Synthetic studies on α,α-disubstituted amino acids employing (2S,4R)-4-hydroxyproline as the chiral pool: Preparation of methyl o-benzyl-2-(α-cyanomethyl)-D-tyrosinate and dimethyl 2-(4-hydroxybenzyl)- L-aspartate

Article abstract of DOI:10.3987/COM-12-S(N)9

Methyl O-benzyl-2-(α-cyanomethyl)-D-tyrosinate and dimethyl 2-(4-hydroxybenzyl)-L-aspartate were synthesized starting from (2S,4R)-4-hydroxyproline Via Beckmann fragmentation of the corresponding oxime tosylate.

Full text of DOI:10.3987/COM-12-S(N)9

HETEROCYCLES, Vol. 86, No. 1, 2012, pp. -. © 2012 The Japan Institute of Heterocyclic Chemistry
Received, 9th April, 2012, Accepted, 30th May, 2012, Published online, 30th May, 2012
DOI: 10.3987/COM-12-S(N)9
SYNTHETIC STUDIES ON -DISUBSTITUTED AMINO ACIDS
EMPLOYING (2S,4R)-4-HYDROXYPROLINE AS THE CHIRAL POOL:
PREPARATION
(-CYANOMETHYL)-D-TYROSINATE
2-(4-HYDROXYBENZYL)-L-ASPARTATE
OF
METHYL
O-BENZYL-2-
AND
DIMETHYL
Ryohei Nagahara, Chihiro Hisa, Noriko Kojima, Naoshi Yamamoto, and
Toshio Honda*
Faculty of Pharmaceutical Sciences, Hoshi University, Ebara 2-4-41,
Shinagawa-ku, Tokyo 142-8501, Japan
Abstract – Methyl O-benzyl-2-(-cyanomethyl)-D-tyrosinate and dimethyl
2-(4-hydroxybenzyl)-L-aspartate
were
synthesized
starting
from
(2S,4R)-4-hydroxyproline via Beckmann fragmentation of the corresponding
oxime tosylate.
Recently we have developed a novel method for synthesis of a coccinellid alkaloid, (-)-adalinine,1 in
which (2S,4R)-4-hydroxyproline was recognized to be an important chiral template for constructing the
quaternary carbon center having an amino group at its -position, stereoselectively.
These results prompted us to utilize (2S,4R)-4-hydroxyproline as the chiral pool for preparation of
disubstituted amino acids, where a newly developed regioselective bond cleavage reaction between
the 4 and 5 positions of a proline ring was involved as a key step.
Thus, we decided to prepare 2-(-cyanomethyl)-D-tyrosine and 2-(4-hydroxybenzyl)-L-aspartic acid as
valuable chiral building blocks in the synthesis of biologically active compounds including natural
products.
We envisioned that an -substituted aspartic acid derivative could be obtained by hydrolysis of the
corresponding nitrile, O-benzyl-2-(-cyanomethyl)-D-tyrosine derivative. The desired nitrile would be
derived from the oxime tosylate of the 2,2-disubstituted 4-ketoproline derivative by application of
Beckmann fragmentation,2,3 in which a regioselective bond cleavage between the 4 and 5 positions would
be involved as depicted in Scheme 1. The desired 2,2-disubstituted 4-ketoproline might be prepared from
the 4-hydroxyproline derivative by a stereoselective alkylation.4,5

Scheme 1. Retrosynthetic analysis of 2-(4-hydroxybenzy)-L-aspartic acid and
2-(-cyanomethyl)-D-tyrosine
Thus, (2S,4R)-4-hydroxyproline (1) was converted to methyl (2S,4S)-4-{[tert-butyl(dimethyl)silyl]oxy}-
pyrrolidine-2-carboxylate (2) according to the literature procedures.6
HO
TBDMSO
TBDMSO
ref. 5
TBAF
THF
LiN(TMS)2
OBn
N
H
N
N
CO2H
CO2Me
CO2Me
Boc
Boc
OBn
Cl
(2S,4R)-4-hydroxy-
proline (1)
2
3
THF
1) aq. NaOH
2) DCC, DMAP
CHCl3
O
O
HO
HO
NaOMe
MeOH
OBn
OBn
N
N
N
CO2Me
OBn
CO2Me
Boc
Boc
Boc
4
5
6
OTs
(COCl)2
DMSO
Et3N
OH
N
N
O
OBn
OBn
OBn
NH2OH/HCl
TsCl
CH2Cl2
N
N
N
CO2Me
CO2Me
CO2Me
DIPEA
DMAP
CHCl3
Boc
Boc
pyridine
EtOH
Boc
9
7
8
Scheme 2. Synthesis of oxime tosylates (9)
A stereoselective alkylation of 2 with 4-benzyloxybenzyl chloride7 was carried out by adopting Nagumo’s
protocol4 to provide a mixture of diastereomers (3) at the 2-position in 93% yield and in a ratio of ca. 2:1.

In this alkylation, the selectivity was found to be somewhat compromised, and the isomers could not be
separated by column chromatography. In order to separate the diastereoisomeric mixture, the silyl group
of 3 was removed upon treatment with tetrabutylammonium fluoride (TBAF) to give a hydroxyl-ester (4)
in 97% yield. Alkaline hydrolysis of 4 afforded the corresponding acid, which, without further
purification, was reacted with N,N’-dicyclohexylcarbodiimide (DCC) in CHCl3 in the presence of
N,N-dimethylaminopyridine (DMAP) by following Nagumo’s procedure4 to furnish the lactone (5) in
50% yield from 4. Methanolysis of 5 provided pure hydroxyl-ester (6) in 98% yield.
Swern oxidation of 6 in the usual manner afforded the ketone (7), which was treated with hydroxylamine
hydrochloride in EtOH in the presence of pyridine to give the oxime (8) as a mixture of E and Z-isomers
in 88% yield and in a ratio of ca. 1:1. Since difficulties were encountered in separating E and Z-isomers
as pure forms, we decided to use a mixture of the oximes in the following fragmentation. Tosylation of 8
with tosyl chloride in the presence of DMAP and diisopropylethylamine (DIPEA) gave oxime tosylates
(9) as E and Z-isomers. (Scheme 2)
With the desired compound 9 in hand, a study was carried out to determine the best conditions for
Beckmann fragmentation reaction, and the results obtained are summarized in Table 1.
Table 1. Beckmann fragmentation of oxime tosylates (9)
OTs
H
N
N
NC
H2N
O
OBn
OBn
acid
OBn
+
CO2Me
N
N
H
CO2Me
CO2Me
Boc
9
10
11
b
b
Entry
acida
temp. (°C)
time (h)
(%)
10
11
(%)
1
2
3
4
5
TFA
- 20
0
72
36
12
36
24
18c
TFA
70
TFA
36
rt
27
ZnBr2
ZnBr2
0
5c
12
rt
52
a15 equimolar amounts of TFA and 6 equimolar amounts of ZnBr2 were employed.
b Isolated yield. cMost of the starting material was recovered.
Based on consideration of the previously established heteroatom-assisted Beckmann fragmentation,3 the
desired bond cleavage reaction would be concomitant with removal of the Boc group on the nitrogen
atom. Thus, the tosylate (9) was exposed to trifluoroacetic acid (TFA) at -20 °C for 72 h; however, the
desired product (10) was isolated only in 18% yield together with the recovered starting material (entry 1).

When the reaction was carried out at 0 °C for 36 h, the yield was increased to 70% (entry 2). Interestingly,
a higher temperature for the reaction brought about Beckmann rearrangement prior to Beckmann
fragmentation, probably due to facile isomerization between E and Z-isomers under these reaction
conditions (entry 3). When removal of the Boc group was attempted with the use of Lewis acid, the
rearrangement product (11) was always generated preferentially (entries 4 and 5). The reason for the
formation of the rearrangement product as the major product by the use of zinc bromide was not clear;
however, zinc metal might participate both with pyrrolidine nitrogen and oxime oxygen (or oxime
nitrogen) to accelerate isomerization of the E-isomer to the Z-isomer, leading to the observed
rearrangement.
Although alkaline hydrolysis of the nitrile (10) with aqueous KOH solution was first attempted,8-11 the
desired di-acid or amide-acid could not be isolated under these reaction conditions. Similar hydrolysis
with hydrochloric acid gave the di-acid, which, without purification, was subjected to an esterification
with trimethylsilyldiazomethane,12 to give its dimethyl ester (12).
Scheme 3. Synthesis of dimethyl 2-(4-hydroxybenzyl)-L-aspartate (12)
In summary, we established
a
novel synthesis of an optically pure methyl
O-benzyl-2-(-cyanomethyl)-D-tyrosinate and dimethyl 2-(4-hydroxybenzyl)-L-aspartate employing
(2S,4R)-4-hydroxyproline as the starting chiral pool. This methodology will provide an alternative route
for the synthesis of -disubstituted -amino acid, and its further application is now under investigation
in our laboratory.
EXPERIMENTAL
Melting points were measured with a Yanagimoto MP apparatus and are uncorrected. IR spectra were
1
obtained using a JASCO FT/IR-4100 spectrophotometer. H- and 13C-NMR spectra were obtained on
13
BRUKER AV400 (1H-NMR: 400 MHz, C-NMR: 100 MHz) instrument for solutions in CDCl3 unless
otherwise noted, and chemical shifts are reported on the  scale from internal TMS. MS spectra were
measured with a JEOL JMS-600W spectrometer. Elemental analyses were performed on a Yanaco-MT5.
1-tert-Butyl 2-methyl (4S)-2-[4-(benzyloxy)benzyl-4-{[tert-butyl(dimethyl)silyl]oxy}-pyrrolidine-1,2-

dicarboxylate (3). To a stirred solution of 2 (1.0 g, 2.8 mmol) in THF (18 mL) was added LiHMDS (1.6
M THF solution, 3.5 mL, 1.6 M, 5.6 mmol) at 0 °C under argon, and the resulting mixture was stirred for
further 1 h at the same temperature. To this solution was added a solution of (4-benzyloxy)benzyl
chloride (1.6 g, 7.0 mmol) in THF (10 mL), and the whole was stirred for 5 h at 0 °C. The mixture was
treated with saturated aqueous NH4Cl solution, and extracted with AcOEt. The extract was washed with
brine and dried over Na2SO4. Evaporation of the solvent gave a residue, which was subjected to column
chromatography on silica gel. Elution with hexane:AcOEt (7:1, v/v) afforded the benzylated compound
(3) (1.44 g, 93%) as a mixture of diastereomers at the 2-position and Boc rotamers. IR  max: 1744 1611
cm-1; 1H-NMR  7.46-7.28 (m, 5H), 7.13-7.01 (m, 2H), 6.95-6.88 (m, 2H), 5.06-5.01 (m, 2H), 4.41-4.29
(m, 0.3H), 3.88-3.80 (m, 0.2H), 3.77-3.73 (m, 3H), 3.71-3.61 (m, 0.5H), 3.50-3.35 (m, 1H), 3.31-3.21 (m,
0.2H), 3.15-2.91 (m, 2.4H), 2.48 (dd, J = 7.8, 10.5 Hz, 0.2H), 2.40 (dd, J = 7.8, 10.5 Hz, 0.1H), 2.20-2.14
(m, 2.1H), 1.51 (s, 2.3H), 1.49 (s, 4.7H), 1.45 (s, 2H), 0.82 (s, 1H), 0.81 (s, 2H), 0.76 (s, 2.3H), 0.74 (s,
3.7H), 0.01 - -0.03 (m, 2H), -0.16 - -0.19 (m, 4H).; 13C-NMR  174.7, 174.6, 174.4, 158.0, 157.8, 157.6,
153.9, 153.2, 137.0, 137.0, 136.9, 132.1, 132.0, 131.4, 131.3, 129.6, 129.1, 128.6, 128.5, 128.5, 127.9,
127.9, 127.8, 127.4, 127.4, 127.3, 114.8, 114.6, 114.3, 80.49, 79.80, 69.98, 69.90, 68.23, 67.97, 67.73,
67.51, 67.25, 67.08, 67.00, 54.36, 54.14, 53.84, 52.23, 44.83, 43.90, 43.22, 42.23, 39.13, 38.57, 38.04,
28.30, 25.69, 17.95, 17.89, 17.84, -4.89, -4.95, -5.08, -5.18, -5.24, -5.27.; MS (EI): 555 (M+); HRMS
(EI): Calcd for : C31H45NO6Si: 555.3016, Found: 555.3029.
1-tert-Butyl 2-methyl (4S)-2-[4-(benzyloxy)benzyl-4-hydroxypyrrolidine-1,2-dicarboxylate (4). To a
stirred solution of 3 (3.36 g, 6.0 mmol) in THF (12 mL) was added TBAF (1.0 M THF solution, 7.3 mL,
7.3 mmol) at 0 °C, and the resulting mixture was stirred for further 3 h at the same temperature. After
removal of the solvent, the residue was purified by column chromatography on silica gel. Elution with
hexane:AcOEt (1:1, v/v) afforded the desilylated compound (4) (2.58 g, 97%) as a mixture of
1
diastereomers at the 2-position and Boc rotamers. IR  max: 3458, 1742, 1695 cm-1; H-NMR :
7.45-7.29 (m, 5H), 7.15-6.98 (m, 2H), 6.97-6.86 (m, 2H), 5.05-5.01 (m, 2H), 3.92-3.71 (m, 4.3H),
3.70-3.42 (m, 1.7H), 3.03 (d, J = 14.2 Hz, 0.2H), 3.02 (d, J = 14.2 Hz, 0.1H), 2.88 (d, J = 14.2 Hz, 0.4H),
2.84 (d, J = 14.2 Hz, 0.3H), 2.93-2.84 (m, 0.3H), 2.76 (dd, J = 4.4, 11.6 Hz, 0.4H), 2.61 (dd, J = 4.4, 11.6
13
Hz, 0.3H), 2.36-2.21 (m, 1H), 2.10-2.01 (m, 1H), 1.51 (s, 3H), 1.50 (s, 4H), 1.48 (s, 2H).; C-NMR :
176.5, 176.0, 174.7, 157.9, 157.8, 157.7, 154.0, 153.2, 136.9, 136.8, 132.2, 132.1, 131.8, 131.7, 128.5,
128.2, 127.9, 127.9, 127.4, 114.9, 114.8, 114.8, 114.5, 80.87, 80.26, 69.92, 69.65, 68.88, 68.35, 67.89,
67.63, 67.35, 67.28, 57.00, 56.45, 56.11, 55.58, 53.08, 52.84, 52.33, 43.46, 43.19, 42.69, 42.04, 38.59,
38.15, 37.46, 36.73, 28.38, 28.33.; MS (EI): 441 (M+); HRMS (EI): Calcd for : C25H31NO6: 441.2151,
Found: 441.2124.

tert-Butyl (1S,4S)-4-[4-(benzyloxy)benzyl]-3-oxo-2-oxa-5-azabicyclo[2.2.1]heptane-5-carboxylate (5).
A solution of 4 (6.5 g, 14.7 mmol) in MeOH (75 mL) and 2.0 M NaOH solution (75 mL, 147 mmol) was
heated at reflux for 4 h. The solution was acidified with 10% HCl solution and extracted with AcOEt. The
extract was washed with brine and dried over Na2SO4. Evaporation of the solvent gave a crude acid,
which, without further purification, was used in the next step. To a stirred solution of the crude acid (6.3
g) in CHCl3 (1.5 L) were added DMAP (180 mg, 1.5 mmol) and DCC (6.1 g, 29.5 mmol) at 0 °C, and the
whole was stirred for 10 h at the same temperature. The mixture was treated with 1N HCl and extracted
with CHCl3. The extract was washed with brine and dried over Na2SO4. Evaporation of the solvent gave a
residue, which was subjected to column chromatography on silica gel. Elution with hexane:AcOEt (5:1,
v/v) afforded the lactone (5) (3.0 g, 50%) as colorless solid; mp 130-131 °C; []D +154.3 (c 0.99, CHCl3);
IR  max: 1790, 1703 cm-1; 1H-NMR : 7.45-7.30 (m, 5H), 7.21-7.16 (m, 2H), 6.92-6.87 (m, 2H), 5.03 (s,
13
2H), 4.83 (d, J = 1.7 Hz, 1H), 3.62-3.52 (m, 4H), 1.88 (d, J = 10.8 Hz, 1H), 1.50 (s, 9H).; C-NMR :
171.8, 157.7, 155.2, 136.9, 131.4, 128.8, 128.1, 128.0, 127.9, 127.5, 115.1, 114.8, 81.60, 74.88, 69.99,
69.93, 68.47, 53.71, 43.42, 32.55, 28.28.; MS (EI): 409 (M+); HRMS (EI): Calcd for C24H27NO5:
409.1889. Found: 409.1881, Anal. Calcd for C24H27NO5: C, 70.40; H, 6.65; N, 3.42, Found: C, 70.12; H,
6.68; N, 3.41.
1-tert-Butyl 2-methyl (2S,4S)-[4-(benzyloxy)benzyl]-4-hydroxypyrrolidine-1,2-dicarboxylate (6). To
a solution of 5 (7.1 g, 17.3 mmol) in MeOH (170 mL) was added NaOMe (28% MeOH solution, 5.3 mL,
26.0 mmol) at rt and the mixture was stirred for 1 h at the same temperature. The mixture was treated
with saturated aqueous NH4Cl solution and extracted with AcOEt. The extract was washed with brine and
dried over Na2SO4. Evaporation of the solvent gave a residue, which was subjected to column
chromatography on silica gel. Elution with hexane:AcOEt (2:1, v/v) afforded the hydroxyl-ester (6) (7.5 g,
98%) as colorless solid; mp 103-104 °C; []D +235.1 (c 1.00, CHCl3); IR max: 3449, 1742, 1695 cm-1;
1H-NMR : 7.45-7.29 (m, 5H), 7.05-6.98 (m, 2H), 6.93-6.87 (m, 2H), 5.03 (d, J = 2.8 Hz, 2H), 3.84 (s,
1.5H), 3.83 (s, 1.5H), 3.76 (d, J = 14.0 Hz, 1H), 3.66-3.44 (m, 2H), 2.88 (d, J = 14.3 Hz, 0.5H), 2.84 (d, J
= 14.3 Hz, 0.5H), 2.76 (dd, J = 11.6 Hz, 0.5H), 2.61 (dd, J = 11.6 Hz, 0.5H), 2.32-2.22 (m, 1H), 2.10-2.00
13
(m, 1H), 1.51 (s, 4.5H), 1.50 (s, 4.5H). One proton (OH) was not observed.; C-NMR : 176.5, 176.0,
158.0, 157.7, 154.0, 153.1, 136.9, 136.8, 131.8, 131.7, 128.5, 128.2, 127.9, 127.9, 127.4, 114.8, 114.5,
80.86, 80.25, 69.91, 69.64, 68.88, 67.34, 67.27, 57.00, 56.45, 53.08, 52.84, 43.19, 42.04, 38.15, 36.73,
28.38.; MS (CI): 441 (M+); HRMS (CI): Calcd for C25H31NO6: 441.2151, Found: 441.2159, Anal. Calcd
for C25H31NO6: C, 68.01; H, 7.08; N, 3.17, Found: C, 68.04; H, 7.21; N, 3.22.
1-tert-Butyl 2-methyl (2S)-2-[4-(benzyloxy)benzyl]-4-oxopyrrolidine-1,2-dicarboxylate (7). To a
stirred solution of oxalyl chloride (1.5 mL, 17.0 mmol) in CH2Cl2 (10 mL) was added a solution of

DMSO (1.9 mL, 27.2 mmol) in CH2Cl2 (10 mL) at -78 °C, and the resulting mixture was stirred for 15
min at the same temperature. To this solution was added a solution of 6 (3.0 g, 6.8 mmol) in CH2Cl2 (14
mL) and the whole was stirred for 30 min. Et3N (7.5 mL, 54.4 mmol) was then added to the mixture and
the whole mixture was stirred for further 30 min at the same temperature. The mixture was treated with
water and extracted with CHCl3. The extract was washed with brine and dried over Na2SO4. Evaporation
of the solvent gave a residue, which was subjected to column chromatography on silica gel. Elution with
hexane:AcOEt (7:1, v/v) afforded the ketone (7) (2.6 g, 86%) as a colorless oil. []D +119.1 (c 0.99,
CHCl3); IR  max: 1767, 1747, 1701 cm-1; 1H-NMR : 7.44-7.29 (m, 5H), 7.01 (d, J = 8.0 Hz, 2H), 6.89
(d, J = 8.6 Hz, 2H), 5.02 (s, 2H), 3.88-3.56 (m, 2H), 3.80 (s, 3H), 3.13 (d, J = 19.2 Hz, 0.5H), 3.05-2.95
(m, 1.5H), 2.84-2.69 (m, 2H), 1.52 (s, 4.5H), 1.51 (s, 4.5H).; 13C-NMR : 207.0, 206.0, 173.4, 158.1,
152.9, 136.7, 131.7, 128.5, 127.9, 127.5, 127.3, 126.7, 115.2, 115.0, 81.75, 81.01, 69.93, 66.23, 54.39,
54.27, 52.69, 47.05, 46.59, 39.29, 38.05, 28.28.; MS (EI): 439 (M+); HRMS (EI): Calcd for C25H29NO6:
439.1995, Found: 439.1989.
1-tert-Butyl
2-methyl
(2S,4E/Z)-2-[4-(benzyloxy)benzyl]-4-(hydroxyimino)pyrrolidine-1,2-
dicarboxylate (8). To a stirred solution of 7 (2.6 g, 5.9 mmol) in pyridine (24 mL) and EtOH (8 mL) was
added hydroxylamine hydrochloride (2.0 g, 29.4 mmol) and the resulting solution was heated at 60 °C for
1 h. The mixture was treated with water and extracted with AcOEt. The extract was washed with brine
and dried over Na2SO4. Evaporation of the solvent gave a residue, which was subjected to column
chromatography on silica gel. Elution with hexane:AcOEt (2:1, v/v) afforded the oxime (8) (2.4 g, 88%)
as a mixture of E/Z-isomers (ca. 1:1). This mixture was separated by careful column chromatography on
silica gel to give E and Z-isomer, respectively. However, the stereochemistry of the isomer was not able
to determine at this stage.
1
E or Z-isomer; mp 51-53 °C; []D +9.1 (c 1.00, CHCl3); IR  max: 3380, 1745, 1698 cm-1; H-NMR :
7.45-7.29 (m, 5H), 7.03 (t, J = 7.8 Hz, 2H), 6.87 (d, J = 8.5 Hz, 2H), 5.02 (s, 2H), 4.13 (d, J = 15.8 Hz,
0.6H), 4.04 (d, J = 15.8 Hz, 0.4H), 3.78 (s, 3H), 3.80-3.71 (m, 0.4H), 3.54 (d, J = 14.2 Hz, 0.6H), 3.48 (d,
J = 16.0 Hz, 0.6H), 3.39 (d, J = 16.0 Hz, 0.4H), 3.07 (d, J = 13.2 Hz, 0.4H), 3.02 (d, J = 13.2 Hz, 0.6H),
2.98 (d, J = 14.2 Hz, 1H), 2.88 (d, J = 18.4 Hz, 1H), 1.50 (s, 9H). One proton (OH) was not observed.;
13C-NMR : 173.8, 157.9, 157.8, 156.8, 155.7, 153.7, 136.9, 131.5, 128.5, 127.9, 127.8, 127.5, 127.2,
114.9, 114.7, 81.43, 80.66, 69.86, 67.85, 67.71, 52.62, 52.53, 49.69, 39.24, 37.98, 36.31, 35.55, 28.29;
MS (EI): 454 (M+); HRMS (EI): Calcd for C25H30N2O6: 454.2104, Found: 454.2111.
1
E or Z-isomer; mp 49-51 °C; []D +129.8 (c 0.99, CHCl3); IR  max: 3381, 1745, 1699 cm-1; H-NMR
: 7.74 (s, 0.5H), 7.65 (s, 0.5H), 7.44-7.28 (m, 5H), 7.03 (t, J = 8.2 Hz, 2H), 6.87 (d, J = 8.6 Hz, 2H), 5.02
(s, 2H), 4.20 (d, J = 17.8 Hz, 0.5H), 4.12 (d, J = 17.8 Hz, 0.5H), 3.80-3.73 (m, 0.5H), 3.77 (s, 3H), 3.66 (d,

J = 17.8 Hz, 0.5H), 3.55 (d, J = 16.0 Hz, 1H), 3.00 (d, J = 14.2 Hz, 1H), 2.92-2.80 (m, 2H), 1.51 (s, 4.5H),
1.50 (s, 4.5H). One proton (OH) was not observed.; 13C-NMR : 173.7, 157.8, 157.7, 157.0, 156.0, 154.0,
153.2, 136.8, 131.6, 131.6, 128.4, 127.8, 127.7, 127.3, 127.2, 114.9, 114.6, 81.32, 80.59, 69.78, 67.22,
66.98, 52.59, 52.48, 47.80, 38.99, 38.79, 37.91, 37.73, 28.21.; MS (EI): 454 (M+); HRMS (EI): Calcd for
C25H30N2O6: 454.2104, Found: 454.2111.
