Highly enantioselective cyclocarbonylation of allylic alcohols catalyzed by novel-Pd-1,4-bisphosphine complexes [7]

Full text of DOI:10.1021/ja991547k

7708
J. Am. Chem. Soc. 1999, 121, 7708-7709
Highly Enantioselective Cyclocarbonylation of
Allylic Alcohols Catalyzed by Novel
Pd-1,4-bisphosphine Complexes
Scheme 1
Ping Cao and Xumu Zhang*
Department of Chemistry
The PennsylVania State UniVersity
UniVersity Park, PennsylVania 16802
ReceiVed May 7, 1999
Transition metal-catalyzed carbonylation reactions are funda-
mentally important organic transformations.1 Despite the great
potential of asymmetric carbonylation reactions and the extensive
effort devoted to this reaction during the last several decades,4
only moderate success (<90% ee) has been achieved, and the
development of efficient asymmetric carbonylations is still viewed
as one of the most challenging problems in asymmetric catalysis.
We have been interested in exploring the asymmetric cyclocar-
bonylation of allylic alcohols for the synthesis of chiral γ-buty-
rolactones, important functionalities in many natural products and
biologically active molecules.5 Alper et al. have extensively
studied Pd-catalyzed cyclocarbonylation of allylic alcohols and
developed the first enantioselective variant of this reaction using
commercially available chiral bisphosphine ligands albeit with
,3
Figure 1. BICP and Xyl-BICP ligands.
which significantly increases the scope and synthetic utility of
the asymmetric carbonylation reaction.
Recently, we have achieved high enantioselectivity in a number
of Rh-BICP and Ru-BICP catalyzed asymmetric hydrogenation
7
reactions. These results demonstrated that the BICP ligand is an
excellent chiral motif for group VIII transition metal-catalyzed
reactions. To optimize the steric and electronic properties of BICP,
we have also synthesized a modified BICP ligand by substituting
the phenyl groups by m-xylene [(2R, 2′R)-bis[bis-(3,5-dimeth-
ylphenyl)phosphino]-(1R,1′R)-dicyclopentane, Xyl-BICP, Figure
6
moderate ee’s. The asymmetric reaction is, however, restricted
to â-substituted allylic alcohols with dialkyl substitution at the R
position (geminal dialkyl effect) (1 to 2, Scheme 1). Herein we
report the highly enantioselective cyclocarbonylation of allylic
alcohols 1 catalyzed by Pd complexes with BICP and related
ligands developed in our lab (Figure 1). Another major advance
in this study is the development of the first highly enantioselective
cyclocarbonylation of â,γ-substituted allylic alcohols 3 lacking
geminal dialkyl substituents at the R position (3 to 4, Scheme 1),
8
6e
9
1]. Alper and van Leeuwen have studied the rate of CO
insertion into a Pd-alkyl bond and found that the rate decreases
in the order: 1,4-bisphosphine > 1,3-bisphosphine . 1,2-
bisphosphine. The high catalytic reactivity the Pd-catalyzed
carbonylation with a 1,4-bisphosphine ligand is associated with
a relatively flexible ligand-metal seven-membered ring chelate.
Since BICP is one of the most effective chiral 1,4-bisphosphines,
we chose to evaluate this ligand as it might meet the two primary
requirements for achieving high enantioselectivity and activity
in Pd-catalyzed cyclocarbonylation reactions: (1) conformational
rigidity of Pd-bisphosphine complexes conducive to chiral
induction and (2) a relatively flexible seven-membered ligand-
metal chelate favorable for rapid CO insertion.
(
1) (a) Colquhoun, H. M.; Thompson D. J.; Twigg, M. V. Carbonylation:
Direct Synthesis of Carbonyl Compounds; Plenum Press: New York, 1991.
b) Stille, J. K. In ComprehesiVe Organic Organic Synthesis; Trost, B. M.,
(
Fleming, I., Eds.; Pergamon Press: New York, 1991; Vol. 4, p 913. (c) Ojima,
I.; Tzamarioudaki, M.; Li, Z.; Donovan, R. J. Chem. ReV. 1996, 96, 635. (d)
Applied Homogeneous Catalysis with Organometallic Compounds: A Com-
prehensiVe Handbook in Two Volumes; Cornils, B., Herrmann, W. A., Eds.;
VCH: New York, 1996; p 27. (e) Ungv a´ ry, F. Coord. Chem. ReV. 1998, 170,
We selected 3,3-dimethyl-2-phenyl propenol (1a) as the initial
substrate for study. Several experiments have been conducted to
2
45.
2) Acetic Acid and its DeriVatiVes; Agreda, V. H., Zoeller, J. R., Eds.;
Marcel Dekker: New York, 1993.
3) (a) Elango, V.; Murphy, M. A.; Moss, G. L.; Smith, B. L.; Davenport,
(
identify CH
psi, ratio of CO/H
Pd-catalyst(Table 1). The Pd-BICP catalyst was prepared in situ
from Pd (dba) and (R,R)-BICP. Under these conditions, cyclo-
Cl
2 2
under a CO/H
2
atmosphere (total pressure ) 800
(
) 1:1) at 80 °C with 1 mol % of
2
K. G.; Mott, G. N. (Hoechst Celanese Corporation). EP 00.284.310, 1988;
Chem. Abstr. 1989, 110, 153916t. (b) Rittner, S.; Schmidt, A.; Wheeler, L.
O.; Moss, G. L.; Zey, E. G. (Hoechst AG). EP 00.326.027 1989; Chem. Abstr.
2
3
1
990, 112, 35448k. (c) Armor, J. N. Appl. Catal. 1991, 78, 141.
4) Reviews: (a) Agbossou, F.; Carpentier, J.-F.; Mortreux, A. Chem. ReV.
995, 95, 2485. (b) Gladiali, S.; Bayon, J. C.; Claver, C. Tetrahedron:
carbonylation of 1a gave product 2a in 95%ee (entry 1). When
Xyl-BICP was examined under the same reaction conditions,
lactone 2a was generated in 95% ee and 87% yield (entry 2). To
the best of our knowledge, this is the highest enantioselectivity
(
1
Asymmetry 1995, 6, 1453. (c) Consiglio, G. In Catalytic Asymmetric Synthesis;
Ojima, I., Ed.; VCH Publishers: New York, 1993; p 273. Selected recent
papers: (d) Nozaki, K.; Itoi, Y.; Shibahara, F.; Shirakawa, E.; Ohta, T.; Takaya,
H.; Hiyama, T. J. Am. Chem. Soc. 1998, 120, 4051. (e) Nozaki, K.; Sakai,
N.; Nanno, T.; Higashijima, T.; Mano, S.; Horiuchi, T.; Takaya, H. J. Am.
Chem. Soc. 1997, 119, 4413. (f) Babin, J. E.; Whiteker, G. T. (Union Carbide
Corp.). W.O. 93/03839, U.S. Patent 911518, 1992; Chem Abstr. 1993, 119,
reported to date for the cyclocarbonylation of 2-methyl-3-phenyl-
-buten-2-ol. In a related study, Alper et al.6 reported an 81%
e
3
ee for cyclocarbonylation of 1a using a Pd-BPPM catalyst,
whereas 45% ee and 31% ee were obtained with Pd-DIOP and
Pd-BINAP catalysts, respectively. No cyclocarbonylation of 1a
occurred when DuPhos and CHIRAPHOS were used as the chiral
ligands. Slow CO insertion into a rigid five-membered ring Pd-
ligand complex was proposed as a possible reason for this lack
of reactivity.6
1
59872h. (g) Buisman, G. J. H.; Vos, E. J.; Kamer, P. C. J.; van Leeuwen, P.
W. N. M. J. Chem. Soc., Dalton Trans. 1995, 409. (h) Stanley, G. In Catalysis
of Organic Reactions; Scaros, M. G.; Prunier, M. L., Eds.; Marcel Dekker:
New York, 1995; p 363. (i) Naili, S.; Carpentier, J.-F.; Agbossou, F.; Mortreux,
A.; Nowogrocki, G. Wignacourt, J.-P. Organometallics 1995, 14, 401. (j)
RajanBabu, T. V.; Ayers, T. A. Tetrahedron Lett. 1994, 35, 4295. (k) Stille,
J. K.; Su, H.; Brechot. P.; Parrinello, G.; Hegedus, L. S. Organometallics
e,9
1
991, 10, 1183.
(
5) (a) Nakanishi, K.; Goto, T.; Ito, S.; Nozoe, S. Natural Product
(7) (a) Zhu, G.; Cao, P.; Jiang, Q.; Zhang, X. J. Am. Chem. Soc. 1997,
119, 1799. (b) Zhu, G.; Casalnuovo, A. L.; Zhang, X. J. Org. Chem. 1998,
63, 8100. (c) Zhu, G.; Zhang, X. J. Org. Chem. 1998, 63, 9590. (d) Cao, P.;
Zhang, X. J. Org. Chem. 1999, 64, 2127.
Chemistry; Kodansha: Tokyo, 1974; Vols. I-III. (b) Dictionary of Natural
Products, 1st ed.; Buckingham, J., Ed.; Chapman & Hall: New York. 1994.
(6) (a) Alper, H.; Leonard, D. Tetrahedron Lett. 1985, 26, 5639. (b) Alper,
H.; Hamel, N. J. Chem. Soc., Chem. Commun. 1990, 135. (c) El Ali, B.; Alper,
H.; J. Org. Chem. 1991, 56, 5357. (d) El Ali, B.; Okuro, K.; Vasapollo, G.;
Alper, H. J. Am. Chem. Soc. 1996, 118, 4264. (e) Yu, W.; Bensimon, C.;
Alper, H. Chem. Eur. J. 1997, 3, 417. (f) Brunner, M.; Alper, H. J. Org.
Chem. 1997, 62, 7565.
(8) Zhu, G.; Zhang, X. Synlett, submitted for publication.
(9) (a) Dekker, G. P. C. M.; Elsevier, C. J.; Vrieze, K.; van Leeuwen, P.
W. N. M. Organometallics 1992, 11, 1598. (b) Dekker, G. P. C. M.; Elsevier,
C. J.; Vrieze, K.; van Leeuwen, P. W. N. M. J. Organomet. Chem. 1992,
430, 357.
1
0.1021/ja991547k CCC: $18.00 © 1999 American Chemical Society
Published on Web 08/10/1999

Communications to the Editor
J. Am. Chem. Soc., Vol. 121, No. 33, 1999 7709
Table 1. Enantioselective Cyclocarbonylation of Geminally
Table 2. Palladium-Catalyzed Enantioselective Cyclocarbonylation
Disubstituted Allylic Alcoholsa
of Allylic Alcoholsa
a
The reaction was complete at 80 °C under an initial total hydrogen
and carbon monoxide pressure of 800 psi (CO/H
2
) 1/1) for 24 h using
2 2 2
ClCH CH Cl as solvent. Substrate (0.25 mmol, 0.05M/Pd(OAc) /Ligand
b
a
The reaction was carried out at 80 °C under an initial total pressure
1:0.04:0.044. The ee was determined by GC. c The reaction was
)
of 800 psi (CO/H
M)/Pd (dba) /ligand ) 1:0.005:0.011]. The ee’s obtained were de-
c
2
) 1/1) for 24 h in CH Cl [substrate (1 mmol, 0.1
2 2
run under 60 °C.
b
2
3
termined by chiral GC. The absolute configuration was assigned by
1), cyclocarbonylation of an array of allylic substrates 3 gave
chiral γ-butyrolactones 4 in good to excellent enantioselectivities
d
comparison of the optical rotation with reported data. Sign of the
optical rotation.
(up to 98% ee) (Table 2).
In general, introduction of aromatic substituents at the â or γ
We have carried out cyclocarbonylation of various aliphatic
and aromatic unsaturated allylic alcohols catalyzed by Pd-BICP
and Pd-Xyl-BICP complexes under the optimal reaction condi-
tions (Table 1). In general, enantioselectivity in the cyclocarbo-
nylation of several of the allylic alcohols with the Pd-Xyl-BICP
catalyst is slightly higher than those obtained with the Pd-BICP
complex (entries 4 and 8). Overall, asymmetric cyclocarbonylation
of allylic alcohols containing an aromatic subsitituent gave chiral
γ-butyrolactones in high enantioselectivity and good yields
position of allylic alcohols enhances the enantioselectivity (entries
1-6 vs entry 7). The lactonization of the allylic alcohols 3 likely
proceeds through cis Pd-H migratory insertion to the allylic Cd
C bond followed by CO insertion into the transient Pd-C bond
to give trans chiral γ-butyrolactones. This trans stereochemistry
1
was confirmed by H NMR and 2D NOESY spectroscopic studies.
