Zobrazeno 1 - 10
of 22
pro vyhledávání: '"John H. C. Nayler"'
Autor:
W. J. Iii Smith, J. W. Tyler, K. A. Ashline, J. P. Clayton, Jeremy R. Everett, M. Sabat, E. A. Cutmore, R. P. Attrill, John H. C. Nayler, M. L. Vieira, E. K. Chess, David E. Pereira
Publikováno v:
ChemInform. 21
Autor:
Walter J. Smith, Edward K. Chess, Michael L. Vieira, Michal Sabat, Robin P. Attrill, John H. C. Nayler, Kirk A. Ashline, Jeremy R. Everett, David E. Pereira, J. Peter Clayton, Ernest A. Cutmore, John W. Tyler
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2. :1559
High-field nuclear magnetic resonance spectroscopy, mass spectrometry, infrared spectroscopy, and ultraviolet spectroscopy were used to determine the structures of two novel degradation productions of the penicillins sodium nafcillin (1) and sodium o
Autor:
John H. C. Nayler
Publikováno v:
Journal of Antimicrobial Chemotherapy. 19:713-732
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :22-25
The action of methyl iodide and strong anhydrous base on methyl penicillanate or its 6α-bromo-derivative leads to S-methylation and cleavage of both thiazolidine and β-lactam rings, but with methyl 6,6-dibromopenicillanate the β-lactam system rema
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
Publikováno v:
Chemischer Informationsdienst. 5
Publikováno v:
Chemischer Informationsdienst. 7
Publikováno v:
Chemischer Informationsdienst. 9
The vital role of D-alanine and L-lysine in the peptidoglycan crosslinking process in the bacterial cell wall prompted preparation of various small peptides incorporating these amino acids. N-Iodoacetyl or -bromoacetyl derivatives of the peptides wer
Publikováno v:
Chemischer Informationsdienst. 6
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