Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Sandra Bochmann"'
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
Publikováno v:
Tetrahedron Letters. 54:6185-6188
Three different reports on the syntheses of isolable 1H-azirines 6, 15, and 21 were reinvestigated. Instead of the claimed heterocyclic product 6, the isomeric thiazole derivative 7 has been isolated now with nearly identical yield. In the case of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9db969a62ebd1cbae4442c9827a45305
https://doi.org/10.1016/j.tetlet.2013.08.122
https://doi.org/10.1016/j.tetlet.2013.08.122
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