STEPWISE HYDROGEN REMOVAL IN THE ENZYMATIC RING EXPANSION OF PENICILLIN-N TO DEACETOXYCEPHALOSPORIN-C
Reaction of a 1:1 mixture of penicillin N and 2,2-bis(trideuteriomethyl) penicillin N with partially purified deacetoxy-cephalosporin C/deacetylcephalosporin C synthetase from Cephalosporium acremonium CO 728 resulted in preferential conversion of the protiated substrate, whereas in similar experime...
المؤلفون الرئيسيون: | Baldwin, J, Adlington, R, Aplin, R, Crouch, N, Schofield, C, Ting, H |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
1987
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مواد مشابهة
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The mechanism of the enzymatic ring expansion of penicillin N to deacetoxycephalosporin C
حسب: Crouch, N, وآخرون
منشور في: (1988) -
THE ENZYMATIC RING EXPANSION OF PENICILLINS TO CEPHALOSPORINS - SIDE-CHAIN SPECIFICITY
حسب: Baldwin, J, وآخرون
منشور في: (1987) -
ENZYMATIC RING EXPANSION OF PENICILLINS TO CEPHALOSPORINS - SIDE-CHAIN SPECIFICITY
حسب: Baldwin, J, وآخرون
منشور في: (1987) -
Probing the penicillin sidechain selectivity of recombinant deacetoxycephalosporin C synthase.
حسب: Dubus, A, وآخرون
منشور في: (2001) -
Substrate specificity of cloned deacetoxycephalosporin C/deacetylcephalosporin C synthetase.
حسب: Baldwin, J, وآخرون
منشور في: (1988)