Synthesis of nortropane alkaloid calystegine B


Journal

Carbohydrate research
ISSN: 1873-426X
Titre abrégé: Carbohydr Res
Pays: Netherlands
ID NLM: 0043535

Informations de publication

Date de publication:
15 Jan 2019
Historique:
received: 13 11 2018
revised: 04 12 2018
accepted: 04 12 2018
pubmed: 24 12 2018
medline: 5 6 2019
entrez: 23 12 2018
Statut: ppublish

Résumé

A new synthetic route for formation of a central cycloheptanone intermediate leading to the nortropane alkaloid calystegine B

Identifiants

pubmed: 30579118
pii: S0008-6215(18)30662-1
doi: 10.1016/j.carres.2018.12.002
pii:
doi:

Substances chimiques

Cycloheptanes 0
Methylglycosides 0
Nortropanes 0
Solanaceous Alkaloids 0
xylopyranose 0
calystegine B(2) 127414-85-1
Xylose A1TA934AKO
cycloheptanone QH80295937

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

122-126

Informations de copyright

Copyright © 2018 Elsevier Ltd. All rights reserved.

Auteurs

Emilie N Underlin (EN)

Department of Chemistry, Aarhus University, Langelandsgade 140, 8000, Aarhus C, Denmark.

Henrik H Jensen (HH)

Department of Chemistry, Aarhus University, Langelandsgade 140, 8000, Aarhus C, Denmark. Electronic address: hhj@chem.au.dk.

Articles similaires

Risk Assessment Plant Leaves Isomerism Humans Stereoisomerism
Corynebacterium glutamicum Tyramine Metabolic Engineering Phylogeny Fermentation

Expanding the antiprotozoal activity and the mechanism of action of n-butyl and iso-butyl ester of quinoxaline-1,4-di-

Alonzo González-González, Oscar Sánchez-Sánchez, Lilián Yépez-Mulia et al.
1.00
Giardia lamblia Trichomonas vaginalis Entamoeba histolytica Antiprotozoal Agents Quinoxalines
Xylitol Zea mays Polysaccharides Xylose Candida tropicalis

Classifications MeSH