CA2571034A1 - New chiral columns with broad chiral selectivity - Google Patents

Abstract

A general chiral column with a multiple proline-based chiral stationary phase.

Description

NEW CHIRAL COLUMNS WITH BROAD CHIRAL SELECTIVITY
Government Support This invention was made in connection witll Grant Numbers NIH 1 RO 1 GM63 812-01 and NIH 1 R01 GM60637-01A1, from the National Institutes of Health. The United States Government has rights to this invention.

Field of the Invention The present invention relates to the field of chiral chemistry. More particularly, the present invention relates to the separation of enantiomers, i.e., those isomers in which the arrangement of atoms or groups is such that the two molecules are not superimposable.
The present inventor has developed a new class of chiral columns that can resolve a large number of racemic compounds. These columns are stable and can be used with a number of mobile phase solvents.
Background of the Invention Stereoisomers are those molecules which differ from each other only in the way their atoms are oriented in space. Stereoisomers are generally classified as diastereomers or enantiomers; the latter embracing those which are mirror-iinages of each other, the former being those which are not. The particular arrangement of atoms that characterize a particular stereoisomer is known as its optical configuration, specified by known sequencing rules as, for example, either + or - (also D or L) and/or R or S.
Though differing only in orientation, the practical effects of stereoisomerism are important. For example, the biological and pharmaceutical activities of many compounds are strongly influenced by the particular configuration involved. Indeed, many compounds are only of widespread utility when employed in a given stereoisomeric form.
Living organisms usually produce only one enantiomer of a pair. Thus only (-)-2-methyl-1-butanol is forined in yeast ferinentation of starches; only (+)-lactic acid is formed in the contraction of muscle; fruit juices contain only (-)-malic acid, and only (-)-quinine is obtained from the cinchona tree. In biological systems, stereochemical specificity is the rule rather than the exception, since the catalytic enzymes, which are so important in such systems, are optically active. For example, the sugar (+)-glucose plays an important role in animal metabolism and is the basic raw material in the fermentation industry; however, its optical counterpart, or antipode, (-)-glucose, is neither metabolized by animals nor fermented by yeasts. Other examples in this regard include the mold Penicillium glaucum, which will only consume the (+)-enantiomer of the enantiomeric mixture of tartaric acid, leaving the (-)-enantiomer intact.
Also, only one stereoisomer of chloromycetin is an antibiotic; and (+)-ephedrine not only does not have any drug activity, but it interferes with the drug activity of its antipode. Finally, in the world of essences, the enantiomer (-)-carvone provides oil of spearmint with its distinctive odor, while its optical counterpart (+)-carvone provides the essence of caraway.
Thus, as enzymes and other biological receptor molecules possess chiral structures, enantioiners of a racemic compound may be absorbed, activated, and degraded by them in different manners. This phenomenon causes that in many instances, two enantiomers of a racemic drug may have different or even opposite pharmacological activities. In order to aclcnowledge these differing effects, the biological activity of each enantiomer often needs to be studied separately. This and other factors within the pharmaceutical industry have contributed significantly to the need for enantiomerically pure compounds and thus the need for chiral chromatography.
Accordingly, it is desirable and oftentimes essential to separate stereoisomers in order to obtain the useful version of a coinpound that is optically active.
Separation in this regard is generally not a problem when diastereomers are involved:
diastereomers have different physical properties, such as melting points, boiling points, solubilities in a given solvent, densities, refractive indices etc. Hence, diastereomers are normally separated from one another by conventional metliods, such as fractional distillation, fractional crystallization or chromatography.
Enantiomers, on the other hand, present a special problem because their physical properties are identical. Thus they cannot as a rule--and especially so when in the form of a racemic mixture--be separated by ordinary methods: not by fractional distillation, because their boiling points are identical; not by conventional crystallization because (unless the solvent is optically active) their solubilities are identical; not by conventional chromatography because (unless the adsorbent is optically active) they are held equally onto the adsorbent. The problem of separating enantiomers is further exacerbated by the fact that conventional synthetic techniques almost always produce a mixture of enantiomers. When a mixture comprises equal amounts of enantiomers having opposite optical configurations, it is called a racemate;
separation of a racemate into its respective enantiomers is generally known as a resolution, and is a process of considerable importance.
Chiral columns that can resolve a large number of racemic compounds (general chiral columns) are in high demand. They are needed routinely in many laboratories, especially in pharmaceutical industry. Prior to the present invention, Daicel columns, macrocyclic antibiotic columns, and the Whelk-O coluinns were probably known as the industrial leaders in this type of general chiral columns. The present inventor has developed a new class of general chiral columns based on the use of proline and its analogues.
Furthermore; and importantly, the columns of the present invention have the capability of resolving at least a similar or higher percentage of the compounds tested.
Furthermore, the columns of the present invention provide better separation on some of the compounds tested and can resolve certain compounds that cannot be resolved with the commonly used commercial columns listed above.
The columns of the present inventions are stable and can be used with a large number of mobile phase solvents. Therefore, the columns of the present invention should find important applications as general chiral columns.
A large number of chiral columns have been prepared in the past; however, only a few demonstrated broad chiral selectivity. As stated above, the successful examples include the popular Daicel coluinns, the Chirobiotic columns, and the Whelk-O1/2 columns.
The Daicel colunms are prepared by coating sugar derivatives onto silica gel. Chirobiotic columns are prepared by immobilizing macrocyclic glycopeptides onto silica gel. Whelk-O
1/2 columns contain both electron rich and electron deficient aromatics. These columns have broad chiral selectivity and have been applied successfully to resolve a fair number of racemic compounds.
They have different selectivity and stability profiles. Their selectivities complement each other in some cases, while they duplicate each other in other cases. Some of the columns are more suited for reversed phase conditions and others for normal phase conditions. Each column has its own strengtlis and weaknesses. Despite these progresses, there are still many compounds that cannot be resolved or resolved well using these commercial available columns.
Therefore, there is still a significant need to develop new columns that have relatively broad chiral selectivity.
Summary of the Invention The present invention is directed to a chiral selector that represents an improvement in the art of enantiomeric separation. Tlius, one embodiment of the present invention is a general chiral column with a multiple proline-based chiral selector.
Another embodiment of the present invention is a chiral stationary phase made of peptides with 2 or more prolines, including chiral selectors with 2, 3, 4, 5, 6, or 10 prolines. Also included within the scope of the present invention are analogs and isomers of prolines, and analogs and isomers of the chiral selector compounds of the present invention.
Another embodiment of the present invention is a chiral stationary phase (or column) of the following formula:

end-capping Pro group linker Support n wherein n is any integer of 2 or greater, and analogs and isomers thereof.
Another embodiment of the present invention is where n is any integer from 2-10.

