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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1086978Erstellt: 26. Oktober 2026

Aspidospermidine-3-carboxylic acid, 4-(acetyloxy)-6,7-didehydro-3-hydroxy-16-methoxy-1-methyl-, methyl ester, (2beta,3beta,4beta,5alpha,12beta,19alpha)- → 3',4'-Anhydrovinblastine

https://huagongshe.com/reaction/1086978

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAspidospermidine-3-carboxylic acid, 4-(acetyloxy)-6,7-didehydro-3-hydroxy-16-methoxy-1-methyl-, methyl ester, (2beta,3beta,4beta,5alpha,12beta,19alpha)-HCID 16596—
Edukt(+)-CatharanthineHCID 5458190—
Produkt3',4'-AnhydrovinblastineHCID 443324—

Reaktionsschritte

In J. Am. Chem. Soc./98:22/Oct. 27, 1976, Langlois et al describe a process in which the monomers catharanthine and vindoline are coupled to form AVLB. The coupling is performed using a peracid to generate first the N-oxide of catharanthine, followed by Polonovski-type fragmentation of the N-oxide initiated with addition of trifluoroacetic anhydride to form a dimer. A reducing agent such as sodium borohydride is then added to generate AVLB which can be isolated e.g. chromatographically.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05034320
Quelldatensatzuspto-grants-1991_07
ORD IDord-e7abaf1b05c040e8a2584989826f2ee9
Quellennotizuspto-grants-1991_07