Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Hans Rudolf Pfaendler"'
Publikováno v:
Frontiers in Microbiology, Vol 11 (2020)
ObjectivesTo evaluate the rapid phenotypic CarbaLux test for routine diagnostics in the medical laboratory in a proof of concept study.Methodsisolates of Gram-negative bacteria suspicious for carbapenem resistance including Enterobacterales (67), Pse
Externí odkaz:
https://doaj.org/article/155657019369438a9d52b10171b721ec
Autor:
Gudrun Silvennoinen, Rainer Hartung, Susanne Schlaf, Hans Rudolf Pfaendler, Gregor Golz, Kurt Polborn, Peter Mayer
Publikováno v:
Synthesis. 2009:495-501
New formaldehyde derivatives were prepared in good yields by a short and versatile route. Several crystal structures of corresponding thioacetic acid esters and thiols were determined. The thioacetates were cleaved under acidic or basic conditions af
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76f65e3a5b534526558e7f3c203cd814
https://doi.org/10.1055/s-0028-1083305
https://doi.org/10.1055/s-0028-1083305
Publikováno v:
Helvetica Chimica Acta. 88:1486-1490
The present publication describes an efficient and mild three-step conversion of a terminal olefin 1 into the corresponding 1,2-diamine 5. The sequence includes: azidoiodination, substitution with NaN3, and catalytic hydrogenolysis. The terminal 1,2-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86ab7b592ad65a9400f2a140a88735ed
https://doi.org/10.1002/hlca.200590119
https://doi.org/10.1002/hlca.200590119
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 7:2217-2222
The first stable penem sulfoxides 4a, 4b and the novel penem sulfone 6b were prepared. The rates of hydrolysis and the biological activities were examined.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c985bfe4634603f50b4c799e795b6c79
https://doi.org/10.1016/s0960-894x(97)00401-0
https://doi.org/10.1016/s0960-894x(97)00401-0
Autor:
Hans Rudolf Pfaendler, Claus Medicus
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 7:623-628
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89f8810782b8ec5c808bc89891f13f03
https://doi.org/10.1016/s0960-894x(97)00070-x
https://doi.org/10.1016/s0960-894x(97)00070-x
Autor:
Volker Weimar, Hans Rudolf Pfaendler
Publikováno v:
Synthesis. 1996:1345-1349
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6555851bc5e206c8cbd82c3606674bc9
https://doi.org/10.1055/s-1996-4390
https://doi.org/10.1055/s-1996-4390
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 3:2211-2218
As with the oxapenems, the 2-tert-butyl substituents substantially increased the hydrolytic stability of penems. The corresponding penems 1 and 2 were prepared and found to be extremely stable compounds. 2 showed good in vitro activity against gram-p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d514fa262f7da8c5f0942ead241e94d
https://doi.org/10.1016/s0960-894x(01)80927-6
https://doi.org/10.1016/s0960-894x(01)80927-6
Autor:
Hans Rudolf Pfaendler, Frank Weisner
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16abbb199d8c4c40dbb63b9aa5b4bc8f
https://doi.org/10.1002/chin.199529213
https://doi.org/10.1002/chin.199529213
Autor:
Volker Weimar, Hans Rudolf Pfaendler
Publikováno v:
ChemInform. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13caec92cb2f59df630d6e50d63cfad1
https://doi.org/10.1002/chin.199715214
https://doi.org/10.1002/chin.199715214
Publikováno v:
ChemInform. 28
The first stable penem sulfoxides 4a, 4b and the novel penem sulfone 6b were prepared. The rates of hydrolysis and the biological activities were examined.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c6a8f153fd2bac00bab070efd70cff6
https://doi.org/10.1002/chin.199752257
https://doi.org/10.1002/chin.199752257