The separations achieved for analytes are comparable or superior to those achieved on Daicel AD, Daicel OD, and Whelk 02 columns. The multiple proline-based chiral columns of the present invention show promise as a superior general chiral column.

Brief Description of the Drawings Figure 1 shows the structure for amino acid L-Proline and its associated stationary phases Fmoc-Pro-(Me)Ahx-APS (CSP1), Fmoc-Pro2-(Me)Ahx-APS (CSP2), Fmoc-Pro4-(Me)Ahx-APS
(CSP3); and Fmoc-Pro6-(Me)Ahx-APS (CSP4). CSP2-4 are embodiments of compounds of the present invention.
Figure 2 shows the synthesis of one embodiment of the present invention, Fmoc-Pro4-(Me)Ahx-APS chiral stationary phase (CSP3): Synthesis of Fmoc-Pro4-(Me)Ahx-APS
chiral stationary phase (CSP3): (a) Fmoc-(Me)Ahx-OH, DIC; (b) (1) Piperidine; (2) Fmoc-Pro-OH, HATU; (c) AcOH; (d) aminopropyl-silica gel, HATU.

Description of the Invention The present inventor has developed a new chiral column that has relatively broad chiral selectivity, when compared witli Daicel columns and Whelk 02 column, as industry standards or industry models. Additionally, the chiral columns of the present invention are stable in a number of mobile phase conditions.
The success rate of the chiral column of the present invention compares well with the best commercially available general chiral columns developed over the last few decades. For 22 racemic compounds chosen based on their availability (see example 4), our Pro4 column (CSP 3) resolved 17 compounds; our Pro2 column (CSP2) resolved 16 compounds; our Pro6 column (CSP4) resolved 15 compounds. In comparison, Daicel OD column resolved 18, Daicel AD
resolved 16, and Whelk-02 resolved 15 compounds. The monoproline column (CSP1) is much less effective, as it can resolve only 6 out of the 22 compounds tested. The achieved resolutions with the monoproline column are also very modest.
Proline is a unique amino acid in many ways (Figure 1). Instead of having a primary amino group as in other a-amino acids, it contains a secondary amine. Because of the cyclic structure, rotation around the nitrogen-a-carbon bond is restricted. Also because of the cyclic structure, proline is not ideally suited for a-helix or P-sheet conformation;
instead, polyproline forms its own unique helical conformation (Polyproline I and polyproline II).
The ainide bond in polyproline is sterically hindered compared with other oligopeptides. The distinctly different conformational and structural features of polyprolines suggest that they may behave quite differently from other short oligopeptides that have been studied in chiral chromatography.
The present inventors discovered that proline based chiral selectors, including the embodiment tetraproline based chiral stationary phase 3 (Figure 1) , diproline based chiral stationary phase 2, hexaproline based chiral stationary phase 4 have relatively broad chiral selectivity, while mono-proline stationary phase 1 is largely ineffective.
Immobilization of the chiral selectors'of the present invention to silica gel is accomplished through a linker group. One example of a linker group of the present invention is a N-alkylamino group. A second example is a N-methylamino group. Another example is 6-N-methylaminohexanoic acid. The amide bond between these linlcers and proline residue is more sterically hindered due to the N-methyl or N-alkyl group. The particular linker group can be selected by one of ordinary skill in the art depending on the analyte to be tested. For example, when the selector Fmoc-Pro-Pro is immobilized using 6-N-methylaminohexanoic acid, it may resolve about 16 out of about 22 analytes tested. For the same chiral selector, when immobilized using 6-aminohexanoic acid, it resolved only 4 out of the same group of analytes.

Additionally, the stationary phase compounds of the present invention may comprise various end-capping groups as known in the art.
By use of the term proline with respect to the present invention, it is understood that analogs and isomers of proline are included. For example all stereoisomers are included.
Additionally, analogs are included. Examples of the analogs that are included herein are those with the following skeleton structure feature such as in D-proline, hydroxyproline, and pipecolinic acid:
X
n H Chiral Center wherein n is an integer (such as 1, 2, 3, 4, 5, etc.) and X is a heteroatom such as O,S,N; and other unspecified atoms can be carbon or heteroatoms.
These covalently bound columns of the present invention are stable in common organic solvents, including CH2C12 and CHC13. Therefore, a wide selection of mobile phase conditions could be applied in method development. For several analytes, the present inventor attempted resolution with CHzCl2/hexane as the mobile phase and effective separation was also achieved (example 6). Wider solvent choices have advantages in that some racemic analytes are soluble in only certain solvents and some compounds can be resolved better in certain solvents In terms of potential interaction modes with the analytes, examples of the chiral selectors of the present invention are forming attractive hydrogen bonds with the analyte and they may also have attractive polar interactions witli the analyte. In addition, steric interaction between analyte and chiral selector could also be important.

The following examples and experimental section are designed to be purely exemplary in nature. Thus, this section should not be viewed as being limiting of the present invention.

Examples Throughout this section, various abbreviations are used, including the following: DIC, diisopropylcarbodiimide; HATU, O-(7-Azabenzotriazol-1-yl)N,N,N',N'-tetramethyluronium hexafluorophosphate; DIPEA, N,N-Diisopropylethylamine; DMF, N,N-Dimethylformamide;
DCM, Dichloromethane; DMAP, 4-(dimethylaminopyridine); NMM: N-methylmorpholine;
Fmoc, 9-Fluorenylmethoxycarbonyl; (Me)Ahx: 6-methylaminohexanoic acid; Fmoc-(Me)Ahx-OH, 6-[(9H-fluoren-9-ylmethoxy)carbonyl]methylamino hexanoic Acid; Fmoc-Ahx-OH, 6-[(9H-fluoren-9-ylmethoxy)carbonyl]aminohexanoic acid; Fmoc-Pro-OH, N-a-Fmoc-L-proline..
General Supplies and Equipment:

Amino acid derivatives were purchased from NovaBiochem (San Diego, CA). All other chemicals and solvents were purchased from Aldrich (Milwaukee, WI), Fluka (Ronkonkoma, NY), or Fisher Scientific (Pittsburgh, PA). HPLC grade Kromasil silica gel (particle size 5 m, pore size 100 A, and surface area 298 m2/g) was purchased from Akzo Nobel (EKA
Chemicals, Bohus, Sweden). Selecto silica gel (32-63 gm) from Fisher Scientific was used for flash column chromatographic purification of target compounds. Thin-layer chromatography was completed using EM silica ge160 F-254 TLC plates (0.25 mm; E.Merck, Merck KGaA, 64271 Darmstadt, Germany). Elemental analyses were conducted by Atlantic Microlab, Inc.
(Norcross, GA).
HPLC analyses were completed with a Beckman analytical gradient system (System Gold). UV
spectra were obtained with a Shimadzu UV 201 spectrometer (cell volume 3 mL;
cell pass length 10 mm).

Exatnple 1: PrepaNation of chiral stationary phase Fmoc-PNo-(Me)Ahx-APS (CSP1) To 0.80 g of (Me)Ahx-APS silica (the surface (Me)Ahx concentration is 0.64 mmol/g) are added mixtures of Fmoc-Pro-OH (3 equiv., 0.52 g), HATU (3 equiv., 0.58 g), and DIPEA (3 equiv., 0.20 g) in 8 mL of DMF. After agitating for 6 h, the resulting silica is filtered and washed with DMF, Methanol, and DCM to yield the desired chiral stationary phase. The surface Pro concentration is determined to be 0.57 mmol/g based on the Fmoc cleavage method. The resulting chiral stationary phase is packed into a 50 x 4.6 mm HPLC column using a standard slurry packing method.

Example 2: Preparation of chiral stationary phase Fmoc-Pro2-(Me)Ahx APS (CSP2) To 0.80 g of (Me)Ahx-APS silica (the surface (Me)Ahx concentration was 0.64 mmol/g) were added mixtures of Fmoc-Pro-OH (3 equiv., 0.52 g), HATU (3 equiv., 0.58 g), and DIPEA (3 equiv., 0.20 g) in 8 mL of DMF. After agitating for 6 h, the resulting silica was filtered and washed with DMF, Methanol, and DCM. The surface Pro concentration was determined to be 0.55 mmol/g based on the Fmoc cleavage method. The Fmoc protecting group was then removed by treatment of the silica with 10 mL of 20% (V/V) piperidine in DMF for 1 h.
The deprotected silica, Pro-(Me)Ahx-APS, was collected by filtration and washed with DMF, Methanol, and DCM. Then another module, Fmoc-Pro-OH, was coupled to the resulting silica following an identical reaction sequence and yielded the desired chiral selector on the silica gel. The surface Fmoc concentration was determined to be 0.52 mmol/g based on the Finoc cleavage method. The resulting chiral stationary phase was packed into a 50 x 4.6 mm HPLC column using the standard slurry packing method.

Example 3: Preparation of chiral stationary phase Fmoc-PN04-(Me)Ahx-APS (CSP3) To Rink acid resin (100-200 mesh, 3.0 g, 0.43 mmol/g) preswelled with DCM (20 mL, 30 min) was added the mixture of Fmoc-(Me)Ahx-OH (1.42 g, 3.87 mmol), DMAP (0.16 g,1.29 mmol), NMM (0.39 g, 3.87 mmol), and DIC (0.49 g, 3.87 mmol) in DCM-DMF(1:1 V/V, 10 mL). After agitating for 6 h, the resin was collected by filtration and washed with DMF, DCM, and Methanol (20 mL x 3). The Fmoc group was then removed by treatment with 20 mL of 20%
(V/V) piperidine in DMF for 30 min. The deprotected (Me)Ahx-O-Rink resin was collected and washed with DMF, DCM, and Methanol (20 mL x 3).

To (Me)Ahx-O-Rink resin was added the mixture of Fmoc-Pro-OH (1.31 g, 3.87 mmol), HATU (1.47 g, 3.87 mmol), and DIPEA (0.50 g, 3.87 mmol) in 20 mL of anhydrous DMF. After agitating for 3 h, the resin was filtered and washed with DMF, DCM, and Methanol (20 mL x 3).
The Fmoc group was then removed and the second, third and fourth modules, Fmoc-Pro-OH, were coupled by following exactly the same procedures as described above to yield the desired Fmoc-(Pro)4-(Me)Ahx-O-Rink resin.

The resin was then treated with 1% TFA in DCM (20 mL, 10 min) to release Finoc-(Pro)4-(Me)Ahx-OH from the resin. This cleavage reaction was repeated one more time to ensure complete reaction. The crude product obtained was purified by flash column chromatography on silica gel (mobile phase: 5% Methanol in DCM) to yield the desired Fmoc-(Pro)4-(Me)Ahx-OH as a white solid (0.90 g, 92%). 'H NMR (CD2C12): 8 1.2-1.7 (m, 6H), 1.9-2.4 (m, 18H), 2.80 (s, 3H), 3.2-3.6 (m, 1011), 4.2-4.7 (m, 7H), 7.1-7.6 (m, 8H), 9.6 (br, 1H). ESI-MS: m/z 756.0 (M+H").

A mixture of Fmoc-(Pro)4-(Me)Ahx-OH (0.90 g, 1.19 mmol), HATU (0.45 g, 1.19 mmol), and DIPEA (0.15 g, 1.19 mmol) in 8 mL of anhydrous DMF was added to 0.7 g of 3-aininopropyl silica gel (APS). APS was prepared from Kromasil silica gel (5 m spherical silica, 100 A, 298 m2/g) and 3-aminopropyltriethoxysilane. The surface amino concentration is 0.66 mmol/g, based on elemental analysis data of nitrogen (C, 3.11; H, 0.83; N, 0.93). After agitating the mixture for 4 h, the stationary phase was collected by filtration and washed with DMF, DCM, and Methanol (10 mL x 3). The surface Fmoc concentration was determined to be 0.27 mmol/g based on Fmoc cleavage method. The resulting chiral stationary phase was packed into a 50 x 4.6 mm HPLC
column using the standard slurry packing method.

The following examples set forth various chromatographic measurements.
Therein, retention factor (k) equals to (tr-t0)/t0 in which tr is the retention time and t0 is the dead time.
The separation factor (a) equals k2/kl, ratio of the retention factors of the two enantiomers.
Separation factor of 1 indicates no separation. The larger the separation factor, the better the separation is. Dead time t0 was measured with 1,3,5-tri-t-butylbenzene as the void volume marker. Flow rate at 1 inL/min., UV detection at 254 nin.
Example 4 This example compares chromatographic resolution of racemic compounds with chiral columns, including embodiments of the present invention (Pro2 (CSP2), Pro4 CSP3), Pro6(CSP4)).
In the following table, kl is the retention factor of the least retained enantiomer and the separation factor (a) is defined earlier This example also shows that a mono-proline chiral column does not perform sufficiently.
Furthermore, this example shows embodiments of the present invention in comparison with known commercial columns.

Table 1. Chromatographic resolution of racemic compounds with chiral columns.
kl is the retention factor of the least retained enantiomer. Mobile phases are solutions of specified percentage of IPA and acetic acid in hexanes.

Analyte name Analyte Structure Prol Pro2 Pro4 Pro6 Daicel Daicel Whelk-Benzoin oH a:l a: 1.07 a: 1.09 a:1.12 a: 1.61 a:1.32 a: 2.12 k1:5.78 k1:8.22 k1:6.35 k1:16.0 k1:4.68 k1:3.46 k1:1.83 I\ \ 3%IPA 3%IPA 3%IPA 5%IPA 3%IPA 15%IPA 5%IPA
O
Hydrobenzoin OH / a:l a: 1.12 a: 1.13 a:1.15 a:l a: 1.08 a: 1.33 \ k1:17.7 k1:21.15 kl:17.9 k1:25.79 k1:7.35 k1:5.15 k1:4.18 I\ 1 4%IPA 8 8%IPA 4%IPA 8%IPA 4%IPA
OH 4%IPA 4%IPA
Benzoin oxime OH / a: 1 a: 1.09 a: 1.13 a: 1.20 a: 1.13 a: 1.24 a: 1.31 k1:12.2 ki:16.08 kl:15.3 k1:41.45 k1:2.82 k1:4.55 11:1.40 8 20%IPA 6 30%IPA 10%IPA 15%IPA 10%IPA
N 20%IP 20%IP
oH A A
2,2,2-Trifluoro-l- a:l a:1.28 a: 1.56 a: 1.78 a:1.13 a: 1.47 a: 1.13 (9-anthryl) I k1:16.4 k1:23.44 kl:18.4 k1:22.58 k1:1.26 k1:1.99 k1:0.62 ethanol \ \ / 0 l0%IPA 8 25%IPA 15%IPA 10%IPA 10%IPA

10%IP 10%IP

a- \ a:1 a:1.06 a:1.10 a:1.10 a:1.16 a:1.11 a:1 (pentafluoroethyl} I k1:19.3 k1:16.08 k1:8.91 k1:8.62 k1:0.90 k1:0.79 k1:0.70 a-(trifluoromethyl)- ~ 1 3%IPA 3%IPA 5%IPA 1%IPA 3%IPA 3%IPA
Benzenemethanol 3%IPA

Warfarin \ a:l a:1.11 a:1.08 a:1.18 a:2.49 a:3.94 a:1.97 I k1:13.9 k1:10.57 k1:11.1 k1:17.50 k1:6.40 k1:5.02 k1:10.06 1 10%IPA 9 10%IPA 15%IPA 20%IPA 20%IPA
OH O 10%IP & 10%IP &
A& 1% A& 1%
1% AcOH 1% AcOH
AcOH AcOH
Sec-Phenethyl a: l a: 1.02 a: 1.02 a: 1.04 a: 1.37 a: I a: 1.03 alcohol k1:6.67 k1:11.3 k1:8.07 k1:19.42 k1:8.30 k1:4.12 k1:3.64 OH 1%IPA 1%IPA 1%IPA 1%IPA 1%IPA 2%IPA 2%IPA
in in hexane in in hexane in hexane in hexane in hexane hexane hexane a-Methyl-2- a: 1 a: 1 a:1.04, a: 1 a:1 a: 1.05 a: 1.02 Naphthalene k1:13.3 k1:22.36 kl:17.6 kl:18.81 k1:6.25 k1:1.98 k1:4.39 methanol / I \ OH 6 1%IPA 2 3%IPA 3%IPA 10%IPA 3%IPA
1%IPA 1%IPA

1-Acenaphthenol OH a: a:1 a: 1 a:1 a:1.16 a: 1.08 a: 1.28 k1:7.83 k1:13.36 kt:10.2 k1:28.06 k1:5.46 k1:6.58 k1:4.96 3%IPA 3%IPA 8 3%IPA 3%IPA 3%IPA 3%IPA
3%IPA

3-Phenyl-Glycidol a: 1 a:1 a: 1 a:1 a: 1.15 a: 1 a: 1.37 o k1:5.23 k1:5.64 k1:6.77 k1:10.38 k1:16.87 k1:8.01 k1:8.74 3%IPA 3%IPA 3%IPA 5%IPA 10%IPA 8%IPA 10%IPA

1,1'-si-2-naphthol a: 1.04 a: 1.16 a: 1.29 a: 1.42 a: 1.16 a: 1.13 a: 1 kt:11.4 k1:32.80 k1:23.8 k1:9.94 k1:4.49 k1:3.58 k1:1.26 OH 8 75%IPA 3 90%IPA 8%IPA 25%IPA 5%IPA
75%IP 75%IP
/ I \ OH A A

2,2'-Diol- a:1.14 a:1.17 a:1.32 a:1.67 a:1.32 a:1 a:1 5,5',6,6',7,7',8,8'- kt:12.5 k1:1 1.10 k1:10.9 kt:19.75 k1:3.98 k1:8.53 k1:4.47 octahydro-1,1'-binaphthalene / OH 8 10%IPA 5 25%IPA 5%IPA 10%IPA 5%IPA
OH 10%IP 10%IP
A A

