Published April 2018
| Version v1
Journal article
Synthesis and characterization of new conjugates of betulin diacetate and bis(triphenysilyl)betulin with substituted triazoles
- 1. Palacky University in Olomouc, Faculty of Medicine and Dentistry, Institute of Molecular and Translational Medicine (Czech Republic)
Description
A set of 12 new conjugates of betulin diacetate and bis(triphenysilyl)betulin with substituted triazoles was synthesized via bromination of the position 30 followed by the substitution of the bromoderivatives with sodium azide and reaction of the 30-azidobetulin derivatives with organic alkynes via Huisgen 1,3-cycloaddition. All 15 new compounds (3 intermediates and 12 triazoles) were fully characterized; however, attempts to evaluate their cytotoxicity were impossible due to limited solubility in testing media. Graphical abstract: .
Additional details
Identifiers
Publishing Information
- Journal Title
- Monatshefte fuer Chemie
- Journal Volume
- 149
- Journal Issue
- 4
- Journal Page Range
- p. 839-845
- ISSN
- 0026-9247
- CODEN
- MOCHAP
Conference
- Title
- 17. blue Danube symposium on heterocyclic chemistry
- Dates
- 30 Aug - 2 Sep 2017
- Place
- Linz (Austria)
INIS
- Country of Publication
- Austria
- Country of Input or Organization
- Austria
- INIS RN
- 50003502
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; S77: NANOSCIENCE AND NANOTECHNOLOGY;
- Resource subtype / Literary indicator
- Conference
- Descriptors DEI
- ALKYNES; AZIDES; BROMINATION; SODIUM; SOLUBILITY; SYNTHESIS; TOXICITY; TRIAZOLES
- Descriptors DEC
- ALKALI METALS; AZOLES; CHEMICAL REACTIONS; ELEMENTS; HALOGENATION; HETEROCYCLIC COMPOUNDS; HYDROCARBONS; METALS; NITROGEN COMPOUNDS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2018 Springer-Verlag GmbH Austria, part of Springer Nature