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
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/29292
Ver los metadatos del registro completo
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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 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Articulo http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://sedici.unlp.edu.ar/handle/10915/29292 |
url |
http://sedici.unlp.edu.ar/handle/10915/29292 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess http://creativecommons.org/publicdomain/mark/1.0/ Creative Commons Public Domain Mark (PDM) |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://creativecommons.org/publicdomain/mark/1.0/ Creative Commons Public Domain Mark (PDM) |
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application/pdf 1305-1313 |
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SEDICI (UNLP) - Universidad Nacional de La Plata |
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