TY  - CHAP
A1  - Juchler, Ingo
T1  - „…die im Dunkeln sieht man nicht“
BT  - zur Mensch-Tier-Beziehung in der politischen Bildung
T2  - Standortbestimmung Politische Bildung
Y1  - 2022
SN  - 978-3-7344-1352-0
SN  - 978-3-7344-1353-7
U6  - https://doi.org/10.46499/1900
SP  - 163
EP  - 175
PB  - Wochenschau Wissenschaft
CY  - Frankfurt am Main
ER  - 
TY  - BOOK
A1  - Kroener, Bernhard R.
T1  - „…weshalb kämpft ihr mit ihnen …“ : Kameradschaftserfahrungen und Emanzipationsbestrebungen deutscher und österreichisch-ungarischer Soldaten jüdischer Herkunft 1866–1918
N2  - Der vorliegende Text beschäftigt sich mit der religiös, kulturell und rassisch begründeten Ausgrenzung von Minderheiten durch die Mehrheitsgesellschaft im Zeitalter der europäischen Nationalstaaten, die fast immer im Rückgriff auf konstruierte historische Belege geschieht. Am Beispiel von Deutschland und Österreich wird der Zusammenhang aufgezeigt zwischen der staatsbürgerlichen Gleichstellung der Juden im 19. und frühen 20. Jahrhundert einerseits, und Krieg und Nationsbildung, bürgerlichem Selbstverständnis und Geschichtsdeutung in legitimatorischer Absicht andererseits.
N2  - The present text is dealing with the exclusion of minorities by the majority of a population in the era of nation building and nationalism, which is justified by a religious, cultural and racial otherness, very often proved by construed historical evidence. While comparing the situation in Germany and Austria the author shows the interrelation between the emancipation of the Jews in the 19th. and early 20th. century on one hand and war and nation building, self conception of the bourgeoisie and their interpretation of history on the other.
KW  - Emanzipation der Juden
KW  - Jüdische Soldaten
KW  - Krieg
KW  - Nationalismus
KW  - Antisemitismus
KW  - Emancipation of the Jews
KW  - Jewish soldiers
KW  - war
KW  - nationalism
KW  - antisemitism
Y1  - 2007
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus-15578
SN  - 978-3-939469-98-8
ER  - 
TY  - GEN
A1  - Jacobi, Juliane
T1  - ›Mütterlichkeit‹ und ›natürliche‹ Begabung zur Erziehung : Lehrerinnen in der bürgerlichen Gesellschaft
N2  - Inhalt: 1.1. Veröffentlichte Intimität 1.2. Von der ›Bestimmung des Weibes zur höheren Geistesbildung‹ zur ›Sogenannten Emancipation‹ 2. Der allgemeine deutsche Lahrerinnenverein (ADLV) und seine Professionalisierungsstrategie 3. Vom Fortschritt und seinen Kosten
T3  - Zweitveröffentlichungen der Universität Potsdam : Humanwissenschaftliche Reihe - paper 217 
Y1  - 1989
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus-47751
ER  - 
TY  - JOUR
A1  - Wang, Xuebin
A1  - Wang, Xiaoli
A1  - Hu, Jing
A1  - Wang, Zhaoya
A1  - Pimpalpalle, Tukaram M.
A1  - Linker, Torsten
A1  - Yin, Jian
T1  - Study on the Synthesis of Novel Sugar Amino Acids
T1  - 新型糖氨基酸类化合物的合成研究
JF  - Acta chimica Sinica = Huaxue-xuebao
N2  - Sugar amino acids (SAAs) are carbohydrate derivatives bearing both amino and carboxylic acid functional groups. SAAs represent an important class of multifunctional building blocks, which are amenable to serve as glycomimetics or peptidomimetics with well-defined structures and useful properties. Because SAAs exist in nature in many forms with various biological activities, recently, many unnatural SAAs, as the demand for finding new molecules to discover new drugs and new materials, have been designed and synthesized by a number of research groups. In this paper, we have developed a convenient method for the synthesis of novel SAAs gluco-7 and galacto-7 for the first time. The structure of gluco-7 was similar to the natural SAA glucosaminuronic acid that was a component of many typical bacterial cell walls and could be used for the preparation of type D flu vaccine; while galacto-7 was similar to the natural SAA galactosaminuronic acid that was one of bacterial Vi-antigen components of Escherichia coli. Starting from unexpensive and commercially available 3,4,6-tri-O-acetyl-D-glucal and 3,4,6-tri-O-acetyl-D-galactal, two novel SAAs gluco-7 and galacto-7 were achieved in the linear 6 steps with 34% overall yield and 19% overall yield, respectively. The key reactions included radical addition, decarboxylation, iodine generation reaction, azide reaction and reductive amination reaction. The crucial step was the synthesis of the target compound gluco-7 from gluco-6. By using method A, the target compound gluco-7 was obtained in 4 steps with 63% overall yield. To optimize the transformation from gluco-6 to gluco-7, method B was developed to generate gluco-7 by using one-pot reaction successfully with 76% yield only in one step. It proved that method B was superior to method A with shorter steps and higher yields. All the new compounds were characterized by IR, H-1 NMR, C-13 NMR and HRMS data. Study on the synthesis and biological evaluation of linear and cyclic oligomers derived from gluco-7 and galacto-7 are currently in progress.
KW  - sugar amino acids
KW  - glycal
KW  - radical addition
KW  - one-pot reaction
KW  - synthesis
Y1  - 2015
U6  - https://doi.org/10.6023/A15030205
SN  - 0567-7351
VL  - 73
IS  - 7
SP  - 699
EP  - 704
PB  - Science China Press
CY  - Beijing
ER  -