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February 1, 1963Biochemical JournalOpen Access

Biosynthesis of cephalosporin C from amino acids

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Abstract

Schmidt reaction to ornithine. The results showed that almost all the 14C in the c-aminoadipic acid was localized in C-6.

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Cite This Study

TROWN et al. (1963) studied this question.

synapsesocial.com/papers/6a8ce676233da3a613eaa0b1 https://doi.org/10.1042/bj0860284

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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1α-Oxoglutarate as a precursor of the d -α-aminoadipic acid residue in cephalosporin CReview · 1963 · 28 citations
2Further degradation products of cephalosporin C. Isolation and synthesis of 2-(4-amino-4-carboxybutyl)thiazole-4-carboxylic acidReview · 1960 · 30 citations
3The structure of cephalosporin CReview · 1961 · 297 citations
4Isotopic Carbon: Techniques in Its Measurement and Chemical ManipulationOriginal Research · 1949 · 38 citations
5Synthesis of d -δ-amino-δ-carboxyvalerylglycine (a degradation product of cephalosporin N) and of dl -δ-amino-δ-carboxyvaleramideReview · 1954 · 35 citations