Zobrazeno 1 - 10
of 66
pro vyhledávání: '"K. F. Stern"'
Autor:
Wu, Kelvin J. Y.1, Tresco, Ben I. C.1, Ramkissoon, Antonio1, Aleksandrova, Elena V.2, Syroegin, Egor A.2, See, Dominic N. Y.1, Liow, Priscilla1, Dittemore, Georgia A.1, Meiyi Yu1, Testolin, Giambattista1, Mitcheltree, Matthew J.1, Liu, Richard Y.1, Svetlov, Maxim S.3,4, Polikanov, Yury S.5,6,7 yuryp@uic.edu, Myers, Andrew G.1 myers@chemistry.harvard.edu
Publikováno v:
Science. 2/16/2024, Vol. 383 Issue 6684, p721-726. 6p. 5 Diagrams.
Publikováno v:
Journal of Medicinal Chemistry. 24:1487-1492
The preparation of 2"-deoxykanamycin B (12) and 2",3',4'-trideoxykanamycin B (14) from neamine (1) is described. Key intermediates in the synthesis of these 2"-deoxyaminoglycoside antibiotics are 3',4'-bis-O-(p-nitrobenzoyl)-1,2',3,6'-tetrakis-N-(tri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbbdc72ce105ad75a8742aaa8acd75b3
https://doi.org/10.1021/jm00144a023
https://doi.org/10.1021/jm00144a023
Publikováno v:
Chemischer Informationsdienst. 13
The preparation of 2"-deoxykanamycin B (12) and 2",3',4'-trideoxykanamycin B (14) from neamine (1) is described. Key intermediates in the synthesis of these 2"-deoxyaminoglycoside antibiotics are 3',4'-bis-O-(p-nitrobenzoyl)-1,2',3,6'-tetrakis-N-(tri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f3f02c28befb7c8ec90f0560f2209e5
https://doi.org/10.1002/chin.198222325
https://doi.org/10.1002/chin.198222325
Publikováno v:
Chemischer Informationsdienst. 15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abd8775b444a63c1496fc4ff3f29d9e8
https://doi.org/10.1002/chin.198431314
https://doi.org/10.1002/chin.198431314
Publikováno v:
Journal of medicinal chemistry. 27(2)
The preparation of a series of analogues of clindamycin is described in which the naturally occurring five-membered cyclic amino acid amide portion of the molecule is replaced by a four-, six-, or seven-membered cyclic amino acid amide. The most inte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f5c8fa70d25066e69894d4fa71d96c40
https://pubmed.ncbi.nlm.nih.gov/6363698
https://pubmed.ncbi.nlm.nih.gov/6363698
Publikováno v:
The American review of respiratory disease. 81
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0f0cb64c0ad2d4c87e4af7af2045e76c
https://pubmed.ncbi.nlm.nih.gov/13829108
https://pubmed.ncbi.nlm.nih.gov/13829108
Autor:
J E, Grady, K F, Stern
Publikováno v:
Antimicrobial agents and chemotherapy. 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9bf04fb34700e9b3e131346772a34fec
https://pubmed.ncbi.nlm.nih.gov/5883427
https://pubmed.ncbi.nlm.nih.gov/5883427
Publikováno v:
American review of tuberculosis. 75(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0762f1596be4c4f873a8d110753d8aef
https://pubmed.ncbi.nlm.nih.gov/13411415
https://pubmed.ncbi.nlm.nih.gov/13411415
Autor:
Walter Morozowich, F. A. Mackellar, K. F. Stern, D.J. Lamb, H. A. Karnes, Englebert L Rowe, C. Lewis
Publikováno v:
Journal of pharmaceutical sciences. 58(12)
Tritylation of 3,4-O-anisylidene lincomycin (II) was found to give 7-O-trityl-3,4-O-anisplidene lincomycin (III), a key intermediate in the synthesis of lincomycin-2-monoesters. The structure of III was established by NMR. Phosphorylation of III with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01e667adf84f55716475d355b71a7af6
https://pubmed.ncbi.nlm.nih.gov/5353265
https://pubmed.ncbi.nlm.nih.gov/5353265