Journal of the Chemical Society. Chemical communications p. 374 - 375 (1987)
Update date:2022-07-29
Topics:
Baldwin, Jack E.
Adlington, Robert M.
Coates, Janice B.
Crabbe, M. James C.
Keeping, John W.
et al.
Structural variants on the acylamino-side chains of penicillins as substrates for the ring expansion enzyme from Cephalosporium acremonium CO728 show that a six carbon chain terminating in a carboxy group permits efficient conversion into cephems with the expection of δ-(L-aminoadipoyl) <5-(5S)-amino-5-carboxypentanoyl>.
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