Neue β‐Lactam‐Antibiotika. Über Derivate der 3‐Hydroxy‐7‐amino‐ceph‐3‐em‐4‐carbonsäure. Modifikationen von Antibiotika, 10. Mitteilung [1]
- 6 November 1974
- journal article
- abstracts
- Published by Wiley in Helvetica Chimica Acta
- Vol. 57 (7), 1919-1934
- https://doi.org/10.1002/hlca.19740570705
Abstract
3‐Hydroxy‐ceph‐3‐em‐esters 5 a–c, versatile intermediates for the preparation of new β‐lactam antibiotics, were obtained by ozonolysis of the corresponding 3‐methylidene‐esters 3 a–c. Reduction and elimination gave the 3‐unsubstituted ester 13; derivatives 16 a–c and 20–22 resulted from O‐alkylation. The 3‐methoxy‐esters 16 a–c were converted into the corresponding acids 23 a–d. Several other transformations of the β‐ketoester system are described.This publication has 11 references indexed in Scilit:
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