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- W2336366990 abstract "Veresterung der geschützten Aminosäuren (I) mit dem Indandion (II) in Gegenwart von DCC (Molverhältnis der Reaktionspartner 1:1 : l) liefert die aktivierten Ester (III), deren Aminolyse mit den Aminosäureestern (IV) unter Essigsäure-Katalyse zu den blockierten Dipeptidestern (V) führt." @default.
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- W2336366990 date "1980-11-18" @default.
- W2336366990 modified "2023-09-27" @default.
- W2336366990 title "ChemInform Abstract: 3-O-(N-ACYLAMINOACYL)HYDROXY-2-PHENYLINDENONES, PREPARATION AND USE IN THE SYNTHESIS OF PEPTIDES" @default.
- W2336366990 doi "https://doi.org/10.1002/chin.198046328" @default.
- W2336366990 hasPublicationYear "1980" @default.
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