References and Notes
For selected reviews, see:
<A NAME="RU09306ST-1A">1a</A>
Trost BM.
Krische MJ.
Synlett
1998,
1
<A NAME="RU09306ST-1B">1b</A>
Aubert C.
Buisine O.
Malacria M.
Chem. Rev.
2002,
102:
813
<A NAME="RU09306ST-1C">1c</A>
Echavarren AM.
Nevado C.
Chem. Soc. Rev.
2004,
33:
431
<A NAME="RU09306ST-2A">2a</A> For reviews of Au-catalyzed reactions, see:
Dyker G.
Angew. Chem. Int. Ed.
2000,
39:
4237
<A NAME="RU09306ST-2B">2b</A>
Hashmi ASK.
Gold Bull.
2003,
36:
3
<A NAME="RU09306ST-2C">2c</A> For selected examples for gold carbene species, see:
Luzung MR.
Markham JP.
Toste FD.
J. Am. Chem. Soc.
2004,
126:
10858
<A NAME="RU09306ST-2D">2d</A>
Zhang L.
Kozmin SA.
J. Am. Chem. Soc.
2004,
126:
11806
<A NAME="RU09306ST-2E">2e</A>
Zhang L.
Kozmin SA.
J. Am. Chem. Soc.
2005,
127:
6963
<A NAME="RU09306ST-2F">2f</A>
Nieto-Oberhuber C.
López S.
Echavarren AM.
J. Am. Chem. Soc.
2005,
127:
6178
<A NAME="RU09306ST-2G">2g</A>
Fürstner A.
Hannen P.
Chem. Commun.
2004,
2546
<A NAME="RU09306ST-3A">3a</A>
Shin S.
Gupta AK.
Rhim CY.
Oh CH.
Chem. Commun.
2005,
4429
<A NAME="RU09306ST-3B">3b</A> For recent benzannulation of enynals, see:
Kim N.
Kim YM.
Park W.
Sung D.
Gupta AK.
Oh CH.
Org. Lett.
2005,
7:
5289
<A NAME="RU09306ST-3C">3c</A>
Ohe K.
Miki K.
Yokoi T.
Nishino F.
Uemura S.
Organometallics
2000,
19:
5525
<A NAME="RU09306ST-3D">3d</A>
Ohe K.
Yokoi T.
Miki K.
Nishino F.
Uemura S.
J. Am. Chem. Soc.
2002,
124:
526
<A NAME="RU09306ST-4A">4a</A>
Myers AG.
Harrington PM.
Kown BM.
J. Am. Chem. Soc.
1992,
114:
1086
<A NAME="RU09306ST-4B">4b</A>
Sugiyama H.
Fujiwara T.
Kawabata H.
Yoda N.
Hirayama N.
Saito I.
J. Am. Chem. Soc.
1992,
114:
5573
<A NAME="RU09306ST-5">5</A>
Zhao J.
Hughes CO.
Toste FD.
J. Am. Chem. Soc.
2006,
128:
7436
<A NAME="RU09306ST-6">6</A>
Georgy M.
Boucard V.
Campagne J.-M.
