Enantioselective synthesis of highly substituted furans by a copper(II)-catalyzed cycloisomerization-indole addition reaction

Article abstract of DOI:10.1021/ja202959n

A catalytic enantioselective reaction based on a copper(II) catalyst strictly containing chiral anionic ligands is described. In the present work, copper(II)-phosphate catalyst promotes the intramolecular heterocyclization of 2-(1-alkynyl)-2-alkene-1-ones

Full text of DOI:10.1021/ja202959n

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Enantioselective Synthesis of Highly Substituted Furans by a
Copper(II)-Catalyzed CycloisomerizationꢀIndole Addition Reaction
Vivek Rauniyar, Z. Jane Wang, Heather E. Burks, and F. Dean Toste*
Department of Chemistry, University of California, Berkeley, California 94720, United States
S Supporting Information
b
Scheme 1. Transition Metal Catalyzed Heterocyclization
ABSTRACT: A catalytic enantioselective reaction based on
a copper(II) catalyst strictly containing chiral anionic ligands is
described. In the present work, copper(II)ꢀphosphate
catalyst promotes the intramolecular heterocyclization of
2-(1-alkynyl)-2-alkene-1-ones and facilitates high levels
of enantioselectivity in the subsequent nucleophile attack.
Mechanistic studies suggest that formation of a copper(II)ꢀ
indole species is important for catalysis.
Table 1. Reaction Developmenta
nantioselective cycloisomerization reactions have emerged as
E
powerful methods for the asymmetric synthesis of a variety of
carbo- and heterocyclic structures.1 These reactions are most
commonly catalyzed by electrophilic late transition metal com-
plexes with chiral Lewis bases as ancilliary ligands that can
decrease the electrophilicity of the metal salt; as a result,
generation of a cationic variant of the ligated complex as the
active catalyst is often required. While this catalyst platform has
been successfully applied to rhodium,2 iridium,3 palladium,4
platinum,5 and gold6 catalyzed enantioselective cycloisomeriza-
tion reactions, its use in transformations promoted by silver and
copper is rare.7 Alternatively, unligated transition metal salts are
also effective catalysts for reactions triggered by the π-activation;
however, enantioselective cycloisomerization reactions employing
complexes lacking chiral L-type ligands remain scarce.8 Having
realized the potential of chiral phosphates as counterions in the
gold(I)-catalyzed enantioselective transformations,9 we envisioned
the utility of this motif in the form of an anionic X-type ligand for
electrophilic transition metal catalysis.10
Entry
Catalyst
Solvent
Temp
rt
%Convb
%eec
1
Ag(I)-4a
Ag(I)-4b
Ag(I)-4a
Cu(I)-4a
Cu(I)-4a
Cu(II)(4a)2
Cu(II)(4a)2
5
toluene
toluene
C6H5F
C6H5F
C6H5F
C6H5F
C6H5F
C6H5F
quant.
quant.
quant.
quant.
quant.
quant.
quant.
0%
72
72
74
80
80
80
91
n.d.
2
rt
3
rt
4
5d
rt
ꢀ15 °C
rt
6
7d
8
ꢀ15 °C
rt
For this study, we chose to explore the chiral binaphthol-
derived metal phosphates as potential catalysts for the asymmetric
addition of nucleophiles to the positively charged putative
intermediate generated from metal-catalyzed cycloisomerization
of 2-(1-alkynyl)-2-alkene-1-ones (Scheme 1).11,12 Based on the
importance of the indole scaffold in medicinal chemistry, we
began by examining the reaction of 2-(1-alkynyl)-2-alkene-
1-one (1) and indole (2) with Ag(I)ꢀbinaphthol phosphate
catalysts.10a,b When 1 and 2 (1.05 equiv) were treated with 5 mol
% Ag(4a) or Ag(4b), we observed a quantitative conversion to 3a
in promising levels of enantioselectivity (Table 1, entry 1ꢀ2).
We examined a panel of solvents for the reaction and found that
fluorobenzene enhanced the enantioselectivity of the reaction
without diminishing the product yield. However, when we
further examined the reaction with a variety of Ag(I)-binaphthol
phosphates (see Supporting Information for the complete list) at
a Conditions: 1.0 equiv of 1, 1.05 equiv of 2, 5 mol % MX or MX2, 0.2 M,
rt, 16 h. b Determined from crude reaction mixture. c Determined by
HPLC analysis. d Time = 50 h.
various temperatures, we were unable to optimize the reaction to
beyond 74% ee.
At this point, we hypothesized that changing the metal on the
catalyst may provide us with another avenue for exploration and
we began to examine the reaction with copper(I) and copper(II)
based complexes.10d,e The copper(II) salt was prepared via halide
abstraction from CuCl2•2H2O with 2.0 equiv of the correspond-
ing silver phosphate (4) and isolated as an air and moisture stable
Received: March 31, 2011
Published: May 11, 2011
r
2011 American Chemical Society
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dx.doi.org/10.1021/ja202959n J. Am. Chem. Soc. 2011, 133, 8486–8489
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Table 2. Substrate Scopea
Entry
R1
R2
R3
Product
% yieldb
%eec
1
Ph
H
H
H
H
H
H
H
H
H
H
H
H
H
H
H
H
H
H
H
H
H
H
H
H
Me
3a
3b
3c
3d
3e
3f
92
82
85
76
85
75
80
84
85
90
94
74
76
81
73
16
91
92
90
88
90
90
87
73
94
93
90
81
85
90
90
85
2
4-MeO-C6H4
3
4-Me-C6H4
4
4-F-C6H4
5
4-t-Bu-C6H4
Figure 1. Monitoring the reaction of 1 and 2 by 1H NMR. Series 1: 2.5
mol % Ag(I) added directly; Series 2: 5 mol % Cu(II) added after
incubation with 2; Series 3: 5 mol % Cu(II) added directly; Series 4: 5
mol % Cu(II) added after incubation with 1.
6
3-Me-C6H4
7
Cyclopentyl
3g
3h
3i
8
Bn
9
Cyclohexyl
10
11
12
13
14
15
16d
Ph
Ph
Ph
Ph
Ph
Ph
Ph
5-Br
6-Br
5-MeO
6-Me
5-Cl
5-F
3j
period (Figure 1, series 3). As both 1 and 2 are capable of binding
to Cu(II), we hypothesized that the induction period could be
due to catalyst coordination with 1 or 2 to generate the “active”
catalyst. When 1 and Cu(4a)2 were combined and stirred at
room temperature for 2 h and then added to a solution contain-
ing 2, a similar induction period was observed (Figure 1, series 4).
However, when a solution of 2 and Cu(4a)2 was prestirred for 2 h
and then added to 1, no induction period was observed and the
alkyne starting material was completely consumed in less than 3 h
(Figure 1, series 2).
3k
3l
3m
3n
3o
3p
H
a Conditions: 5 mol % Cu(4a)2 added to a solution of 1.0 equiv of 1
(0.2 M) and 1.05 equiv of 2, 50 h. b Isolated after chromatography.
c Determined by HPLC analysis. d Conducted at 5 °C.
Based on these observations, we posited that the active catalyst
for the reaction is a copper-indole complex and that formation of
this complex under catalytic conditions is responsible for the
induction period observed. The formation of this species can be
observed by high-resolution mass spectrometry and UVꢀvisible
spectroscopy. A UVꢀvisible spectrum of a solution of 2 and
Cu(4a)2 that was stirred at room temperature for 1 h shows a
new peak in the visible region at 373 nm, which is considerably
red-shifted from that of 2 or Cu(4a)2 (see Supporting Informa-
tion, Figure S2). High resolution mass spectrometry of the same
solution shows a new peak at 930.37 m/z, corresponding to a
complex with a copper/indole/phosphate ratio of 1:1:1. Under
the catalytic conditions, two copper-containing peaks are ob-
served at 814.30 and 1127.46 m/z by mass spectrometry,
corresponding to copper(II) monophosphate and copper(II)
monophosphate bound to both 1 and 2, respectively. Additionally,
the lack of nonlinear effects in the Cu(4a)2-catalyzed reaction of
1 and 2 is consistent with the presence of a single chiral
phosphate at the copper center during the enantiodetermining
step (see Supporting Information, Figure S3). Taken together,
these observations suggest that the copper-indole species is
important for catalysis. Though we have no direct evidence for
the mode of binding of indole to copper, we believe that a
complex like 7 (Scheme 2), derived from electrophillic metala-
tion of the Cu(4a)2, is likely, as other late metal-indole complexes
where binding occurs via the C3 position of indole have been
reported.15
green solid.13 Gratifyingly, both Cu(I)(4a) and Cu(II)(4a)2
provided the desired product in high yield and enantioselectivity.
While lowering the temperature had no effect on the Cu(I)-
catalyzed reaction, we obtained 3a14 in 91% ee and quantitative
conversion using the Cu(II)(4a)2 catalyst. In contrast, use of
Cu(II)-catalyst 5, which contains a neutral Lewis basic box-
ligand, failed to deliver the desired product (entry 8) in an
appreciable conversion. This observation is consistent with
the decreased electrophilicity of ligated copper species
and demonstrates the potential advantage of X-type chiral
ligands.
With the optimal catalyst and reaction conditions in hand, we
explored the steric and electronic modifications on the substrate
and the nucleophile. Both aromatic and aliphatic alkynes were
suitable substrates for the reaction and could be readily cyclized
to provide the desired furans in high yield and enantioselecti-
vities (Table 2, entries 1ꢀ9). Similarly, electronic variations in
the aryl ring of the indole scaffold were also tolerated, as both
electron donating and withdrawing substituents gave the
desired product in high yields and excellent enantioselectivities
(entries 10ꢀ15). However, 2-methyl indole proved to be a
difficult substrate for the reaction under the standard conditions
as only 16% conversion to the desired product was observed after
48 h at 5 °C.
To explore the mechanism of the Ag(I) and Cu(II) catalyzed
reaction, we monitored the reaction at room temperature by 1H
NMR. When a solution of Ag(4a) (2.5 mol %) was added to a
solution of 1 and 2 in toluene, the reaction begins immediately
and reaches high conversion after a few hours. In contrast, when
a solution of Cu(4a)2 (5 mol %) was added to a solution
containing 1 and 2, the reaction showed a substantial induction
In our initial studies, we observed that 2-methyl indole (6)
reacted very slowly with 1 (Table 2, entry 16). In light of our
mechanistic investigations, we postulated that the decreased
reactivity of 6 might be attributed to the sluggish formation of
the analogous copper-2-methylindole species under catalytic
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Scheme 2. Proposed Mechanism for the Cu(II)-Catalyzed
Reaction of 1 and 2
’ AUTHOR INFORMATION
Corresponding Author
fdtoste@berkeley.edu
’ ACKNOWLEDGMENT
This work has been supported in part by the Director, Office
of Science of the U.S. Department of Energy under Contract No.
DE-AC02-05CH11231. V.R. thanks NSERC for a postdoctoral
fellowship, and Z.J.W. thanks the Hertz Foundation for a graduate
fellowship.
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A proposed mechanism consistent with our findings is shown
in Scheme 2. Copperꢀindole complex 7 is formed when CuX2 is
combined with indole. In the catalytic cycle, this catalyst co-
ordinates to the alkyne, forming intermediate 8, which allows for
addition by the carbonyl to generate a cuprated furan. The chiral
phosphate could control the facial selectivity of the asymmetric
nucleophilic attack on the carbocation through ion pairing in
intermediate 9 or as an anionic ligand through cuprate 10.
Intermolecular nucleophile trapping is followed by protodeme-
talation to regenerate 7.
In conclusion, we have demonstrated the first examples
Ag(I)- and Cu(II)-mediated asymmetric cycloisomerization
reactions triggered by π-activation in which the metal catalysts
is devoid of ancillary L-type ligands.16 The Cu(II)-catalyzed
reaction shows a wide substrate scope and is tolerant to
substitution on the indole and alkyne. Moreover, a copperꢀ
indole complex is proposed to be the active catalyst in the
copper-catalyzed reaction, and incubation of CuX2 and indole
is vital to generating this species. Further work expanding the
utility of these catalysts and concept to other types of metal-
mediated asymmetric transformation is ongoing and will be
reported in due course.
’ ASSOCIATED CONTENT
S
Supporting Information. Complete experimental details
b
including copies of NMR and HPLC traces. This material is
available free of charge via the Internet at http://pubs.acs.org.
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