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DOI: 10.1055/s-2003-38357
First Thermal and Transition Metal Catalysed Intramolecular [4+2] Cycloaddition Reactions with N-Tethered Ynamides
Publication History
Publication Date:
28 March 2003 (online)
Abstract
Cationic rhodium(I)-complexes generated from [RhCl(PPh3)3] and AgSbF6 catalyse at room temperature the first examples of intramolecular [4+2] cycloaddition reactions with N-tethered ynamides and provide an efficient access to synthetically versatile tetrahydroindoles.
Key words
ynamides - tetrahydroindoles - Diels-Alder reaction - catalysis - alkynyliodonium salts
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References
Spectral data for dienyne 7: 1H NMR (400 MHz, CDCl3): δ = 7.80 (m, 2 H), 7.35 (m, 2 H), 6.23 (m, 1 H), 6.07 (m, 1 H), 5.55 (m, 1 H), 5.11 (d, J = 16.1 Hz, 1 H), 5.01 (d, J = 9.1 Hz, 1 H), 3.38 (m, 2 H), 2.78 (s, 1 H), 2.43 (s, 3 H), 2.39 (m, 2 H). 13C NMR (100 MHz, CDCl3): δ = 144.7, 136.6, 133.8, 130.0, 129.8, 127.6, 134.6, 116.3, 75.8, 59.5, 50.6, 30.9, 21.6.
11
Experimental Procedure: [RhCl(PPh3)3] (9.3
mg, 0.01 mmol) was added to a solution of ynamide 4-8 (0.20 mmol) in dry toluene (10 mL) under
argon. After stirring for 5 min at r.t., AgSbF6 (0.01
mmol, 0.2 mL of a 0.05 M solution in 1,2-dichloroethane) was added
and the reaction mixture was stirred at r.t. The reaction mixture
was filtered through a small plug of celite, the solvent was evaporated
and the resulting crude product was purified by column chromatography
(Al2O3 III/N, hexanes-EtOAc = 8:2)
to afford 9, 11-14.
Compound 9:
Mp 87-88 °C. 1H NMR
(400 MHz, CDCl3): δ = 7.72
(d, J = 8.4
Hz, 2 H), 7.28 (d, J = 8.4
Hz, 2 H), 5.76 (m, 2 H), 5.66 (m, 1 H), 3.76 (m, 1 H), 3.33 (m,
1 H), 2.77 (m, 2 H), 2.54 (m, 1 H), 2.41 (s, 3 H), 2.02 (m, 1 H),
1.49 (m, 1 H). 13C NMR (100 MHz, CDCl3): δ = 143.6,
137.9, 134.8, 129.5, 127.2, 126.5, 125.3, 103.1, 48.9, 38.0, 28.7,
26.9, 21.5. MS (EI, 70 eV): m/z (%) = 275
(43) [M+], 91 (100). Anal.
Calcd for C15H17NO2S: C, 65.43;
H, 6.22; N, 5.09. Found: C, 65.15; H, 6.06; N, 5.31. Compound 11: Mp 74-75 °C. 1H
NMR (400 MHz, CDCl3): δ = 7.70
(d, J = 8.3
Hz, 2 H), 7.27 (d, J = 8.3
Hz, 2 H), 5.79 (m, 1 H), 5.64 (m, 1 H), 3.46 (m, 2 H), 2.96-2.81
(m, 2 H), 2.47 (s, 3 H), 1.89 (m, 2 H), 1.34 (m, 1 H), 0.35 (s,
9 H). 13C NMR (100 MHz, CDCl3): δ = 145.2,
143.6, 134.8, 129.5, 128.1, 125.9, 125.8, 125.7, 47.2, 36.9, 29.8,
28.7, 21.5, 0.0. MS (EI, 70 eV): m/z (%) = 347
(3) [M+], 99 (100). Anal.
Calcd for C18H25NO2SSi: C, 62.21;
H, 7.25; N, 4.03. Found: C, 61.98; H, 7.35; N, 3.93. Compound 13: Mp 121-122 °C. 1H
NMR (400 MHz, CDCl3): δ = 7.52
(m, 2 H), 7.44 (m, 2 H), 7.32 (m, 2 H), 7.22 (m, 3 H), 5.77 (m,
1 H), 5.70 (m, 1 H), 3.54 (m, 2 H), 3.38 (m, 1 H), 2.78 (m, 1 H),
2.40 (s, 3 H), 2.23 (m, 1 H), 2.11 (m, 1 H), 1.55 (m, 1 H). 13C
NMR (100 MHz, CDCl3): δ = 143.4,
141.0, 134.1, 129.4, 128.0, 127.6, 125.4, 125.3, 124.8, 47.7, 38.0,
33.3, 29.3, 21.6. Compound 14: Oil. 1H
NMR (400 MHz, CDCl3) δ = 7.67
(d, J = 8.2
Hz, 2 H), 7.27 (d, J = 8.2
Hz, 2 H), 5.67 (m, 1 H), 5.54 (m, 1 H), 3.42 (m, 2 H), 2.89 (m,
1 H), 2.60 (m, 2 H), 2.41 (s, 3 H), 2.34 (m, 1 H), 1.87 (m, 2 H),
1.52 (m, 1 H), 1.38 (m, 3 H), 1.28 (m, 1 H), 0.93 (t, J = 7.2 Hz,
3 H). 13C NMR (100 MHz, CDCl3) δ = 143.5,
134.6, 131.8, 129.5, 128.5, 127.8, 125.7, 124.8, 47.9, 36.8, 32.0,
31.0, 29.6, 29.4, 22.9, 21.5, 14.0.
Crystal data for 12:
C13H18NOF3Si, triclinic, space
group
P1 (No. 2), a = 8.896
(2), b = 9.643
(2), c = 9.830
(2) Å, α = 102.38
(3)°, β = 115.97
(3)°, γ = 92.73
(3)°, V = 730.8 (3) Å3, Z = 2, D
c = 1.315
g cm-3, F
(000) = 304,
µ (Mo-Kα) = 1.85
cm-1. 6235 reflections collected, 2650 independent [R(int) = 0.0449],
which were used in all calculations. 172 parameters, R
1 = 0.0457, wR
2 = 0.1129
for observed reflections [F2>2σ(F2)] and R
1 = 0.0597, wR
2 = 0.1217
for all reflections, GoF (on F2) = 0.871.
Max. and min. residual electron densities: 0.285 and -0.231
eÅ-3. Data were collected
on a STOE-IPDS at r.t., the structure was solved by direct methods
using SHELXS-97 and refined using SHELXL-97. CCDC: 194177.