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- W2335726489 abstract "Die Umsetzung der Anile (I) mit den α-Bromestern (II) und Zn nach Reformatsky verlauft stereospezifisch zu den erythro-β-Aminosaureestern (III), die sich mit Athyl-MgBr zu den jeweiligen cis-β-Lactamen cyclisieren lassen." @default.
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- W2335726489 date "1973-11-06" @default.
- W2335726489 modified "2023-09-26" @default.
- W2335726489 title "ChemInform Abstract: REFORMATSKY-RK. VON SCHIFFSCHEN BASEN 2. MITT. SYNTHESE VON ERYTHRO-BETA-AMINOESTERN UND VON CIS-BETA-LACTAMEN" @default.
- W2335726489 doi "https://doi.org/10.1002/chin.197345307" @default.
- W2335726489 hasPublicationYear "1973" @default.
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