Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Patricia Tolliday"'
Autor:
A. J. Eglington, Michael J. Pearson, Patricia Tolliday, R. Sutherland, Robert Southgate, Terence C. Smale, E. G. Brain, John H. C. Nayler, M. J. Basker, N. F. Osborne
Publikováno v:
Chemischer Informationsdienst. 8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d62cbf1b0e0277b3c3a00e5e887dff0
https://doi.org/10.1002/chin.197749388
https://doi.org/10.1002/chin.197749388
Publikováno v:
Chemischer Informationsdienst. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fe59677ad49d0ef3dd28c8684af4bb2
https://doi.org/10.1002/chin.197524461
https://doi.org/10.1002/chin.197524461
Autor:
R. Sutherland, M. J. Basker, Robert Southgate, Michael J. Pearson, Terence C. Smale, Patricia Tolliday, John H. C. Nayler, Edward G. Brain, Neal F. Osborne, A. J. Eglington
Publikováno v:
Journal of medicinal chemistry. 20(8)
tert-Butyl 7beta-aminoceph-3-em-4-carboxylates carrying either benzyl or 3-pyridylmethyl substituents at position 3 have been prepared by a multistep modification of the penicillin nucleus. Acylation of either amine, followed by deprotection, gave a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea43a247f56a9e0031467a0a576b26b7
https://pubmed.ncbi.nlm.nih.gov/894679
https://pubmed.ncbi.nlm.nih.gov/894679
Autor:
E. G. Brain, Terence C. Smale, L. W. Mizen, R. Sutherland, N. F. Osborne, Michael J. Pearson, Patricia Tolliday, John H. C. Nayler, B. G. James, A. J. Eglington, Robert Southgate, M. J. Basker
Publikováno v:
Chemischer Informationsdienst. 8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ccbf2231a560def3fcaa12e10e231c7
https://doi.org/10.1002/chin.197749385
https://doi.org/10.1002/chin.197749385
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb0026521a8712986505405ba8764122
https://doi.org/10.1002/chin.197137405
https://doi.org/10.1002/chin.197137405
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :562
Treatment of 6β-(triphenylmethylamino)penicillanates with certain alkylating agents in the presence of strong anhydrous bases causes S-alkylation and cleavage of the thiazolidine ring between the sulphur atom and C-2. The scope and possible mechanis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23b4f4a5279095a44c228a1465843590
https://doi.org/10.1039/p19750000562
https://doi.org/10.1039/p19750000562
Autor:
A. John Eglington, Edward G. Brain, John H. C. Nayler, Robert Southgate, Neal F. Osborne, Patricia Tolliday
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :2479
6-Acylaminopenam-3-carboxylic esters substituted at C-2 by one or two alkoxycarbonyl groups or by an acetyl group have been prepared from penicillins. The azetidinone ring remained intact throughout the reaction sequence, and the thiazolidine ring wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4ebc372ff8172e6f82193bcce0bd8f0
https://doi.org/10.1039/p19770002479
https://doi.org/10.1039/p19770002479
Publikováno v:
Journal of the Chemical Society D: Chemical Communications. :590
Treatment of p-methoxybenzyl 6β-(triphenylmethylamino)penicillanate (Ia) with methyl iodide and strong anhydrous base caused selective cleavage of the thiazolidine ring to give 1-(1-p-methoxybenzyloxycarbonyl-2-methylprop-1-enyl)-4R-methylthio-3R-(t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32a70ee80e3205b24121fba65d70ed88
https://doi.org/10.1039/c29710000590
https://doi.org/10.1039/c29710000590