J. Am. Chem. Soc.
2005,
127:
14180
<A NAME="RU09306ST-7">7</A>
General experimental procedure (3a): To a mixture of PPh3 (2.6 mg, 0.01 mmol) and NaAuCl4·H2O (3.6 mg, 0.01 mmol) in dry DCE (0.2 mL) under an argon atmosphere at 0 °C was added
a solution of yne-propargylic acetate 1a (100 mg, 0.30 mmol) in DCE (1.0 mL). The resulting reaction mixture was stirred at
r.t. for 0.5 → 4 h. Upon completion of the reaction, monitored by TLC, the reaction
mixture was concentrated in vacuo and the residue was subjected to flash column chromatography
(hexane-EtOAc, 20:1) to afford the corresponding product 3a (72.4 mg, 83%); FT-IR (NaCl): 3058, 2961, 2926, 2864, 2362, 2335, 1686, 1627, 1588,
1491, 1452 cm-1; 1H NMR (400 MHz, CDCl3): δ = 8.00 (s, 1 H), 7.93 (d, J = 8.05 Hz, 1 H), 7.88 (d, J = 8.00 Hz, 1 H), 7.85 (s, 1 H), 7.61-7.51 (m, 2 H), 7.48-7.38 (m, 5 H), 2.35 (t, J = 7.4 Hz, 2 H), 1.44 (quint, J = 7.4 Hz, 2 H), 1.18-1.06 (m, 2 H), 0.74 (t, J = 7.4 Hz, 3 H); 13C NMR (100 MHz, CDCl3): δ = 207.88, 141.09, 139.85, 137.45, 134.15, 132.07, 129.49, 129.15, 129.03, 129.89,
128.82, 128.20, 128.04, 127.99, 127.86, 126.96, 42.88, 26,93, 22.36, 13.90; HRMS:
m/z calcd for C21H20ONa+: 311.1411; found: 311.1402. 3b: FT-IR (NaCl): 2958, 2929, 2864, 1682, 1635, 1593, 1461 cm-1; 1H NMR (400 MHz, CDCl3): δ = 8.48 (s, 1 H), 8.11-7.82 (m, 4 H), 7.58 (dddd, J = 18.31, 8.15, 6.86, 1.37 Hz, 2 H), 3.11 (t, J = 7.4 Hz, 2 H), 1.87-1.70 (m, 2 H), 1.52-1.41 (m, 2 H), 0.99 (t, J = 7.4 Hz, 2 H); 13C NMR (100 MHz, CDCl3): δ = 200.55, 135.47, 134.39, 132.52, 129.71, 129.66, 129.58, 129.55, 129.50, 128.45,
128.35, 128.29, 127.79, 127.73, 126.67, 124.00, 123.94, 38.40, 26.63, 22.52, 13.97;
HRMS: m/z calcd for C15H16ONa+: 235.1099; found: 235.1102. 3e: FT-IR (NaCl): 3051, 2991, 2957, 2927, 2870, 1687, 1626, 1581, 1506, 1454, 1390 cm-1; 1H NMR (400 MHz, CDCl3): δ = 8.19 (s, 1 H), 8.08-7.82 (m, 5 H), 7.73-7.34 (m, 7 H), 2.31-2.10 (m, 2 H),
1.30-1.13 (m, 2 H), 0.98-0.80 (m, 2 H), 0.58 (t, J = 7.3 Hz, 3 H); 13C NMR (100 MHz, CDCl3): δ = 206.20, 140.32, 139.01, 135.76, 134.19, 133.83, 132.39, 132.32, 130.97, 129.04,
128.60, 128.57, 128.39, 128.22, 128.02, 127.73, 127.11, 126.69, 126.26, 126.06, 125.54,
41.96, 26.69, 22.20, 13.78; HRMS: m/z calcd for C25H22ONa+: 361.1568; found: 361.1577. 3f: FT-IR (NaCl): 3056, 2965, 2905, 2865, 1686, 1597, 1485, 1477, 1451, 1362, 1274 cm-1; 1H NMR (400 MHz, CDCl3): δ = 7.88 (ddd, J = 9.37, 7.48, 3.72 Hz, 3 H), 7.62 (s, 1 H), 7.57-7.51 (m, 2 H), 7.50-7.45 (m, 2 H),
7.45-7.33 (m, 3 H), 0.93 (s, 9 H); 13C NMR (100 MHz, CDCl3): δ = 216.76, 141.18, 140.04, 136.40, 133.32, 131.75, 130.11, 130.02, 128.95, 128.83,
128.73, 128.12, 127.82, 127.19, 126.89, 125.17, 45.26, 27.57; HRMS: m/z calcd for C21H20ONa+: 311.1412; found: 311.1417. 3h: FT-IR (NaCl): 3059, 1651, 1624, 1597, 1465, 1442, 1380, 1349, 1283, 1233 cm-1; 1H NMR (400 MHz, CDCl3): δ = 8.28 (s, 1 H), 7.99-7.90 (m, 4 H), 7.89-7.85 (m, 2 H), 7.67-7.60 (m, 2 H),