1,2,3,4-Tetrahydro- oMe a: 1.05 a: 1.18 a: 1.24 a: 1.20 a:1.15 a:1.40 a: 1.16 4- k 14.8 k 18.68 k 12.6 k 23.53 k 2.13 Ic 3.44 k1:2.27 4 methox~hen 1 ~ 1 ~ ~ t i (" y)-6-methyl-2-thioxo- I 15%IPA 0 15%IPA 15%IPA 15%IPA 15%IPA
5-pyrimidine 0 15%IP 15%IP
carboxylic acid NH A A
ethyl ester EtO
N~S
1,2,3,4-Tetrahydro- a: 1.12 a: 1.20 a: 1.41 a: 1.32 a: 1.30 a:1.36 a: 1 4- kt:44.6 k1:27.80 k1:25.0 k1:30.13 k1:2.87 k1:4.62 k1:2.23 (4-hydroxyphenyl)- I
6 50%IPA 7 70%IPA 15%IPA 15%IPA 15%IPA
6-methyl-2-thioxo-5-Pyrimidine 30%IP 30%IP
carboxylic acid ~ A A
ethyl ester NH
Et0 N ~S
1-[1,2,3,4- OMe a:1 a: 1.20 a: 1.21 a: 1.34 a: 1.18 a:1.70 a: 1 Tetrahydro-4- k1:27.0 k1:40.60 k1:25.7 k1:33.90 k1:2.62 k1:3.62 k1:1.83 (4-methoxyphenyl)- 3 15%IPA 2 25%IPA 15%IPA 15%IPA 15%IPA
6-methyl-2-thioxo-5-pyrimidinyl] 15%IP 15%IP
ethanone A A
Ac NH

I N~S
Hexobarbital M. a: 1 a:1 a:1 a: 1 a:1.12 a:1.46 a: 1 ~ k1:28.8 k1:22.28 kt:16.9 kt:11.26 k1:6.26 lc1:2.42 k1:1.95 e~N e 6 1%IPA 8 3%IPA 5%IPA 8%IPA 5%IPA
HN 1 %IPA 1 %IPA

M.
O

Temazepam Ph Ci a: 1.09 a:1 a:1 a:1 a:l a:1 a:1.19 N/ I\ k1:22.0 k1:25.54 k1:20.2 k1:25.52 k1:3.39 k1:4.12 k1:3.40 3 2%IPA 4 5%IPA 25%IPA 25%IPA 25%IPA
H ~ 2%IPA 2%IPA
~_N
5-Methyl- a:1 a: 1.16 a: 1.17 a: 1.34 a: 1.08 a:1 a: 1.11 5-(2,5-dichloro ~NH k1:11.2 k1:14.6 k1:8.55 k1:11.64 k,:4.29 k1:4.80 k1:1.96 phenyl) HN 1 15%IPA 15%IP 25%IPA 8%IPA 8%IPA 10%IPA
15%IP A
hydantoin A
CI
CI
5-Methyl-5-phenyl a: 1 a: 1.10 a: 1.15 a: 1.32 a: 1.09 a:l a: 1.46 hydantoin ~NH kl:16.2 k1:25.00 k1:15.6 k1:10.7 k1:4.06 k1:3.24 k1:1.67 HN 4 8%IPA 8%IPA 20%IPA 8%IPA 8%IPA 10%IPA
O 8%IPA

Mephenytoin ~_N a:1 a:1.14 a:1.14 a:1.27 a:1.10 a:1.37 a:1 k1:5.86 k1:7.86 k1:6.93 k1:9.85 k1:5.20 k1:3.56 k1:3.35 HN 2%IPA 2%IPA 2%IPA 3%IPA 4%IPA 4%IPA 4%IPA
O
Et sec-Butyl O i a: 1 a:1 a: 1 a: a:1 a:1.04 a: 1.05 carbanilate ~N ~ I k1:3.62 k1:7.30 k1:7.64 k1:15.34 k1:6.18 k1:3.35 k1:3.36 H 1%IPA 1%IPA 1%IPA 3%IPA 2%IPA 2%IPA 1%IPA
Methyl Mandelate OH a: 1.02 a: 1.10 a: 1.17 a: 1 a: 1.25 a:1.08 a: 1.07 k1:7.97 k1:10.8 k1:8.31 k1:17.49 k1:2.82 k1:1.85 k1:1.12 COOMe 1%IPA 1%IPA 1%IPA 3%IPA 3%IPA 10%IPA 10%IPA
Example 5: Specific embodiments, for exemplary purposes, of the stationaNy phase compounds of the present invention and silica supports.
This example sets forth poly-proline compounds of the present invention, including embodiments with different end-capping groups. The end-capping groups are bonded to the nitrogen atom that is further away from the support. As is noted in the example, some end-capping groups such as pivaloyl (PIV) (CSP-6) are more effective for some analytes tlian others, such as TAPA. Overall, several different end-capping groups useable with the present invention such as Piv, Fmoc, Boc, Cbz, Aca, Dmb, Tpa all work well. CSP-5, which has no end-capping group, did not perform as well with respect to some analytes.

Pro-Pro-N(Me)-Ahx-APS: CSP-5 NH

\ H
'---$/O O
N N_"~Si ~ Si02 Et0 Piv-Pro-Pro-N(Me)-Ahx-APS: CSP-6 ~Iyo AO
C N

N Si02 EtO
Fmoc-Pro-Pro-N(Me)-Ahx-APS:CSP-2 O~O
N
\'' O O
H
N
~ Si02 N EtO
I

Boc-Pro-Pro-N(Me)-Ahx-APS: CSP-7 O

N
O

N~ Si02 N Et0 Cbz-Pro-Pro-N(Me)-Ahx-APS: CSP-8 p O~O
N

\ II H

i E10 O

Aca-Pro-Pro-N(Me)-Ahx-APS: CSP-9 N
O H

Si02 N EtO
z I
O
Tapa-Pro-Pro-N(Me)-Ahx-APS: CSP-10 o-N

--IYO NOZ
N
\ //O
/ O H
N N/\/Si~ SiOg I EtO
I
Dinb-Pro-Pro-N(Me)-Ahx-APS: CSP-11 / I
~ O
N
\'' O 0 H I
N~~ si ~ SiO2 EtO I
O
Tpa-Pro-Pro-N(Me)-Ahx-APS: CSP-12 Fl- 0 \\, ~! 0 H
N\~ N~/Si~ Si02 Et0 Table 2. Impact of end-capping groups.

