Endre søk
RefereraExporteraLink to record
Permanent link

Direct link
Referera
Referensformat
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Annet format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annet språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf
Herstellung von 6,14‐Ethenomorphinan‐Derivaten
Alkaloida Chemische Werke AG, Tiszavasvári, H-4440, Hungary.ORCID-id: 0000-0002-7552-1076
1993 (engelsk)Inngår i: Liebigs Annalen der Chemie, ISSN 0170-2041, Vol. 1993, nr 8, s. 915-919Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Preparation of 6,14‐Ethenomorphinane Derivatives Buprenorphine (5j) and diprenorphine (5k) were synthesized from N‐formyl‐northebaine (1c) and N‐benzyl‐northebaine (1d) via new intermediates. N‐cyclopropylmethyl‐dihydronorthevinone 3d is a suitable compound for the synthesis of both 5j and 5k. We carried out detailed 1H‐ and 13C‐NMR analysis of the new compounds. 

sted, utgiver, år, opplag, sider
Wiley , 1993. Vol. 1993, nr 8, s. 915-919
HSV kategori
Identifikatorer
URN: urn:nbn:se:kth:diva-317768DOI: 10.1002/jlac.1993199301144Scopus ID: 2-s2.0-84988122333OAI: oai:DiVA.org:kth-317768DiVA, id: diva2:1695791
Merknad

QC 20220915

Tilgjengelig fra: 2022-09-14 Laget: 2022-09-14 Sist oppdatert: 2022-09-15bibliografisk kontrollert

Open Access i DiVA

Fulltekst mangler i DiVA

Andre lenker

Forlagets fulltekstScopus

Person

Szabó, Zoltan

Søk i DiVA

Av forfatter/redaktør
Szabó, Zoltan

Søk utenfor DiVA

GoogleGoogle Scholar

doi
urn-nbn

Altmetric

doi
urn-nbn
Totalt: 80 treff
RefereraExporteraLink to record
Permanent link

Direct link
Referera
Referensformat
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Annet format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annet språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf