Role of the weak interactions in enantiorecognition of racemic dihydropyrimidinones by novel brush-type chiral stationary phases.

Abstract:

:The chiral discrimination ability of two recently prepared chiral stationary phases (CSP 1 and CSP 2), based on a leucine derived chiral selector, was tested for the enantiomers of dihydropyrimidone (DHPM) derivatives and compared with the commercially available Hyun-leucine CSP 3 and classical Pirkle-leucine CSP 4. By combining all of these CSPs, the enantiomers of all DHPM derivatives used in this study can be properly resolved. Particularly good enantioresolutions were achieved for thioureide derivatives, such as Monastrol. The results presented show that sulfur-aromatic interactions are meritorious for these very good separations.

journal_name

Chirality

journal_title

Chirality

authors

Forjan DM,Gazić I,Vinković V

doi

10.1002/chir.20396

subject

Has Abstract

pub_date

2007-06-01 00:00:00

pages

446-52

issue

6

eissn

0899-0042

issn

1520-636X

journal_volume

19

pub_type

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