Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Oliver Plefka"'
Autor:
Klaus Banert, Sandra Bochmann, Andreas Ihle, Oliver Plefka, Florian Taubert, Tina Walther, Marcus Korb, Tobias Rüffer, Heinrich Lang
Publikováno v:
Molecules, Vol 19, Iss 9, Pp 14022-14035 (2014)
Cyclooctyne and cycloocten-5-yne undergo, at room temperature, a 1,3-dipolar cycloaddition with dialkyl acetylenedicarboxylates 1a,b to generate furan-derived short-lived intermediates 2, which can be trapped by two additional equivalents of 1a,b or
Externí odkaz:
https://doaj.org/article/2ef964634ce94571862febc7553e9aa5
Autor:
Klaus Banert, Oliver Plefka
Publikováno v:
Angewandte Chemie International Edition. 50:6171-6174
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6862dbad145cfdf64c031a7c9e76f211
https://doi.org/10.1002/anie.201101326
https://doi.org/10.1002/anie.201101326
Autor:
Klaus Banert, Oliver Plefka
Publikováno v:
Angewandte Chemie. 123:6295-6298
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf5315260bfa84b151a5b810b6f5d2db
https://doi.org/10.1002/ange.201101326
https://doi.org/10.1002/ange.201101326
Autor:
Gertrud Auer, Oliver Plefka, Betül Karatas, Christian Mück-Lichtenfeld, Stefan Grimme, Sebastian Rendler, Martin Oestreich, Roland Fröhlich
Publikováno v:
Chemistry - A European Journal. 14:11512-11528
Ligand-stabilized copper(I)- hydride catalyzes the dehydrogenative Si-O coupling of alcohols and silanes— a process that was found to proceed without racemization at the silicon atom if asymmetrically substituted. The present investigation starts f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b35efb514db7cf6cadd115b2d756366b
https://doi.org/10.1002/chem.200801377
https://doi.org/10.1002/chem.200801377
Autor:
Lang, Klaus Banert, Sandra Bochmann, Andreas Ihle, Oliver Plefka, Florian Taubert, Tina Walther, Marcus Korb, Tobias Rüffer, Heinrich
Publikováno v:
Molecules; Volume 19; Issue 9; Pages: 14022-14035
Cyclooctyne and cycloocten-5-yne undergo, at room temperature, a 1,3-dipolar cycloaddition with dialkyl acetylenedicarboxylates 1a,b to generate furan-derived short-lived intermediates 2, which can be trapped by two additional equivalents of 1a,b or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::27af969ce2081033fe14b56d05ecf831