Analyte name CSP-5 CSP-6 CSP-2 CSP-7 CSP-8 CSP-9 CSP-10 CSP-11 CSP-12 Benzoin a: 1 a: 1.12 a: 1.07 a: 1.07 a: 1.08 a: 1 a: 1 a: 1.10 a: 1.07 k1:5.84 k1:6.34 k1:8.22 k1:4.45 k1:4.63 k1:7.71 k1:19.0 k1:7.76 k1:6.00 3%IPA 3%IPA 3%IPA 3%IPA 3%IPA 3%IPA 2 3%IPA 3%IPA
3%IPA
Hydrobenzoin a: 1.07 a: 1.22 a: 1.12 a: 1.11 a: 1.11 a: 1.10 a:1.14 a:1.13 a:1.16 kl:16.7 k1:17.0 k1:21.15 k1:10.71 k1:13.33 k1:16.8 k1:26.4 kl:18.09 k1:15.17 1 0 4%IPA 4%IPA 4%IPA 1 1 4%IPA 4%IPA
4%IPA 4%IPA 4%IPA 4%IPA
Benzoin oxime a: 1 a: 1.12 a: 1.09 a: 1 a: 1 a: 1 a: 1 a: 1.10 a: 1.08 k1:11.4 k1:14.6 k1:16.08 k1:10.09 k1:12.23 kl:13.4 k1:16.0 1c1:15.00 k1:11.71 4 5 20%IPA 20%IPA 20%IPA 4 3 20%IPA 20%IPA
20%IP 20%IP 20%IP 20%IP
A A A A
2,2,2-Trifluoro-l- a: 1 a: 1.58 a: 1.28 a: 1.28 a: 1.33 a:1.16 a: 1.28 a: 1.30 a:1.40 (9-anthryl) k1:17.2 k1:22.4 k1:23.44 k1:15.08 kl:15.82 k1:20.0 k1:31.5 k1:20.47 k1:16.03 ethanol 3 10%IP 10%IPA 10%IPA 10%IPA 2 9 10%IPA 10%IPA
10%IP A 10%IP 40%IP
A A A
a- a: 1 a:1.14 a: 1.06 a: 1.11 a: 1.10 a: 1.06 a: 1.10 a: 1.09 a: 1.09 (pentafluoroethyl) k1:9.72 k1:8.89 k1:16.08 k1:7.55 k1:5.76 k1:6.18 k1:8.13 k1:13.80 k1:5.75 3%IPA 3%IPA 3%IPA 3%IPA 3%IPA 3%IPA 3%IPA 3%IPA 3%IPA
a-(trifluoromethyl)-Benzenemethanol Warfarin a: 1 a: 1.20 a: 1.11 a:1 a:1.16 a: 1.12 a:1 a: 1.16 a: 1.14 k1:41.1 k1:12.4 k1:10.57 k1:19.53 kl:11.55 k1:14.3 k1:28.6 kl:13.41 k1:12.68 0 1 10%IPA 25%IPA 10%IPA 4 1 25%IPA 10%IPA
90%IP 10%IP & & 10%IP 10%IP &
A A& 1% 1% A& A& 1%
1% AcOH AcOH 1% 1% AcOH
AcOH AcOH AcOH
Sec-Phenethyl a:1 a: 1.08 a:1.02 a: 1.03 a: 1 a: 1 a: 1 a: 1 a: 1 alcohol k1:6.47 k1:8.42 k1:11.3 k1:6.30 k1:6.02 k1:6.84 k1:9.37 k1:19.34 k1:1.90 1%IPA 1%IPA 1%IPA 1%IPA 1%IPA 1%IPA 1%IPA 1%IPA 1%IPA
a-Methyl-2- a:1 a:1 a:1 a:1 a:1.02 a:1.10 a:1 a:1.04 a:1 Naphthalene k1:15.3 k1:17.3 k1:22.36 k1:13.07 kl:12.96 k1:14.8 k1:17.1 k1:7.65 k1:1.19 methanol 0 1 1%IPA 1%IPA 1%IPA 9 5 1%IPA 1%IPA
1 %IPA 1 %IPA 1 %IPA 5%IPA
1-Acenaphthenol a: 1 a: 1 a: 1 a:1 a: 1 a: 1 a: 1 a:1 a:1 k1:8.12 k1:10.7 k1:13.36 k1:7.34 k1:8.45 kj:11.0 k1:21.4 k1:13.90 k1:8.95 3%IPA 8 3%IPA 3%IPA 3%IPA 4 1 3%IPA 3%IPA
3%IPA 3%IPA 7%IPA
3-Phenyl- a: 1 a:1 a: 1 a: 1 a: 1 a: 1 a: 1 a:1 a:1 Glycidol k1:9.54 k1:11.1 k1:5.64 k1:10.75 k1:9.12 k1:11.2 k1:20.8 k1:15.49 k1:9.78 3%IPA 3 3%IPA 3%IPA 3%IPA 9 5 3%IPA 3%IPA
3%IPA 3%IPA 3%IPA
1,1'-Bi-2- a: 1.05 a: 1.34 a: 1.16 a: 1.17 a: 1.17 a: 1.35 a: 1 a: 1.18 a:
1.30 naphthol k1:13.3 k1:20.9 k1:32.80 kl:13.21 k1:17.07 ki:15.7 k1:28.6 k1:21.89 k1:19.51 1 0 75%IPA 75%IPA 75%IPA 3 3 75%IPA 75%IPA
75%IP 75%IP 75%IP 75%IP
A A A A
