Competitive formation of spiro[5.5]undecane in preference to bicyclo[4.3.1]decane via type II carbonyl ene reaction

Article abstract of DOI:10.1016/j.tetasy.2005.06.011

The presence of an isopropenyl group at the C-1 position of a 3-isopropenylcyclohexaneacetaldehyde failed to generate the spiro[4.5]decane and produced only bicyclo[4.3.1]decanol. However, the presence of a methallyl group at the C-1 position of 3-isoprop

Full text of DOI:10.1016/j.tetasy.2005.06.011

Tetrahedron:
Asymmetry
Tetrahedron: Asymmetry 16 (2005) 2393–2395
Competitive formation of spiro[5.5]undecane in preference
to bicyclo[4.3.1]decane via type II carbonyl ene reaction
Adusumilli Srikrishna* and Chikkana Dinesh
Department of Organic Chemistry, Indian Institute of Science, Bangalore 560012, India
Received 21 May 2005; accepted 13 June 2005
Abstract—The presence of an isopropenyl group at the C-1 position of a 3-isopropenylcyclohexaneacetaldehyde failed to generate
the spiro[4.5]decane and produced only bicyclo[4.3.1]decanol. However, the presence of a methallyl group at the C-1 position of
3-isopropenylcyclohexaneacetaldehyde generated exclusively the spiro[5.5]undecanols.
ꢀ 2005 Elsevier Ltd. All rights reserved.
1. Introduction
encountered in many natural products.3 In this context,
it was decided to investigate the type II carbonyl ene
reaction of aldehyde 4. Since aldehyde 4 contains
two isopropenyl groups at the C-1 and C-3 positions
of a cyclohexaneacetaldehyde, one would lead to
bi-cyclo[4.3.1]decane and the other to spiro[4.5]decane.
This is an interesting precursor for assessing the utility
of carbonyl ene reactions for the generation of a bridge
system versus a spiro system.
Intramolecular ene reactions in which a carbonyl group
serves as the enophile (commonly referred as carbonyl
ene reactions1) have been widely used in synthesis for
the construction of five-, six- and seven-membered rings.
As in Diels–Alder reactions, Lewis acid catalysis via
complexation with the carbonyl group increases the rate
of the reactions making them useful in natural product
synthesis.1 A cyclohexane ring containing acetaldehyde
and isopropenyl side chains at the 1,3-positions in a
cis orientation was found to be the ideal precursor for
the synthesis of bicyclo[4.3.1]decanes via a carbonyl
ene reaction. The enantioselective syntheses of several
bicyclo[4.3.1]decanes 1 have been accomplished2 in an
efficient manner starting from aldehydes 2, which were
obtained from the readily and abundantly available
monoterpene (R)-carvone 3.
2. Results and discussion
Aldehyde 4 was prepared from (R)-carvone 3 (Scheme
1). An alkylative enone transposition4 was employed
for the generation of 3-isopropenylcarvone 6. Thus,
the regioselective 1,2-addition of isopropenylmagnesium
bromide to carvone 3 in THF followed by oxidation of
the resultant tertiary bi-allylic alcohol 5 with a mixture
of PCC and silica gel in methylene chloride cleanly gen-
erated the transposed dienone 6. Regioselective reduc-
R
O
OH
BF3.Et2O
tion of dienone
6 with LAH in ether at low
temperature (ꢀ70 ꢁC) furnished the syn allyl alcohol 7,
in a highly stereoselective (>97%) manner, in which
the stereochemistry of the allyl alcohol was assigned
on the basis of the well established reduction of 5-substi-
tuted cyclohexenones.5 The ortho-ester Claisen rear-
rangement6 of allyl alcohol 7 with triethyl orthoacetate
and a catalytic amount of propionic acid in a sealed tube
at 180 ꢁC furnished ester 8 in a stereoselective manner.
Reduction of ester 8 with LAH followed by oxidation
of the resultant primary alcohol with PCC and silica
gel in methylene chloride furnished aldehyde 4.
