Abstract
An approach to the synthesis of epoxides based on 6-hydroxymethylpyridoxine acetals was developed. The epoxides obtained were involved in the ring opening reactions by nitrogen-, oxygen-, and sulfur-containing nucleophiles. Cytotoxicity and antiadrenergic properties of some synthesized compounds were studied on the models in situ and in vivo.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 519-531 |
| Number of pages | 13 |
| Journal | Russian Chemical Bulletin |
| Volume | 65 |
| Issue number | 2 |
| DOIs | |
| State | Published - Feb 1 2016 |
All Science Journal Classification (ASJC) codes
- General Chemistry
Fingerprint
Dive into the research topics of 'Synthesis and antiadrenergic properties of β-substituted alcohols based on 6-hydroxymethylpyridoxine'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver