Asymmetric solution-phase mixture aldol reaction using oligomeric ethylene glycol tagged chiral oxazolidinones

Article abstract of DOI:10.1016/j.tetlet.2017.04.026

Sorting tags are oligomeric structures that can be used as protecting groups or chiral auxiliaries enabling solution-phase mixture syntheses of multiple tagged compounds in one pot and allowing for facile and predictable chromatographic separation of products at the end of synthetic sequences. Perfluorinated hydrocarbon and oligomeric ethylene glycol (OEG) derivatives are known classes of sorting tags. Herein we describe the preparation of OEGylated chiral oxazolidinones and their use in asymmetric solution-phase mixture aldol reactions. Through the use of such oxazolidinones based on tyrosine four different individually tagged aldol adducts were obtained as a mixture, chromatographically demixed, detagged, and it was shown that these processes gave the desired aldol products in good yield and enantioselectivity.

Full text of DOI:10.1016/j.tetlet.2017.04.026

Accepted Manuscript
Asymmetric solution-phase mixture aldol reaction using oligomeric ethylene
glycol tagged chiral oxazolidinones
Serhan Turkyilmaz, Craig S. Wilcox
PII:
S0040-4039(17)30456-2
DOI:
http://dx.doi.org/10.1016/j.tetlet.2017.04.026
TETL 48818
Reference:
Tetrahedron Letters
To appear in:
Received Date:
Revised Date:
Accepted Date:
2 March 2017
3 April 2017
5 April 2017
Please cite this article as: Turkyilmaz, S., Wilcox, C.S., Asymmetric solution-phase mixture aldol reaction using
oligomeric ethylene glycol tagged chiral oxazolidinones, Tetrahedron Letters (2017), doi: http://dx.doi.org/10.1016/
j.tetlet.2017.04.026
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Asymmetric solution-phase mixture aldol reaction using oligomeric ethylene glycol tagged
chiral oxazolidinones
Serhan Turkyilmaza,b and Craig S. Wilcoxa,*
aDepartment of Chemistry, University of Pittsburgh, Pittsburgh, PA 15260, USA
bDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Istanbul University, 34116 Beyazit, Istanbul, Turkey
* Corresponding author. Tel.: +1 4126248269; fax: +1 4126248611; e-mail: daylite@pitt.edu
Abstract
Sorting tags are oligomeric structures that can be used as protecting groups or chiral auxiliaries enabling solution-
phase mixture syntheses of multiple tagged compounds in one pot and allowing for facile and predictable
chromatographic separation of products at the end of synthetic sequences. Perfluorinated hydrocarbon and
oligomeric ethylene glycol (OEG) derivatives are known classes of sorting tags. Herein we describe the preparation
of OEGylated chiral oxazolidinones and their use in asymmetric solution-phase mixture aldol reactions. Through the
use of such oxazolidinones based on tyrosine four different individually tagged aldol adducts were obtained as a
mixture, chromatographically demixed, detagged, and it was shown that these processes gave the desired aldol
products in good yield and enantioselectivity.
Keywords
Solution-Phase Mixture Synthesis
Oligomeric Ethylene Glycol
Evans Aldol Reaction
Oxazolidinone
Sorting Tag
Page 1 of 9

Introduction
Drawbacks associated with solid-phase organic synthesis have prompted a search for alternative methods for the
generation of libraries of structurally diverse compounds. Such methods include liquid phase organic synthesis1a,b
along with solution-phase strategies such as the generation of indexed combinatorial libraries2a-c and approaches
involving the use of phase tags such as precipitons,3a-c boronic acid derivatives,4 and fluorous synthesis.5a-g Among
these alternative methods fluorous synthesis is particularly important as it provides for a reliable strategy, termed
Fluorous Mixture Synthesis (FMS),6a-i allowing for the mixture synthesis of target structures and their separation
into individual products at the end of the synthetic sequence. This is accomplished through labelling of each
substrate with a fluorocarbon sorting tag of unique chain length, taking mixtures of these tagged substrates through a
number of synthetic steps, and separation (i.e. demixing) of these tagged substrates by chromatography with a
fluorous stationary phase where substrate elution order is dictated by the chain length of the sorting tag.
We have discovered that oligomeric ethylene glycol (OEG) derivatives can also be used as sorting tags.7a,b OEG
tags allow for the orderly and predictable demixing of a mixture of tagged substrates through chromatography on
regular silica gel where elution times are directly proportional to OEG chain length (Figure 1).7a Demixing
efficiency can be further enhanced by addition of lithium salts to silica gel (i.e. complexation chromatography).7a
OEG tags are particularly noteworthy because they are separable under orthogonal chromatographic conditions with
respect to fluorous tags. This chromatographic orthogonality allows for double tagging of substrates through which a
larger number of parallel solution-phase reactions can be carried out in the same reaction vessel compared to the use
of a single class of sorting tag.7c-d
Figure 1. Principle of solution-phase mixture synthesis using OEG-based sorting tags.
The aldol reaction is a very important method for C-C bond formation. Use of chiral oxazolidinones (i.e. Evans
auxiliaries) as chiral auxiliaries for asymmetric aldol reactions has been a seminal contribution to this area.8a-c The
high synthetic value of Evans auxiliaries made the preparation and application of OEG tagged chiral oxazolidinones
an attractive target for us. Chiral oxazolidinones derived from tyrosine were of particular interest as they allow for
straightforward derivatization with OEGs through etherification. In this communication we would like to report on
the preparation and application of OEG tagged chiral oxazolidinones derived from tyrosine.
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The objectives of this study were: i. The preparation of acylated-OEGylated chiral oxazolidinones 2a-d starting
from 1a-b; ii. Execution of mixture solution-phase aldol reactions of 2a-d with benzaldehyde; iii. Demonstration of
demixing of the products using chromatography on normal phase silica; iv. Stereochemical analysis of the aldol
products thus formed (3a-d) to establish the efficacy and suitability of these OEGylated chiral oxazolidinones for
asymmetric mixture aldol reactions. Structures 2a-d were targeted because they would maximize the
chromatographic resolution of products 3a-d. Aldol reactions with benzaldehyde were selected since the resulting
aldol adducts are known and thus would allow for facile assessment of the utility of OEGylated chiral
oxazolidinones (Scheme 1).
Scheme 1. Objectives of this study.
Results and Discussion
While a number of routes could be considered for the preparation of tyrosine based chiral oxazolidinones, we
found the method developed by Green et al. to be particularly convenient and high yielding.9 Boc protection of R-
and S-tyrosine (1a-b) followed by benzylation afforded the globally protected amino acids (4a-b) in good yields.
LiAlH4 reduction of 4a-b, NaH mediated oxazolidinone formation, and removal of the benzyl protecting group
through hydrogenation afforded chiral oxazolidinones 5a-b in good yields as well (Scheme 1). The optical rotation
of 5b (-11.2°) matched the values reported in the literature. The optical rotation of 5a (+11.2°) was, as expected, the
opposite of 5b (Scheme 2).
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O
O
O
HN
O
H2N
BocHN
OH
OBn
i, ii
iii, iv, v
OH
OBn
OH
5a
, R-, 83% (3 steps)
5b, S-, 77% (3 steps)
1a
, R-
1b, S-
4a
, R-, 90% (2 steps)
4b, S-, 77% (2 steps)
Scheme 2. i. Boc2O, dioxane:H2O (1:1), TEA, 20 °C, 20 h; ii. BnBr, K2CO3, Bu4NI, DMF, rt, 2 d; iii. LiAlH4, THF, 0 °C to rt, 2
h; iv. NaH, THF, rt, 24 h; v. Pd/C, H2, rt, 24 h.
OEGylation of oxazolidinones 5a-b was accomplished with acceptable yields through Cs2CO3/KI mediated
etherification with OEG-chlorides of varying chain lengths. Thus the R- isomers were tagged with OEG-1 and OEG-
3 (6a, 6c) and the S- isomers were tagged wth OEG-2 and OEG-4 (6b, 6d). 6a-b and 6c-d were acylated in good
yields with, respectively, butyryl and propionyl chloride using n-BuLi to give 2a-d (Scheme 3).8
O
O
O
R
N
O
HN
O
ii, iii
i
5a-b
OEGnMe
OEGnMe
6a, R-, n=1, 74%
6b, S-, n=2, 65%
6c, R-, n=3, 60%
6d, S-, n=4, 66%
2a, R-, n=1, R=Me, 89%
2b, S-, n=2, R=Me, 91%
2c, R-, n=3, R=H, 90%
2d, S-, n=4, R=H, 90%
Scheme 3. i. Cs2CO3, KI, Cl-OEGnMe, DMF, 60 °C, 24 h; ii. n-BuLi, THF, -78 °C, 20 min.; iii. RCH2CH2COCl, THF, -78 °C,
30 min.
With 2a-d in hand, mixture aldol reactions of these OEG-tagged substrates with benzaldehyde were carried out.
Enolization of a mixture of 2a-d using Bu2BOTf (1.8 eq.) and NEt3 (1.9 eq.), and subsequent addition of
benzaldehyde afforded a mixture of OEG-tagged aldol products 3a-d. This mixture was demixed using silica gel
flash column chromatography (Scheme 4). It is remarkable that it was possible to separate 9 compounds (4 products,
4 starting materials, and excess benzaldehyde) with good purity in a single run. Demixing was also demonstrated
using normal phase HPLC and a chromatogram for this separation is provided in Figure 2 (for chromatographic
parameters see Table SI-1, Supporting Information). Product elution times in either case were-as expected-directly
proportional to bound OEG chain length.
Page 4 of 9

Scheme 4. i. 1.8 eq. Bu2BOTf, 1.9 eq. NEt3, CH2Cl2, 0 °C, 10 min; ii. PhCHO, CH2Cl2, -78 °C to 0 °C, 2 h; iii. Demixing using
flash column chromatography on silica.
Figure 2. Panel A shows a normal phase HPLC chromatogram for a mixture of aldol adducts 3a-d (Conditions: 250 x 4.6 mm
Supelco Supelcosil silica column, gradient elution (1:1 EtOAc:hexanes for 5 min., then EtOAc to 5% IPA in EtOAc in 3 min.), 1
mL/min flow rate, UV-Vis detection). Panel B shows 2D-UV/Vis spectra demonstrating identical absorption profiles for the
chromatographic peaks corresponding to 3a-d (right to left).
Aldol products 7a-d were liberated from the OEG-tagged chiral auxiliaries using LiOOH (LiOH mixed with
H2O2).10 To facilitate the stereochemical analysis of these products they were converted to the corresponding methyl
esters 7a-d through reaction with freshly prepared diazomethane (CH2N2). Both steps proceeded with good to
excellent yields (Scheme 5).
OH
O
OH
O
ii
O
OH
i
3a-d
R
R
7a, 2,3-R-, R=Me, 83%
7b, 2,3-S-, R=Me, 87%
7c, 2,3-R-, R=H, 93%
7d, 2,3-S-, R=H, 91%
8a, 2,3-R-, R=Me, 99%
8b, 2,3-S-, R=Me, 99%
8c, 2,3-R-, R=H, 98%
8d, 2,3-S-, R=H, 99%
Scheme 5. i. LiOH, H2O2, THF:H2O (3:1), 0 °C, 2 h; ii. CH2N2, Et2O, 0 °C, 1 h.
Relative and absolute stereochemical configurations, and enantiomeric purities of 7a-d and 8a-d were
determined, respectively, using 1H-NMR, optical rotation measurements, and chiral HPLC. α-β hydrogen spin-spin
1
coupling constants (i.e. JAB) as determined through H-NMR indicated gauche conformations in all cases (i.e. JAB
<
6 Hz), thus it was inferred that syn-aldol products were obtained (Table SI-2, Supporting Information).11 Optical
rotation (i.e. [α]D) values for 7c-d and 8a-d matched those previously reported (Table SI-2, Supporting
Page 5 of 9

Information),12a-e and it was concluded that products with the expected absolute configuration were obtained. Chiral
HPLC analysis of 8a-d revealed enantiomeric excess (i.e. % ee) values of 99% for 8a, 98% for 8b, 94% for 8c, and
93% for 8d (Table SI-4, Supporting Information).
In this study we have demonstrated the preparation of OEG-tagged chiral oxazolidinones and have used them in
solution-phase mixture aldol reactions. The products obtained were easily demixed using silica gel flash column
chromatography. As the chromatogram in Figure 2 shows, even using an extremely steep gradient excellent baseline
resolution was observed between 3a-d. Thus it is conceivable that it would be possible to demix more than 4
products using just 4 OEG tags. We have observed that OEG tags were compatible with all reaction conditions
required in this work. Furthermore, aldol products were obtained in good yields and their stereochemical
configurations were identical to what would be expected of the corresponding products of single component
reactions. We believe that OEG-tagged protecting groups and chiral auxiliaries like 6a-d will be important tools in
the arsenal of chemists seeking to generate libraries of compounds through solution-phase mixture synthesis.
Acknowledgments: This work was supported by the National Institutes of Health (5R01GM068005).
Supplementary Information: Supplementary data (synthetic procedures, NMR data, and HPLC data) associated
with this article can be found, in the online version, at …
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Asymmetric solution-phase mixture aldol reaction using oligomeric ethylene glycol tagged
chiral oxazolidinones
Serhan Turkyilmaza,b and Craig S. Wilcoxa,*
aDepartment of Chemistry, University of Pittsburgh, Pittsburgh, PA 15260, USA
bDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Istanbul University, 34116 Beyazit, Istanbul, Turkey
* Corresponding author. Tel.: +1 4126248269; fax: +1 4126248611; e-mail: daylite@pitt.edu
Highlights
•
•
•
•
•
Oligomeric ethylene glycol (OEG) derivatives act as chromatographic sorting tags.
Chiral oxazolidinones tagged with OEGs of varying length were synthesized.
4 aldol products were synthesized in one pot using tagged chiral oxazolidinones.
Products were easily separated using silica gel flash column chromatography.
Aldol products were obtained with good yield and enantioselectivity.
Page 8 of 9

Asymmetric solution-phase mixture aldol reaction using oligomeric ethylene glycol tagged
chiral oxazolidinones
Serhan Turkyilmaza,b and Craig S. Wilcoxa,*
aDepartment of Chemistry, University of Pittsburgh, Pittsburgh, PA 15260, USA
bDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Istanbul University, 34116 Beyazit, Istanbul, Turkey
* Corresponding author. Tel.: +1 4126248269; fax: +1 4126248611; e-mail: daylite@pitt.edu
Graphical Abstract
Page 9 of 9