R
CHO
3
2
1
R = H; Me; CH2Ph; CH2CH2Ph;CH2CH2CH=CH2; C≡CPh
The presence of spiro fused systems, either simple or as
part of a polycyclic carbon framework is commonly
*
Corresponding author. Tel.: +91 80 22932215; fax: +91 80
23600683; e-mail: ask@orgchem.iisc.ernet.in
0957-4166/$ - see front matter ꢀ 2005 Elsevier Ltd. All rights reserved.
doi:10.1016/j.tetasy.2005.06.011

2394
A. Srikrishna, C. Dinesh / Tetrahedron: Asymmetry 16 (2005) 2393–2395
O
HO
d
O
OH
O
c
a,b
3
a
b
15
14
e,f
c
3
5
6
7
CHO
CO2Et
HO
e,f
d
CHO
CO2Et
13
16
4
8
Scheme 2. Reagents, conditions and yields: (a) CH2@C(Me)-
CH2MgCl, THF, rt, 8 h; (b) PCC, silica gel, CH2Cl2, rt, 8 h; 65%
(for two steps); (c) LiAlH4, Et2O, ꢀ70 ꢁC, 2 h, 95%; (d) MeC(OEt)3,
EtCO2H, sealed tube, 180 ꢁC, 3 days, 60%; (e) LiAlH4, Et2O, 0 ꢁC, 1 h,
90%; (f) PDC, CH2Cl2, rt, 2 h, 94%.
Scheme 1. Reagents, conditions and yields: (a) CH2@C(Me)MgBr,
THF, rt, 4 h; (b) PCC, silica gel, CH2Cl2, rt, 6 h; 63% (for two steps);
(c) LiAlH4, Et2O, ꢀ70 ꢁC, 2 h, 90%; (d) MeC(OEt)3, EtCO2H, sealed
tube, 180 ꢁC, 4 days, 70%; (e) LiAlH4, Et2O, 0 ꢁC, 0.5 h, 92%; (f) PCC,
silica gel, CH2Cl2, rt, 2 h, 81%.
(Scheme 2). Thus, a 1,2-addition of methallylmagnesium
chloride to carvone 3 in THF at 0 ꢁC followed by oxida-
tion of the resultant alcohol with a mixture of PCC and
silica gel in methylene chloride at room temperature
generated enone 14. Stereo- and regioselective reduction
of enone 14 with LAH followed by an ortho-ester Cla-
isen rearrangement of allyl alcohol 15 with triethyl ortho-
acetate and a catalytic amount of propionic acid in
a sealed tube at 180 ꢁC for 4 days generated ester 16.
Reduction of ester 16 with LAH followed by oxidation
of the primary alcohol with pyridinium dichromate
(PDC) in methylene chloride furnished aldehyde 13.
Treatment of a 0.005 M solution of the aldehyde 13 in
methylene chloride at 0–5 ꢁC with 0.5 equiv of boron tri-
fluoride diethyl etherate for 10 min furnished exclu-
sively7 the spiro[5.5]undecanol 17 (Scheme 3).
Comparison of the spectral data (IR, 1H and 13C
NMR) with that of bicyclo[4.3.1]decanes 1 and 9 con-
firmed that the product formed is the spiro alcohol 17
and not 18. Oxidation of alcohol 17 with PCC and silica
gel in methylene chloride furnished a mixture of ketone
19 and conjugated enone 20, which on treatment with a
catalytic amount of DBU in methylene chloride at room
temperature furnished the conjugated ketone 20.
OH
CHO BF3.Et2O
X
CH2Cl2, 10 min
HO
58%
10
4
9
Treatment of a 0.005 M solution of aldehyde 4 in meth-
ylene chloride with 0.5 equiv of boron trifluoride diethyl
etherate at 5 ꢁC for 10 min unexpectedly furnished only
the endo-bicyclo[4.3.1]decenol 9 in a highly stereoselec-
tive (>95% by NMR) manner with no detectable
amounts of the spiro[4.5]decane 10 being formed. The
structure of alcohol 9 was established from its spectral
data, and further confirmed by the oxidation of alcohol
9 with PCC and sodium acetate in methylene chloride to
furnish ketone 11. Isomerisation of the exomethylene
group in 11 with a catalytic amount of DBU in methyl-
ene chloride furnished the conjugated ketone 12.9
b
a
O
O
HO
9
11
12
(a) PCC, NaOAc, CH2Cl2, rt, 0.5 h, 82%; (b) DBU, CH2Cl2, rt, 3 h, 83%.