1-tert-Butyl
2-methyl
(2S,4E/Z)-2-[4-(benzyloxy)benzyl]-4-(tosyloxyimino)pyrrolidine-1,2-
dicarboxylate (9). To a stirred solution of 8 (3.0 g, 6.6 mmol) in CHCl3 (70 mL) were successively added
DIPEA (2.3 mL, 13.2 mmol), TsCl (2.5 g, 13.2 mmol), and DMAP (80 mg, 0.7 mmol) at 0 °C, and the
resulting mixture was stirred for further 6 h at the same temperature. The mixture was treated with water
and extracted with CHCl3. The extract was washed with brine and dried over Na2SO4. Evaporation of the
solvent gave a residue, which was subjected to column chromatography on silica gel. Elution with
hexane:AcOEt (9:1, v/v) afforded the oxime tosylate (9) (3.9g, 96%) as a mixture of E/Z-isomers (ca. 1:1).
This mixture was separated by careful column chromatography on silica gel.
E or Z-isomer; []D -23.7 (c 0.99, CHCl3); IR max: 1747, 1701 cm-1; 1H-NMR : 7.76 (d, J = 8.0 Hz,
2H), 7.45-7.28 (m, 7H), 7.00-6.95 (m, 2H), 6.79 (d, J = 8.6 Hz, 2H), 4.99 (s, 2H), 4.14 (d, J = 17.2 Hz,
0.5H), 4.06 (d, J = 17.2 Hz, 0.5H), 3.75 (s, 3H), 3.78-3.68 (m, 0.5H), 3.51 (d, J = 14.4 Hz, 0.5H), 3.43 (d,
J = 17.2 Hz, 0.5H), 3.35 (d, J = 17.2 Hz, 0.5H), 3.13 (dd, J = 6.8, 18.8 Hz, 1H), 3.03-2.95 (m, 1H), 2.94
13
(d, J = 14.2 Hz, 1H), 2.36 (s, 3H), 1.47 (s, 9H).; C-NMR : 172.7, 166.0, 165.1, 158.0, 157.9, 153.2,
152.5, 145.2, 136.7, 132.1, 131.3, 129.6, 128.6, 128.4, 127.9, 127.5, 127.1, 126.5, 115.1, 114.9, 81.72,
81.00, 69.84, 67.79, 67.60, 52.71, 52.63, 49.59, 39.04, 38.04, 37.80, 37.27, 28.15, 21.50.; HRMS (ESI):
Calcd for C32H36N2O8S: 631.2090, Found: 631.2061.
1
E or Z-isomer; []D +53.4 (c 0.99, CHCl3); IR  max: 1747, 1701 cm-1; H-NMR : 7.08-7.71 (m, 2H),
7.47-7.24 (m, 7H), 6.96 (d, J = 8.0 Hz, 2H), 6.83-6.75 (m, 2H), 5.02 (s, 2H), 4.24 (d, J = 18.8 Hz, 0.4H),
4.15 (d, J = 18.8 Hz, 0.6H), 3.79-3.69 (m, 0.6H), 3.73 (s, 3H), 3.68-3.46 (m, 0.6H), 3.02-2.90 (m, 3H),
13
2.40 (s, 3H), 1.50 (s, 9H).; C-NMR : 173.0, 166.5, 165.6, 158.1, 153.6, 152.9, 145.3, 136.9, 132.3,
131.7, 129.8, 128.7, 128.6, 128.0, 127.6, 127.1, 126.6, 115.1, 114.9, 81.87, 81.35, 70.05, 67.86, 67.66,
67.43, 52.87, 49.11, 39.27, 39.08, 38.50, 37.88, 28.35, 21.71.; HRMS (ESI): Calcd for C32H36N2O8S:
631.2090, Found: 631.2083.
Methyl O-benzyl-2-(-cyanomethyl)-D-tyrosinate (10). To a stirred solution of 9 (3.5 g, 5.8 mmol) in
CH2Cl2 (60 mL) was added TFA (6.4 mL, 86.3 mmol) at 0 °C, and the resulting mixture was stirred for
further 24 h at the same temperature. The mixture was treated with saturated aqueous NaHCO3 solution
and extracted with CHCl3. The extract was washed with brine and dried over Na2SO4. Evaporation of the
solvent gave a residue, which was subjected to column chromatography on silica gel. Elution with

hexane:AcOEt (1:1, v/v) afforded the cyanide (10) (1.3 g, 70%) as a pale yellowish oil. []D -24.1 (c 1.00,
1
CHCl3); IR max: 3379, 2249, 1738 cm-1; H-NMR : 7.44-7.29 (m, 5H), 7.07-7.02 (m, 2H), 6.94-6.88
(m, 2H), 5.03 (s, 2H), 3.73 (s, 3H), 3.05 (d, J = 13.6 Hz, 1H), 2.91 (d, J = 13.6 Hz, 1H), 2.77 (d, J = 16.5
13
Hz, 1H), 2.63 (d, J = 16.5 Hz, 1H). Two protons (NH) were not observed.; C-NMR : 173.8, 158.2,
136.7, 130.7, 128.5, 127.9, 127.4, 126.5, 116.9, 114.9, 69.86, 60.27, 52.70, 44.24, 27.80.; MS (CI): 325
(M+H); HRMS (EI): Calcd for C19H21N2O3: 325.1552, Found: 325.1565.