7.59-7.50 (m, 5 H); 13C NMR (100 MHz, CDCl3): δ = 196.97, 138.13, 135.49, 135.05, 132.60, 132.48, 132.09, 130.32, 129.64, 128.71,
128.68, 128.65, 128.56, 128.54, 128.52, 128.04, 127.02, 126.01, 94.70; HRMS: m/z calcd for C17H12ONa+: 255.0786; found: 255.0781. 3i: FT-IR (NaCl): 2958, 2928, 2865, 1962, 1754, 1666, 1562, 1466, 1367, 1277, 1205 cm-1; 1H NMR (400 MHz, CDCl3): δ = 8.04 (s, 1 H), 7.98-7.90 (m, 3 H), 7.75-7.68 (m, 2 H), 7.66-7.53 (m, 2 H),
7.49-7.41 (m, 1 H), 7.39-7.28 (m, 5 H), 7.25-7.16 (m, 3 H); 13C NMR (100 MHz, CDCl3): δ = 198.57, 198.53, 140.56, 138.74, 137.93, 137.61, 134.29, 133.06, 131.78, 130.26,
129.67, 129.57, 129.43, 129.31, 128.65, 128.52, 128.35, 128.18, 128.05, 127.44, 127.04;
HRMS: m/z calcd for C23H16ONa+: 331.1099; found: 331.1110. 3j: FT-IR (NaCl): 3054, 2927, 2861, 2364, 2333, 1662, 1596, 1446, 1280, 1222 cm-1; 1H NMR (400 MHz, CDCl3): δ = 8.18 (s, 1 H), 8.00 (d, J = 10.46 Hz, 2 H), 7.94 (d, J = 7.94 Hz, 1 H), 7.78 (t, J = 8.65, 8.65 Hz, 2 H), 7.72-7.59 (m, 3 H), 7.55-7.50 (m, 2 H), 7.45-7.32 (m, 4 H),
7.32-7.25 (m, 2 H), 7.12 (t, J = 7.82 Hz, 2 H); 13C NMR (100 MHz, CDCl3): δ = 198.11, 138.63, 138.19, 137.86, 136.87, 134.11, 133.58, 132.51, 132.19, 131.98,
130.96, 129.78, 129.69, 128.85, 128.33, 128.29, 128.20, 128.15, 128.11, 128.04, 127.91,
127.17, 126.28, 126.24, 125.87, 125.12; HRMS: m/z calcd for C27H18ONa+: 381.1255; found: 381.1263. 7e: FT-IR (NaCl): 3050, 2961, 2934, 2866, 2242, 1937, 1811, 1594, 1489, 1451, 1387,
1315 cm-1; 1H NMR (400 MHz, CDCl3): δ = 8.04 (s, 1 H), 7.98-7.90 (m, 3 H), 7.75-7.68 (m, 2 H), 7.66-7.53 (m, 2 H),
7.49-7.41 (m, 1 H), 7.39-7.28 (m, 5 H), 7.25-7.16 (m, 3 H), 3.10 (m, 2 H), 2.22 (td,
J = 12.4, 4.4 Hz, 1 H), 2.08 (dt, J = 12.4, 4.4 Hz, 1 H), 1.23-1.15 (m, 4 H), 0.92 (m, 3 H), 0.51 (t, J = 7.4 Hz, 3 H); 13C NMR (100 MHz, CDCl3): δ = 198.57, 198.53, 140.56, 138.74, 137.93, 137.61, 134.29, 133.06, 131.78, 130.26,
129.67, 129.57, 129.43, 129.31, 128.65, 128.52, 128.35, 128.18, 128.05, 127.44, 127.04;
HRMS:
m/z calcd for C27H26ONa+: 389.1881; found: 389.1890.
For Au- or Ag-catalyzed [3,3]-sigmatropic rearrangement of propargylic acetates, see:
<A NAME="RU09306ST-8A">8a</A>
Zhang L.
Wang S.
J. Am. Chem. Soc.
2006,
128:
1442
<A NAME="RU09306ST-8B">8b</A>
Zhang L.
J. Am. Chem. Soc.
2005,
127:
16804
<A NAME="RU09306ST-8C">8c</A>
Buzas A.
Istrate F.
Gagosz F.
Org. Lett.
2006,
8:
1957
<A NAME="RU09306ST-8D">8d</A>
Sromek AW.
Kelin AV.
Gevorgyan V.
Angew. Chem. Int. Ed.
2004,
43:
2280
<A NAME="RU09306ST-9A">9a</A>
Asao N.
Takahashi K.
Lee S.
Kasahara T.
Yamamoto Y.
J. Am. Chem. Soc.
2002,
124:
12650
<A NAME="RU09306ST-9B">9b</A>
Yao T.
Zhang X.
Larock RC.
J. Am. Chem. Soc.
2004,
126:
11164
<A NAME="RU09306ST-10">10</A>
Shah BK.
Neckers DC.
Chem. Mater.
2006,
18:
603
