Zobrazeno 1 - 10
of 170
pro vyhledávání: '"D. N. MCGREGOR"'
Autor:
N. H. Andersen, St. F. Brady, C. M. Harris, Th. M. Harris, E. Hecker, K. B. Hindley, D. N. McGregor, J. A. Marshall, J. C. Roberts, R. Schmidt, G. N. Schrauzer, G. A. Swan, Ch. Tamm, H. Wagner, E. Winterfeldt
Mit Beiträgen zahlreicher Fachwissenschaftler
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 263(3)
The in vitro interaction of polyaspartic acid (PAA) with aminoglycosides was evaluated using double diffusion in agar, dialysis chambers and changes in the optical density of test solutions. The results document a reversible, presumably electrostatic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::93742a05644c73f299866c19fa3b85d3
https://pubmed.ncbi.nlm.nih.gov/1469645
https://pubmed.ncbi.nlm.nih.gov/1469645
Publikováno v:
Journal of Medicinal Chemistry. 21:240-242
Hetacillin was oxidized with m-chloroperbenzoic acid to give the corresponding (R)- and (S)-sulfoxides. Ozonization of hetacillin not only oxidized the sulfide but caused unexpected oxidation of the imidazolidine ring to a 2H-imidazoline. The biologi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc55d6550998b1449a126f3964c79aa9
https://doi.org/10.1021/jm00200a022
https://doi.org/10.1021/jm00200a022
Publikováno v:
Chemischer Informationsdienst. 9
Hetacillin was oxidized with m-chloroperbenzoic acid to give the corresponding (R)- and (S)-sulfoxides. Ozonization of hetacillin not only oxidized the sulfide but caused unexpected oxidation of the imidazolidine ring to a 2H-imidazoline. The biologi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68c015de1c0fac9714c007f5d09dcf59
https://doi.org/10.1002/chin.197825304
https://doi.org/10.1002/chin.197825304
Autor:
D N, McGregor
Publikováno v:
Fortschritte der Chemie organischer Naturstoffe = Progress in the chemistry of organic natural products. Progres dans la chimie des substances organiques naturelles. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d6c794bb3c9835bc46236044a2939821
https://pubmed.ncbi.nlm.nih.gov/4372135
https://pubmed.ncbi.nlm.nih.gov/4372135
Publikováno v:
Chemischer Informationsdienst. 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f65116ccbb4585fdd3d1e0b08eaaee05
https://doi.org/10.1002/chin.198222225
https://doi.org/10.1002/chin.198222225
Publikováno v:
Journal of medicinal chemistry. 22(6)
The first reported synthesis of 2-oxocephalosporin derivatives has been achieved via ozonolysis of the corresponding 2-methylenecephalosporins. The new cephalosporin derivatives showed some antibacterial activity against Gram-positive bacteria, but t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f25d0b915d8ae8bdc797d40752de14c9
https://pubmed.ncbi.nlm.nih.gov/458825
https://pubmed.ncbi.nlm.nih.gov/458825
Autor:
D. N. McGregor
Publikováno v:
Fortschritte der Chemie Organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products ISBN: 9783709170960
The purpose of this review is to summarize the important developments in the chemistry of the penicillin molecule which have been reported in the scientific literature during the approximate period 1964 through 1972. The penicillins were intensively
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c220491fbc21c9174aa5f03a42194c9
https://doi.org/10.1007/978-3-7091-7094-6_1
https://doi.org/10.1007/978-3-7091-7094-6_1
Publikováno v:
Chemischer Informationsdienst. 16
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db7e1d633a139f42bd0e6fc5727190fb
https://doi.org/10.1002/chin.198531342
https://doi.org/10.1002/chin.198531342
Autor:
C. U. KIM, D. N. MCGREGOR
Publikováno v:
Chemischer Informationsdienst. 9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e026793d8d39301b63ced8c99e30906
https://doi.org/10.1002/chin.197817335
https://doi.org/10.1002/chin.197817335