899, 75, 213), which connects the change of rotatory power of glucose with a reversible isomeric change. When this explanation was first given, it was not possible to decide definitely what formulae were to be assigned to the dynamic isomerides. In view, however, of observations made during the investigation of various glucoside derivatives (Fischer and Armstrong, Ber., 1901, 34, 2885; 1902, 35, 833, 3144 and 3153), in the course of which the existence of two un­ doubtedly stereoisomerie series of glucose derivatives was discovered and their relationship to the α- and β-methylglucosides established, it now seems probable that a lactonic structure may be assigned to the isomeric glucoses: these isomerides are, in fact, the two possible stereoisomeric lactones.
publishDate 1908
dc.date.none.fl_str_mv 1908
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dc.language.none.fl_str_mv eng
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dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
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Creative Commons Public Domain Mark (PDM)
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Creative Commons Public Domain Mark (PDM)
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1305-1313
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