Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Reto Hess"'
Publikováno v:
IABSE Symposium, Vancouver 2017: Engineering the Future.
Within the coming decade many ageing rockfall protection galleries in the Swiss Alps will require rehabilitation measures to ensure their durability. Before a gallery is rehabilitated, its current safety level needs to be assessed to decide whether s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::195e764eeaec7a95d038bf78aca55bb4
https://doi.org/10.2749/222137817822208564
https://doi.org/10.2749/222137817822208564
Publikováno v:
IABSE Congress, Stockholm 2016: Challenges in Design and Construction of an Innovative and Sustainable Built Environment.
In order to maintain approximately 1500 engineering structures, the road office of Grisons in Switzerland has to repair or replace between 30 and 50 structures each year. Timing and scope of interventions is mainly driven by the condition state of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce930851070eb570aa3d6bca22f69b2c
https://doi.org/10.2749/stockholm.2016.1472
https://doi.org/10.2749/stockholm.2016.1472
Publikováno v:
Scopus-Elsevier
Catalysis Letters, 92 (3-4)
Catalysis Letters, 92 (3-4)
Catalysis Letters, 92 (3-4)
ISSN:1011-372X
ISSN:1572-879X
ISSN:1011-372X
ISSN:1572-879X
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cddde7e1f1bc52cd31be28df7335f05b
https://doi.org/10.1023/b:catl.0000014336.66209.5a
https://doi.org/10.1023/b:catl.0000014336.66209.5a
Publikováno v:
Tetrahedron: Asymmetry. 15:251-257
Asymmetric hydrogenation of the activated carbonyl group of 1,1,1-trifluoro-2,4-diketones was studied over Pt/Al 2 O 3 modified by various chiral 1,2-aminoalcohols and amines. The best chiral modifiers were cinchonidine and O -methyl-cinchonidine, wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26068a45dfc1df1ae50b9aa58c07fdcf
https://doi.org/10.1016/j.tetasy.2003.10.043
https://doi.org/10.1016/j.tetasy.2003.10.043
Publikováno v:
Journal of Catalysis. 218:453-456
Enantioselective hydrogenation of acetophenone derivatives demonstrates the potential of the Pt–cinchona system in the synthesis of chiral alcohols that possess no functional group in the α-position to the CHOH group. Electron-withdrawing funct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6ac6e30badfe44539a4a0f6cf53ef0e
https://doi.org/10.1016/s0021-9517(02)00179-3
https://doi.org/10.1016/s0021-9517(02)00179-3
Publikováno v:
Journal of Catalysis, Vol. 209, No 2 (2002) pp. 489-500
The relation between the electronic structure of α-substituted ketones and their reactivity in the racemic and enantioselective platinum-catalyzed hydrogenation has been investigated using a combined theoretical and experimental approach. A correlat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bb940cce7b71dcb6bf94fb3294d06fe
https://doi.org/10.1006/jcat.2002.3653
https://doi.org/10.1006/jcat.2002.3653
Publikováno v:
Journal of Catalysis. 186:239-241
Heterogeneous enantioselective hydrogenation of activated ketones in a fixed-bed reactor was achieved by continuous feeding of minute amounts of chiral modifier to the reactant stream. The potential of this concept is illustrated using the hydrogenat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::780e191166e581f1ef35ecffb1efe50f
https://doi.org/10.1006/jcat.1999.2631
https://doi.org/10.1006/jcat.1999.2631
Inversion of enantioselectivity in the platinum-catalyzed hydrogenation of substituted acetophenones
Publikováno v:
Journal of Catalysis, Vol. 222, No 1 (2004) pp. 117-128
The enantioselective hydrogenation of ring-substituted acetophenones that possess no functional group in the α-position to the keto group represents the latest extension of the application range of the Pt–cinchona system. The influence of the type
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cd38cb0ba896364e93fc1e0257bbcd0
https://archive-ouverte.unige.ch/unige:14708
https://archive-ouverte.unige.ch/unige:14708