Even though it is known that 3-methylenecyclopenta-
To further establish the strategy for the enantioselective
synthesis of spiro[5.5]undecanes, the sequence was also
carried out with dihydrocarvone 21. Thus, partial
hydrogenation of (R)-carvone 3 with Wilkinsonꢀs cata-
lyst8 in benzene at one atmospheric pressure furnished
dihydrocarvone 21, which was transformed into alde-
hyde 22. Treatment of a 0.005 M solution of aldehyde
22 in methylene chloride at 0–5 ꢁC with 0.5 equiv of
boron trifluoride diethyl etherate for 10 min furnished,
as expected, the spiro[5.5]undecanol 23.7 Oxidation of
alcohol 23 with PCC and silica gel in methylene chloride
furnished ketone 24, which on isomerisation with a cat-
nols could be generated from c,d-unsaturated aldehydes
via a Lewis acid catalysis, the reaction is supposed to
proceed via a zwitterion mechanism,1b as the transition
state for the concerted type II ene reaction is very
strained, which explains the failure of the formation of
the spiro system 10 from the aldehyde 4. To substantiate
further, we turned our attention towards the homolo-
gous system 13, which could generate either the bicy-
clo[4.3.1]decane or the spiro[5.5]undecane via the type
II carbonyl ene reaction. Accordingly, the methallyl
group was chosen in place of the isopropenyl group

A. Srikrishna, C. Dinesh / Tetrahedron: Asymmetry 16 (2005) 2393–2395
2395
References
1. (a) Hoffmann, H. M. R. Angew. Chem., Int. Ed. Engl. 1969,
8, 556; (b) Keung, E. C.; Alper, H. J. Chem. Educ. 1972, 49,
97; (c) Snider, B. B.; Rodini, D. J.; Straten, J. V. J. Am.
Chem. Soc. 1980, 102, 5872; (d) Oppolzer, W.; Snieckus, V.
Angew. Chem., Int. Ed. Engl. 1978, 17, 476; (e) Taber, D. F.
Intramolecular Diels–Alder and Alder Ene Reactions;
Springer: Berlin, 1984; (f) Snider, B. B. In Comprehensive
Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Perg-
amon Press: Oxford, 1992; Vol. 5, p 1; (g) Snider, B. B. Acc.
Chem. Res. 1980, 13, 426; (h) Snider, B. B.; Rodini, D. J.;
Karras, M.; Kirk, T. C.; Deutsch, E. A.; Cordova, R.;
Price, R. T. Tetrahedron 1981, 37, 3927.
2. Srikrishna, A.; Dinesh, C.; Anebouselvy, K. Tetrahedron
Lett. 1999, 40, 1031.
3. Sannigrahi, M. Tetrahedron 1999, 55, 9007.
4. Srikrishna, A.; Hemamalini, P. Indian J. Chem. 1990, 29B,
152.
CHO
OH
a
X
HO
18
13
17
b
c
+
O
O
O
19
20
20
Scheme 3. Reagents, conditions and yields: (a) BF3ÆEt2O, CH2Cl2,
5 ꢁC, 10 min, 43%; (b) PCC, silica gel, CH2Cl2, rt, 2 h; (c) DBU,
CH2Cl2, rt, 2 h, 85% (two steps).
5. (a) Wu, Y.-D.; Houk, K. N.; Florez, J.; Trost, B. M. J. Org.
Chem. 1991, 56, 3656; (b) Garver, L.; van Eikeren, P.; Byrd,
J. E. J. Org. Chem. 1976, 41, 2773.
6. Johnson, W. S.; Werthemann, L.; Bartlett, W. R.; Brock-
som, T. J.; Li, T. T.; Faulkner, D. J.; Petersen, M. R. J. Am.
Chem. Soc. 1970, 92, 741.
O
a
b
CHO
3
7. The ene reaction was found to be highly stereoselective
(>95% by 1H and 13C NMR). However, since the next step
is oxidation, no attempt was made to assign the stereo-
chemistry of alcohols 17 and 23.
c
21
22
8. Ireland, R. E.; Bey, P. Org. Synth. 1973, 53, 63.
1
9. All the compounds exhibited the spectral data (IR, H and
13C NMR and mass) consistent with the structures. Yields
refer to isolated and chromatographically pure compounds.
Selected spectral data for the bicyclic enone 12:
O
O
OH
e
d
24
25
24
23
½aꢁD ¼ ꢀ220 (c 0.5, CHCl3). IR (neat): mmax/cmꢀ1 1666,
1
902. H NMR (300 MHz, CDCl3 + CCl4): d 5.87 (1H, s),
Scheme 4. Reagents, conditions and yields: (a) (Ph3P)3RhCl, C6H6,
H2, 1 atm, rt, 2 days, 98%; (b) as in Scheme 2; (c) BF3ÆEt2O, CH2Cl2,
5 ꢁC, 10 min, 60%; (d) PCC, silica gel, CH2Cl2, rt, 2 h; 83%; (e) DBU,
CH2Cl2, rt, 3 h, 92%.
