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dc.date.accessioned 2013-09-06T17:02:24Z
dc.date.available 2013-09-06T17:02:24Z
dc.date.issued 1908
dc.identifier.uri http://sedici.unlp.edu.ar/handle/10915/29292
dc.description.abstract 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. en
dc.format.extent 1305-1313 es
dc.language en es
dc.subject Enzimas es
dc.subject Glucosa es
dc.title Studies on enzyme action I en
dc.type Articulo es
sedici.title.subtitle The correlation of the stereoisomeric α- and β-glucosides with the corresponding glucoses en
sedici.creator.person Armstrong, Edward Frankland es
sedici.description.note Material digitalizado en SEDICI en colaboración con la Biblioteca de Física de la Facultad de Ciencias Exactas (UNLP). es
sedici.subject.materias Química es
sedici.description.fulltext true es
mods.originInfo.place Biblioteca del Departamento de Física es
sedici.subtype Articulo es
sedici.rights.license Creative Commons Public Domain Mark (PDM)
sedici.rights.uri http://creativecommons.org/publicdomain/mark/1.0/
sedici.relation.journalTitle Transactions of the Chemical Society es
sedici.relation.journalVolumeAndIssue vol. 88 es


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