2,2'-Dio1- a:1 a:1.08 a: 1.17 a: 1.06 a: 1.14 a: 1.33 a: 1.34 a: 1.24 a: 1 5,5',6,6',7,7',8,8'- k1:13.0 k,:17.9 k1:11.10 k1:8.80 k,:12.16 k,:12.3 k1:7.83 k,:13.54 k,:12.73 octahydro-1,1'- 3 2 10%IPA 10%IPA 10%IPA 3 10%IP 10%IPA 10%IPA
binaphthalene 10%IP 10%IP 10%IP A
A A A
1,2,3,4- a: 1 a: 1.30 a: 1.18 a:1.19 a:1.15 a: 1.22 a: 1.48 a: 1.21 a: 1.26 Tetrahydro-4- k1:11.5 k,:11.3 ki:18.68 k1:7.91 k1:12.93 k1:13.3 k1:23.0 k1:12.98 k1:9.61 (4 2 4 15%IPA 15%IPA 15%IPA 6 7 15%IPA 15%IPA
methoxyphenyl)-6-methyl-2- 10%IP 15%IP 15%IP 15%IP
thioxo- A A A A
5-pyrimidine carboxylic acid ethyl ester 1,2,3,4- a: 1.07 a: 1.49 a: 1.20 a: 1.40 a: 1.36 a: 1.37 a: 1.26 a: 1.40 a:
1.36 Tetrahydro-4- k1:36.7 k1:39.0 k1:27.80 k1:23.11 k1:31.14 k1:27.1 k1:28.5 k1:24.64 k1:16.80 (4 2 0 50%IPA 30%IPA 30%IPA 8 6 40%IPA 30%IPA
hydroxyphenyl)-6-methyl-2- 70%IP 30%IP 30%IP 40%IP
thioxo-5- A A A A
Pyrimidinecarbox ylic acid ethyl ester 1-[1,2,3,4- a: 1 a: 1.29 a: 1.20 a: 1.24 a: 1.11 a: 1.34 a:1 a: 1.34 a: 1.23 Tetrahydro-4- k1:26.5 k1:26.2 k1:40.60 k1:19.00 k1:32.93 k1:31.7 k1:50.8 k1:34.45 k1:17.30 (4 4 7 15%IPA 15%IPA 15%IPA 2 5 15%IPA 15%IPA
methoxyphenyl)-6-methyl-2- 10%IP 15%IP 15%IP 15%IP
thioxo- A A A A
5-pyrimidinyl]
etlianone Hexobarbital a:1 a:1 a:1 a:1.22 a:1.10 a:1 a:1 a:1 a:1 k1:29.9 kt:11.5 k1:22.28 k1:7.21 k1:13.11 k1:15.0 k1:9.74 k1:14.94 kl:15.27 2 1 1%IPA 1%IPA 1%IPA 2 2%IPA 1%IPA 1%IPA
1%IPA 1%IPA 1%IPA
Temazepam a: 1 a: 1 a: 1 a:1 a: 1 a: 1 a: 1 a: 1 a: 1 k1:20.7 kl:17.7 k1:25.54 kl:12.52 k1:17.34 k1:27.7 k1:25.4 k1:20.24 k1:27.30 7 3 2%IPA 2%IPA 2%IPA 5 4 2%IPA 2%IPA
2%IPA 2%IPA 2%IPA 10%IP
A
5-Methyl- a: 1 a: 1.30 a: 1.16 a:1 a:1 a:1 a: 1 a: 1.22 a: 1.16 5-(2,5-dichloro k1:9.35 k1:10.0 kl:14.6 k1:12.39 kl:15.78 k1:8.27 k1:7.52 kt:9.91 k1:7.30 phenyl)hydantoin 10%IP 0 15%IPA 15%IPA 15%IPA 15%IP 15%IP 15%IPA 15%IPA
A 15%IP A A
A
5-Methyl-5- a:1 a:1.18 a:1.10 a:1.08 a:1.16 a:1 a:1.16 a:1.10 a:1 phenyl k1:18.1 k1:17.9 k1:25.00 kl:12.93 kl:14.71 kt:13.5 k1:13.4 k1:19.00 kt:14.25 hydantoin 2 1 8%IPA 8%IPA 8%IPA 4 4 8%IPA 8%IPA
8%IPA 8%IPA 8%IPA 8%IPA
Mephenytoin a: 1 a: 1 a: 1.14 a:1 a:1 a:1 a: 1.10 a:1 a: 1.07 k1:7.42 k1:5.73 k1:7.86 k1:5.43 k1:5.43 k1:6.27 k1:9.74 k1:8.09 k1:9.00 2%IPA 2%IPA 2%IPA 2%IPA 2%IPA 2%IPA 2%IPA 2%IPA 2%IPA
sec-Butyl a:1.47 a:1 a:1 a:1.04 a:1 a:1 a:1 a:1 a:l carbanilate k1:4.09 k1:9.04 k1:7.30 k1:5.91 k1:5.91 k1:7.74 k1:11.8 k1:9.64 k1:9.61 1%IPA 1%IPA 1%IPA 1%IPA 1%IPA 1%IPA 9 1%IPA 1%IPA
1%IPA
Methyl a:1 a:1.23 a:1.10 a:1 a:1 a:1.10 a:1 a:1 a:1 Mandelate k1:9.24 k1:9.00 k1:10.8 k1:6.50 kt:8.46 k1:6.27 k1:19.3 k1:19.00 k1:17.64 1%IPA 1%IPA 1%IPA 1%IPA 1%IPA 1%IPA 7 1%IPA 1%IPA
1%IPA