5.44 (1H, d, J = 5.1 Hz), 4.80 (1H, s), 4.75 (1H, s), 2.93 and
2.64 (2H, AB q, J = 15.0 Hz), 2.68 (1H, s), 2.50–2.30 (1H,
m), 2.17 (1H, t of d, J = 13.8 and 3.5 Hz), 2.05–1.90 (2H,
m), 1.96 (3H, s), 1.65 (3H, s), 1.48 (3H, s). 13C NMR
(75 MHz, CDCl3 + CCl4): d 200.0 (C), 155.3 (C), 150.0 (C),
135.8 (C), 130.0 (CH), 121.8 (CH), 111.5 (CH2), 53.0 (CH2),
42.8 (C), 38.7 (CH2), 38.5 (CH), 30.1 (CH2), 27.4 (CH3),
19.1 (CH3), 19.0 (CH3). Mass: m/z 215 (M-1, 5%), 119
(25), 117 (20), 107 (30), 91 (35), 43 (100). For the
alytic amount of DBU in methylene chloride furnished
spirodienone 25 (Scheme 4).
22
spiroenone 20: ½aꢁD ¼ þ44.2 (c 1.2, CHCl3). IR (neat):
m
CDCl3 + CCl4):
max/cmꢀ1 1660, 1645, 885. 1H NMR (300 MHz,
3. Conclusion
d 5.81 (1H, br s), 5.44 (1H, d,
J = 5.2 Hz), 4.62 (1H, s), 4.60 (1H, s), 2.62 (1H, d,
J = 15.6 Hz), 2.49 (1H, d, J = 18.6 Hz), 2.00–1.70 (6H,
m), 1.88 (3H, s), 1.64 (3H, s), 1.62 (3H, s), 1.12 (1H, t,
J = 12.9 Hz). 13C NMR (75 MHz, CDCl3 + CCl4): d 198.9
(C), 158.8 (C), 148.7 (C), 136.9 (C), 125.7 (CH), 125.2 (CH),
109.5 (CH2), 48.4 (CH2), 41.2 (C), 39.3 (CH2), 37.9 (CH),
37.5 (CH2), 31.3 (CH2), 24.7 (CH3), 20.7 (CH3), 19.3 (CH3).
In conclusion, we have demonstrated that the formation
of a spiro[4.5]decanol cannot compete with the forma-
tion of bicyclo[4.3.1]decane via a type II carbonyl ene
reaction of a 1,3-diisopropenylcyclohexaneacetaldehyde.
However, under the same conditions, 1-(2-methylallyl)-
3-isopropenylcyclohexaneacetaldehyde exclusively gen-
erates the spiro[5.5]undecane. Currently, we are investi-
gating the potential of this reaction for the
enantioselective synthesis of natural products containing
a spiro system.
24
For the spiroenone 25: ½aꢁD ¼ þ64.0 (c 0.8, CHCl3). IR
(neat): mmax/cm1 1670. 1H NMR (300 MHz, CDCl3 + CCl4):
d 5.86 (1H, br s), 5.47 (1H, d, J = 4.8 Hz), 2.66 (1H, d,
J = 15.6 Hz), 2.51 and 2.12 (2H, 2 · d, J = 18.6 Hz), 2.10–
1.80 (3H, m), 1.93 (3H, s), 1.75–1.55 (2H, m), 1.62 (3H, s),
1.39 (1H, septet, J = 6.6 Hz), 0.90 (1H, d of t, J = 12.5 and
1.5 Hz), 0.83 (6H, d, J = 6.6 Hz).13C NMR (75 MHz,
CDCl3 + CCl4): d 199.2 (C), 159.0 (C), 137.0 (C), 125.6
(CH), 125.5 (CH), 48.5 (CH2), 41.1 (C), 39.3 (CH2), 36.8
(CH), 36.2 (CH2), 32.2 (CH), 29.5 (CH2), 24.6 (CH3), 20.0
(CH3), 19.5 (CH3), 19.2 (CH3). Mass: m/z 232 (M+,
C16H24O, 30%), 189 (17), 161 (18), 150 (30), 135 (40), 121
(30), 107 (100), 93 (60), 91 (60).
Acknowledgements
We thank the council of scientific and industrial re-
search, New Delhi, for the award of a research fellow-
ship to C.D.