The Enantiomeric Separation of Tetrahydrobenzimidazoles Cyclodextrins‐ and Cyclofructans. Issue 2 (13th December 2012)
- Record Type:
- Journal Article
- Title:
- The Enantiomeric Separation of Tetrahydrobenzimidazoles Cyclodextrins‐ and Cyclofructans. Issue 2 (13th December 2012)
- Main Title:
- The Enantiomeric Separation of Tetrahydrobenzimidazoles Cyclodextrins‐ and Cyclofructans
- Authors:
- Perera, Sirantha
Na, Yun‐Cheol
Doundoulakis, Thomas
Ngo, Victor J.
Feng, Qing
Breitbach, Zachary S.
Lovely, Carl J.
Armstrong, Daniel W. - Abstract:
- <abstract abstract-type="main"> <title>ABSTRACT</title> <p>High performance liquid chromatography (HPLC) and capillary electrophoresis (CE) were used to examine the enantiomeric separation of a series of 17 racemic tetrahydrobenzimidazole analytes. These compounds were prepared as part of a synthetic program directed towards a select group of pyrrole‐imidazole alkaloids. This group of natural products has a unique framework of pyrrole‐ and guanidine‐containing fused rings which can be constructed through the intermediacy of a tetrahydrobenzimidazole scaffold. Several bonded cyclodextrin‐ (both native and derivatized) and derivatized cyclofructan‐based chiral stationary phases were evaluated for their ability to separate these racemates via HPLC. Similarly, several cyclodextrin derivatives and derivatized cyclofructan were evaluated for their ability to separate this set of chiral compounds via CE. Enantiomeric selectivity was observed for the entire set of racemic compounds using HPLC with resolution values up to 3.0. Among the 12 different CSPs, enantiomeric recognition was most frequently observed with the Cyclobond RN and LARIHC CF6‐P, while the Cyclobond DMP yielded the greatest number of baseline separations. Fifteen of the analytes showed enantiomeric recognition in CE with resolution values as high as 5.0 and hydroxypropyl‐γ‐cyclodextrin was the most effective chiral additive. <italic>Chirality 25:133–140</italic>, 2013. © 2012 Wiley Periodicals, Inc.</p> </abstract>
- Is Part Of:
- Chirality. Volume 25:Issue 2(2013:Feb.)
- Journal:
- Chirality
- Issue:
- Volume 25:Issue 2(2013:Feb.)
- Issue Display:
- Volume 25, Issue 2 (2013)
- Year:
- 2013
- Volume:
- 25
- Issue:
- 2
- Issue Sort Value:
- 2013-0025-0002-0000
- Page Start:
- 133
- Page End:
- 140
- Publication Date:
- 2012-12-13
- Subjects:
- Chirality -- Periodicals
Pharmaceutical chemistry -- Periodicals
541.22 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1520-636X ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chir.22127 ↗
- Languages:
- English
- ISSNs:
- 0899-0042
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3181.124450
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4104.xml