Methyl (2S)-2-[4-(benzyloxy)benzyl]-5-oxo-piperadine-2-carboxylate (11). To a stirred solution of 9
(120 mg, 0.2 mmol) in CH2Cl2 (2 mL) was added ZnBr2 (260 mg, 1.2 mmol) at rt and the resulting
mixture was stirred for further 24 h at the same temperature. The mixture was treated with saturated
aqueous NaHCO3 solution and extracted with CHCl3. The extract was washed with brine and dried over
Na2SO4. Evaporation of the solvent gave a residue, which was subjected to column chromatography on
silica gel. Elution with hexane:AcOEt (1:1, v/v) afforded the amide (11) (36 mg, 52%) as a pale yellowish
1
oil. []D +27.8 (c 1.01, CHCl3); IR  max: 3351, 1756, 1732 cm-1; H-NMR : 7.45-7.30 (m, 5H),
7.10-7.05 (m, 2H), 6.94-6.88 (m, 2H), 5.04 (s, 2H), 3.70 (s, 3H), 3.37 (s, 2H), 3.18 (d, J = 13.5 Hz, 1H),
2.96 (d, J = 13.5 Hz, 1H), 2.78 (d, J = 18.2 Hz, 1H), 2.42 (d, J = 18.2 Hz, 1H). Two protons (NH) were
13
not observed; C-NMR : 213.4, 175.0, 158.0, 136.9, 130.8, 128.6, 129.0, 128.0, 127.5, 114.8, 69.96,
68.26, 53.74, 52.48, 45.79, 43.91.; MS (CI): 354 (M+); HRMS (EI): Calcd for C20H22N2O4: 354.1580,
Found: 354.1556. Further elution with the same solvent system furnished the fragmentation product (10)
(0.22 g, 12%).
Dimethyl 2-(4-hydroxybenzyl)-L-aspartate (12). A solution of 10 (200 mg, 0.62 mmol) in EtOH (1 mL)
and conc. HCl (10 mL) was heated at 100 °C using a sealed tube for 48 h. After removal of EtOH and
water, the residue was dissolved into MeOH (6 mL). To this solution was added TMSCHN2 (2M ether
solution, 1.6 mL, 3.1 mmol) at 0 °C and the resulting mixture was stirred for further 6 h at the same
temperature. The mixture was treated with AcOH (2 mL) and then saturated aqueous NaHCO3 solution,
and extracted with AcOEt. The extract was washed with brine and dried over Na2SO4. Evaporation of the
solvent gave a residue, which was subjected to column chromatography on silica gel. Elution with
hexane:AcOEt (4:1, v/v) afforded the diester (12) (90 mg, 55%) as a pale yellowish oil. []D +16.3 (c
0.80, CHCl3); IR  max: 3355, 3297, 1732 cm-1; 1H-NMR : 6.84 (d, J = 8.4 Hz, 2H), 6.62 (d, J = 8.4 Hz,
2H), 4.19 (br s, 2H), 3.61 (s, 3H), 3.58 (s, 3H), 3.02 (d, J = 17.0 Hz, 1H), 2.89 (d, J = 13.5 Hz, 1H), 2.71
(d, J = 13.5 Hz, 1H), 2.57 (d, J = 17.0 Hz, 1H). One proton (OH) was not observed.; 13C-NMR : 175.8,
171.9, 155.2, 131.0, 125.5, 115.6, 60.06, 52.40, 51.85, 44.80, 42.83.; MS (EI): 267 (M+); HRMS (EI):
Calcd for C13H17NO5: 267.1107, Found: 267.1113.

ACKNOWLEDGEMENTS
This research was supported financially in part by a grant for the Open Research Center Project and a
Grant-in-Aid from the Ministry of Education, Culture, Sports, Science and Technology of Japan.
REFERENCES
†
This paper is dedicated to Professor Ei-ichi Negishi on the occasion of his 77th birthday.
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