Search Results - Eglington, AJ

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  1. 1
    Novel C-2 substituted carbapenem derivatives. Part III. Synthesis and biological activity of 2-(functionalised ethenyl, oxyiminomethyl and alpha

    Novel C-2 substituted carbapenem derivatives. Part III. Synthesis and biological activity of 2-(functionalised ethenyl, oxyiminomethyl and alpha by Clear, NJ, Davies, JS, Eglington, AJ, Fell, SC, Hinks, JD, Hird, NW, Hunt, E, Moss, SF, Pearson, MJ

    Published in Journal of antibiotics
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  2. 2
    Syntheses based on 1,2-secopenicillins; the synthesis of the 1-oxadethiapenem ring system

    Syntheses based on 1,2-secopenicillins; the synthesis of the 1-oxadethiapenem ring system by Eglington, A. John

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  3. 3
    β-Lactamase-stable penicillins. Synthesis and structure-activity relationships of (Z)-alkyloxyimino penicillins ; selection of BRL 44154

    β-Lactamase-stable penicillins. Synthesis and structure-activity relationships of (Z)-alkyloxyimino penicillins ; selection of BRL 44154 by BROWN, P, CALVERT, S. H, PEARSON, M. J, PONSFORD, R. J, SYMS, J. V, CHAPMAN, P. C. A, COSHAM, S. C, JOHN EGLINGTON, A, ELLIOT, R. L, HARRIS, M. A, HINKS, J. D, LOWTHER, J, MERRIKIN, D. J

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  4. 4
    Conversion of the olivanic acids into antibiotics of the PS-5 type: use of a new carboxy protecting group

    Conversion of the olivanic acids into antibiotics of the PS-5 type: use of a new carboxy protecting group by Corbett, David F., Eglington, A. John

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  5. 5
    Structure--activity relationships in cephalosporins prepared from penicillins. 2. Analogues of cephalexin substituted in the 3-methyl group

    Structure--activity relationships in cephalosporins prepared from penicillins. 2. Analogues of cephalexin substituted in the 3-methyl group by Brain, E G, Eglington, A J, James, B G, Nayler, J H, Osborne, N F, Pearson, M J, Smale, T C, Southgate, R, Tolliday, P, Basker, M J, Mizen, L W, Sutherland, R

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  6. 6
    Structure elucidation of MM 17880, a new fused β-lactam antibiotic isolated from Streptomyces olivaceus; a mild β-lactam degradation reaction

    Structure elucidation of MM 17880, a new fused β-lactam antibiotic isolated from Streptomyces olivaceus; a mild β-lactam degradation reaction by Corbett, David F., Eglington, A. John, Howarth, T. Trefor

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