S Caccamese, G Principato
Index: J. Chromatogr. A. 893(1) , 47-54, (2000)
Full Text: HTML
The four enantiomeric pairs of vincamine group alkaloids were separated by HPLC using Chiralpak AD as chiral stationary phase (CSP) and various n-hexane-2-propanol and n-hexane-ethanol mobile phases. (+)-cis-Vincamine, which is used in pharmaceutical preparations, is eluted much faster than its optical isomer, with separation factors of 2.4 and 3.5, respectively in these mobile phases. Other CSPs gave negative results. A chiral recognition mechanism is proposed and circular dichroism spectra of the individual enantiomers are presented.
| Structure | Name/CAS No. | Molecular Formula | Articles |
|---|---|---|---|
![]() |
Vincamine
CAS:1617-90-9 |
C21H26N2O3 |
|
Mechanochemical activation of vincamine mediated by linear p...
2013-09-27 [Eur. J. Pharm. Sci. 50(1) , 56-68, (2013)] |
|
Determination of terpenoid indole alkaloids in hairy roots o...
2015-01-01 [Phytochem. Anal. 26 , 331-8, (2015)] |
|
Plasma Pharmacokinetics of Polyphenols in a Traditional Japa...
2015-01-01 [Molecules 20 , 18031-46, (2015)] |
|
Smart stability-indicating spectrophotometric methods for de...
2008-01-01 [J. AOAC Int. 91(2) , 299-310, (2008)] |
|
Alpneumines A-H, new anti-melanogenic indole alkaloids from ...
2010-06-15 [Bioorg. Med. Chem. 18(12) , 4415-21, (2010)] |
Home | MSDS/SDS Database Search | Journals | Product Classification | Biologically Active Compounds | Selling Leads | About Us | Disclaimer
Copyright © 2024 ChemSrc All Rights Reserved
