100Å -
Analytical Columns
The chiral phases, DNB-LEU or DNB-PHGLY,
are prepared from N-3,5-dinitrobenzoyl protected derivatives of leucine
or phenylgylcine. These phases are available in both the D- or the L-
enantiomers of the amino acids.
The unique feature of amino-acid-derived
chiral phases is that the elution order of enantiomers in the sample is
dependent on the D- or L- chirality of the bonded amino acid. Therefore,
the order of elution can be controlled by appropriate selection of
stationary phase. This can be of tremendous advantage for those samples
which contain a large excess of one enantiomer, in which case it is
desirable to have the minor component elute first.
Many racemic acids and amines which
cannot be resolved in their native form can be easily converted to
amides or anilides which can be resolved by an amino-acid-derived chiral
phase. The following compounds are candidates for amino-acid-derived
chiral phases:
Aromatic alcohols |
Aryl substituted phthalides |
Aromatic amino acids |
Aryl substituted lactams |
Aromatic amino alcohols |
Aryl substituted succinamides |
Aromatic thiols |
Aryl substituted hydantoins |
Aromatic arnines |
Aryl acetamides |
Aromatic sulfoxides |
Hydroxy-aryl phosphonates |
Mandelic acid analogs |
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