Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Tobias-Elias Gloe"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 11, Iss 1, Pp 1096-1104 (2015)
The Amadori rearrangement was employed for the synthesis of C-glycosyl-type D-mannoside analogues, namely 1-propargylamino- and 1-phenylamino-1-deoxy-α-D-manno-heptopyranose. They were investigated as ligands of type 1-fimbriated E. coli bacteria by
Externí odkaz:
https://doaj.org/article/e7ab485f6c034e52b8e1d18c035505a5
Publikováno v:
European Journal of Organic Chemistry. 2018:6971-6982
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6fe09195ace0ec8b1204c5bd8d18054b
https://doi.org/10.1002/ejoc.201801387
https://doi.org/10.1002/ejoc.201801387
Publikováno v:
Carbohydrate Research. 425:1-9
Carbohydrate scaffolds, functionalised according to an AB4-type, were prepared on the basis of α-D-mannopyranosides with various ethyl aglycone moieties, functionalised with 'A'. Four functional groups 'B' were installed at positions 2, 3, 4, and 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b7de6679b7d7d04e900605c8ff5038f
https://doi.org/10.1016/j.carres.2016.02.010
https://doi.org/10.1016/j.carres.2016.02.010
Publikováno v:
European Journal of Organic Chemistry. 2016:4244-4244
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab1f9c1f59a9aafc33a989845de69431
https://doi.org/10.1002/ejoc.201670251
https://doi.org/10.1002/ejoc.201670251