1966
DOI: 10.1021/ja00956a051
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The Total Synthesis of Cephalosporin C1

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Cited by 373 publications
(116 citation statements)
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“…Alternatively, the ketone 8 was isolated, then converted into the en01 acetates by acetic anhydride in the presence of hydrogen bromide. Addition of bromine to the en01 acetates, followed by aqueous work-up gave the bromo ketone 11 I n contrast to the behavior of the etdo isomer, the action of lithium in ammonia on the exo isomer 6 only resulted in reduction of the carbonyl group.…”
mentioning
confidence: 97%
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“…Alternatively, the ketone 8 was isolated, then converted into the en01 acetates by acetic anhydride in the presence of hydrogen bromide. Addition of bromine to the en01 acetates, followed by aqueous work-up gave the bromo ketone 11 I n contrast to the behavior of the etdo isomer, the action of lithium in ammonia on the exo isomer 6 only resulted in reduction of the carbonyl group.…”
mentioning
confidence: 97%
“…De-N-methylation of N-methyl anatoxin using 2,2,2-trichloroethoxycarbonyl chloride ( 11) proved to be erratic, and the zinc deblocking of the nitrogen was not clean, so this method was not pursued further.…”
mentioning
confidence: 99%
“…[98,106,115,217,218] 63 Für die Synthese des Pyridylthiazols 160 wurde das aus L-Cystein abgeleitete Thioamid 47 [98] mit dem -Bromketon 161 [219] …”
Section: Untersuchungen Zur Hetero-diels-alder-reaktionunclassified
“…However, the latter method is not suitable for tertiary diols, due to the instability of the corresponding chloroformates [12]. But activation of tertiary and other diols is possible with carbonyldiimidazole [13] or with 4-nitrophenylchloroformate [14] and both methods have been applied [3,5] successfully to the synthesis of labile polycarbonates.…”
Section: Preparation Of Polycarbonute 3amentioning
confidence: 99%