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...
Main Authors: | Baldwin, J, Adlington, R, Aplin, R, Crouch, N, Schofield, C, Ting, H |
---|---|
פורמט: | Journal article |
שפה: | English |
יצא לאור: |
1987
|
פריטים דומים
-
The mechanism of the enzymatic ring expansion of penicillin N to deacetoxycephalosporin C
מאת: Crouch, N, et al.
יצא לאור: (1988) -
THE ENZYMATIC RING EXPANSION OF PENICILLINS TO CEPHALOSPORINS - SIDE-CHAIN SPECIFICITY
מאת: Baldwin, J, et al.
יצא לאור: (1987) -
ENZYMATIC RING EXPANSION OF PENICILLINS TO CEPHALOSPORINS - SIDE-CHAIN SPECIFICITY
מאת: Baldwin, J, et al.
יצא לאור: (1987) -
Probing the penicillin sidechain selectivity of recombinant deacetoxycephalosporin C synthase.
מאת: Dubus, A, et al.
יצא לאור: (2001) -
Substrate specificity of cloned deacetoxycephalosporin C/deacetylcephalosporin C synthetase.
מאת: Baldwin, J, et al.
יצא לאור: (1988)