The observed stereospecificity probably results from cis addition
of the palladium hydride to the allylic CdC bond as proposed
by Alper. A notable advance emerging from these studies is the
asymmetric cyclocarbonylation of the six-membered ring allyli-
calcohol 3e using a Pd-BICP catalyst. At 80 °C, chiral γ-buty-
rolactone 4e was formed in 93% ee and 87% yield (entry 8). Upon
lowering the reaction temperature to 60 °C, up to 98% ee was
achieved (entry 9). A derivative (4f) of chiral γ-butyrolactone 4e
can be made by incorporating functional groups to the six-
membered ring of 3e (entry 10). Therefore, this cyclocarbonylation
method provides an efficient route to chiral six- and five-
membered fused ring compounds, which themselves are useful
building blocks for the synthesis of natural products and bioactive
molecules. For example, Weinreb’s recent synthesis of the
antitumor reagent papuamine used the chiral γ-butyrolactone 4e
as the starting material.11
In summary, we have developed a highly enantioselective Pd-
catalyzed asymmetric cyclocarbonylation of geminally disubsti-
tuted allylic alcohols and demonstrated the first highly enanti-
oselective cyclocarbonylation of â,γ-substituted allylic alcohols
lacking dialkyl substituents at the R position. These results
demonstrate that BICP is a unique chiral ligand for Pd-catalyzed
asymmetric carbonylation.
(entries 1-8). However, cyclocarbonylation of allylic alcohols
bearing aliphatic substituents at the R-position (1e, 1g) provides
γ-butyrolactones in only moderate to good enantiomeric excesses
(
entries 9 and 10). These results are consistent with Alper’s
7
observations with the Pd-BPPM catalyst. Furthermore, we have
confirmed Alper’s experimental results that the cyclocarbonylation
requires at least one substituent at the allylic position of the
alcohols (the geminal dialkyl effect). Alcohols such as 2-phenyl-
2-propen-1-ol, cinnamyl alcohol, and 2-pentene-1-ol do not give
the desired lactone products under the carbonylation conditions.
In an effort to expand the substrate scope and increas synthetic
utility of the carbonylation reaction, we explored asymmetric
palladium-catalyzed cyclocarbonylation of â,γ-substituted allylic
alcohols 3 without geminal dialkyl substituents at the R position
(Scheme 1). Although Alper et al. have recently developed a new
protocol for Pd-catalyzed cyclocarbonylation of â,γ-substituted
6f
allylic alcohols 3, there is no report on asymmetric modification
leading to products 4, trans R,â-Disubstituted chiral lactones are
key structural features of diverse lignans with cancer-protective
properties.10 Table 2 summarizes our experimental results of the
first Pd-catalyzed enantioselective cyclocarbonylation of â,γ-
substituted allylic alcohols 3. We chose (E)-2-methyl-cinnamyl
alcohol 3a as the substrate for initial optimization studies.
Acknowledgment. This work was supported by a Camille and Henry
Dreyfus New Faculty Award and Teacher-Scholar Award, an ONR Young
Investigator Award, and a DuPont Young Faculty Award.
Cyclocarbonylation reactions performed at 80 °C in ClCH
Cl using a catalyst prepared from 4 mol % Pd(OAc) and 4.4
mol % BICP gave the best enantioselectivity (entry 1, Table 2,
4% ee). Under these optimal reaction conditions for 3a (entry
2 2
CH -
Supporting Information Available: Spectroscopic data and experi-
mental details (PDF). This material is available free of charge via the
Internet at http://pubs.acs.org.
2
8
JA991547K
(
10) (a) Ward, R, S. Nat. Prod. Rep. 1999, 16, 75. (b) Ayres, D. C.; Loike,
(11) Boriziller, R. M.; Weinreb, S. M.; Parvez, M. J. Am. Chem. Soc. 1995,
117, 10905.
J. D. Lignans; Cambridge University Press: London, 1990.