Exanaple 6 This example compares chromatographic resolution of racemic compounds with Fmoc-Pro-Pro-Pro-Pro-N(Me)Ahx-APS (CSP-3) which is an embodiment of the present invention, in two mobile phase systems. Accordingly, this example helps demonstrate the flexibility of chiral stationary phases of the present invention in different mobile phase systems.
Table 3. Chromatographic resolution of racemic compounds with Fmoc-Pro-Pro-Pro-Pro-N(Me)Ahx-APS (CSP-3) in two mobile phase systems Analyte name IPA/Hex DCM/Hex/MeOH
Benzoin a: 1.09 a: 1.07 k1:6.35 k1:11.61 3%IPA 5%DCM
in Hexane Hydrobenzoin a:1.13 a:1.12 k1:17.98 k1:12.93 4%IPA 40%DCM
in Hexane Benzoin oxime a: 1.13 a: 1.08 k1:15.36 k1:15.85 20%IPA 100%DCM
2,2,2-Trifluoro-l- a: 1.56 a: 1.20 (9-anthryl) k1:18.48 k1:9.54 ethanol 10%IPA 100%DCM

a-(pentafluoroethyl)- a: 1.10 a: 1.06 a-(trifluoromethyl)- k1:8.91 k1:28.23 Benzenemethanol 3%IPA 30%DCM
in Hexane Warfarin a: 1.08 a:1 kt:11.19 k1:5.84 10%IPA & 30%DCM
1% in Hexane&
AcOH 1 %AcOH
Sec-Phenethyl a: 1.02 a: 1.02 alcohol k1:8.07 kl:13.08 1%IPA 10%DCM
in Hexane a-Methyl-2- a:1.04 a:1 Naphthalenemethanol kt:17.62 kt:23.66 1%IPA 10%DCM
in Hexane 1-Acenaphthenol a: 1 a: I
k1:10.28 kt:7.31 3%IPA 30%DCM
in Hexane 3-Phenyl-Glycidol a.:1 a: 1 k1:6.77 k1:7.39 3%IPA 30%DCM
in Hexane 1,1'-Bi-2-naphthol a: 1.29 a: 1.06 k1:23.83 kl:12.21 75%IPA 1 %MeOH
in Hexane 2,2'-Diol- a:1.32 a: 1 5,5',6,6',7,7',8,8'- k1:10.95 k1:12.08 octahydro-1,1'-binaphthalene 10%IPA 50%DCM
in Hexane 1,2,3,4-Tetrahydro4- a: 1.24 a:1.18 (4-methoxyphenyl)- kl:12.60 k1:6.26 6-methyl-2-thioxo- 15%IPA 60%DCM
5-pyrimidinecarboxylic acid ethyl ester in Hexane 1,2,3,4-Tetrahydro-4- a: 1.41 a:1.19 (4-hydroxyphenyl)- k1:25.07 kl:12.72 6-methyl-2-thioxo-5- 30%IPA 3%MeOH
Pyrimidinecarboxylic acid ethyl ester in Hexane 1-[1,2,3,4-Tetrahydro-4- a:1.21 a: 1.22 (4-methoxyphenyl)- kt:25.72 k1:12.20 6-methyl-2-thioxo- 15%IPA 60%DCM
5-pyrimidinyl]ethanone in Hexane Hexobarbital a:l a: 1 k1:16.98 k1:8.08 1 %IPA 30%DCM
in Hexane Temazepam a: 1 a: 1 k1:20.24 k1:4.62 2%IPA 10%DCM
in Hexane 5-Methyl- a:1.17 a:1.12 5-(2,5-dichloro k1:8.55 kl:13.56 phenyl)hydantoin 15%IPA 100%DCM
5-Methyl-5-phenyl a: 1.15 a:1.11 hydantoin kl:15.6 kl:18.51 8%IPA\ 100%DCM
Mephenytoin a:1.14 a:1.17 k1:6.93 k1:17.10 2%IPA 20%DCM in Hexane sec-Butyl carbanilate a: 1 a: 1.12 k1:7.64 k1:4.16 1%IPA 10%DCM in Hexane Methyl Mandelate a: 1.17 a: 1 k1:8.31 k1:8.18 1 %IPA 1 0%DCM in Hexane The invention being described, it will be apparent to those skilled in the art that various modifications and variations can be made in the present invention without departing from the scope or spirit of the invention. Other embodiments of the invention will be apparent to those skilled in the art from consideration of the specification and practice of the invention disclosed herein. It is intended that the Attachments be considered as exemplary only, and not intended to limit the scope and spirit of the invention.

Unless otherwise indicated, all numbers expressing quantities of ingredients, properties such as molecular weight, reaction conditions, experimental results, and so forth used in the Specification and Attachments are to be understood as being modified by the term "about."
Accordingly, unless specifically indicated to the contrary, are approxiinations that may vary depending upon the desired properties sought to be obtained by the present invention.
References The following references are incorporated by reference in their entirety.
(1) Stinson, S. C. Chemical & Engineering News 1995, 73, 44-74.
(2) Okamoto, Y.; Kawashima, M.; Hatada, K. Journal of the American Chemical Society 1984, 106, 5357-5359.
(3) Yashima, E.; Yamamoto, C.; Okamoto, Y. Journal of the Ainerican Chemical Society 1996, 118, 4036-4048.
(4) Berthod, A.; Chen, X.; Kullman, J. P.; Armstrong, D. W.; Gasparrini, F.;
D'Acquarica, I.;
Villani, C.; Carotti, A. Analytical Chemistry 2000, 72, 1767-1780.
(5) Ekborg-Ott, K. H.; Wang, X.; Armstrong, D. W. Microchetnical Journal 1999, 62, 26-49.
(6) Welch, C. J. Journal of Chromatography A 1994, 666, 3-26.
(7) Dobashi, A.; Dobashi, Y.; Kinoshita, K.; Hara, S. Analytical Chemistry 1988, 60, 1985-1987.
(8) Billiot, E.; Warner, I. M. Analytical Chemistry 2000, 72, 1740-1748.
(9) Wang, Y.; Li, T. Analytical Chemistry 1999, 71, 4178-4182.
(10) Poole, C. F.; Poole, S. K. Chromatography today; Elsevier: New York, 1991.
(11) Creighton, T. E. Proteins. Structures and Molecular Properties. 2nd ed;
W. H. Freeman and Company: New York, 1993.
(12) Carpino, L.; El-Faham, A.; Minor, C. A.; Albericio, F. Journal of the Chemical Society, Chemical Communications 1994, 201-203.

Claims (16)

1. A chiral stationary phase compound of the following formula:
wherein n is any integer of 2 or greater, and analogs and isomers thereof.

2. The chiral stationary phase compound of claim 1, wherein n is any integer from 2 to 10.

3. The chiral stationary phase compound of claim 1, wherein the support is a silica support.

4. The chiral stationary phase compound of claim 1, wherein the linker is an N-alkylamino group.

5. The chiral stationary phase compound of claim 4, wherein the linker is an N-methylamino group.

6. The chiral stationary phase compound of claim 4, wherein the linker is a 6-methylaminohexanoic acid group.

7. The chiral stationary phase of a compound of claim 1, wherein the end-capping group is a Piv, Fmoc, Boc, Cbz, Aca, Tapa, Dmb, or a Tpa group.

8. The chiral stationary phase of claim 1, wherein the linker is of the following formula:
wherein n is an integer, and R is an alkyl group including methyl group.

9. The chiral stationary phase compound of claim 1, wherein the linker is of the following formula:

10. The chiral stationary phase compound of claim 1, wherein the end-capping group is a Piv, Fmoc, Boc group.

11. The chiral stationary phase compound of claim 1, of the following formula:

and analogs and isomers thereof.

12. A chiral selector of the formula:
wherein n is any integer of 2 or greater, and analogs and isomers thereof.

13. A process for separating enantiomeric mixtures by liquid chromatography, comprising:
providing a racemic mixture;
providing a chiral column that comprises an optically active multi-proline compound or an analog or isomer thereof; and introducing the mixture to the chiral column.

14. The process of claim 13, wherein the optically active multi-proline compound is of the following formula:

wherein n is any integer of 2 or greater, and analogs and isomers thereof.

15. The process of claim 13, wherein the optically active multi-proline compound is of the following formula:

and analogs and isomers thereof.

16. A chiral stationary phase compound of claim 1, of the following formula.

Fmoc-Pro-Pro-(Me)N-(CH2)5CO-NH(CH2)3Silica (CSP2);
Fmoc-Pro-Pro-Pro-Pro-(Me)N-(CH2)5CO-NH(CH2)3Silica (CSP3);
Fmoc-Pro-Pro-Pro-Pro-Pro-Pro-(Me)N-(CH2)5CO-NH(CH2)3Silica (CSP4);
and analogs and isomers thereof.