Reaktionsgleichung
[NH2:1][C@@H:2]([C:5]([OH:7])=[O:6])[CH2:3]O.N[C@@H]([C:17]([OH:19])=O)CCCNC(=N)N.[NH2:20][C@@H](C(O)=O)CCSC.N[C@@H](C(O)=O)CCCCN.N[C@@H](C(O)=O)CC1C=CC=CC=1.N[C@@H](C(O)=O)CC(C)C.N[C@@H](C(O)=O)[C@@H](CC)C.N[C@@H](C(O)=O)CC1C2C(=CC=CC=2)NC=1.C(SSC[C@@H](N)C(O)=O)[C@@H](N)C(O)=O>>[NH2:1][C@H:2]([C:5]([OH:7])=[O:6])[CH2:3][C:17](=[O:19])[NH2:20]Komponenten
10
Versuchsvorschrift
According to a particularly advantageous further development of the invention the D-serine represented by X is replaced by D-arginine, D-methionine, D-lysine or D-phenylalanine, D-leucine, D-isoleucine, D-tryptophane or D-cystine.
Quellen und Nachweise
- ORD-Eintrag
- ord-a960b21c34a044a98fe5d817e6cb1437
- Quelldatensatz
- uspto-grants-1985_11
- Patentnummer
- US04555403
Verknüpfte Notizen
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