References
1a
Knochel P. In Comprehensive Organic Synthesis
Vol. 4:
Trost B.
Fleming I.
Pergamon Press;
New York:
1991.
p.865
1b
Marek I.
Normant J.-F. In
Cross Coupling Reactions
Diederich D.
Stang P.
VCH;
Weinheim:
1997.
p.271
2
Kitagawa O.
Suzuki T.
Fujiwara H.
Fujita M.
Taguchi T.
Tetrahedron Lett.
1999,
40:
4585
3
Rodriguez AL.
Bunlakananusorn T.
Knochel P.
Org. Lett.
2000,
2:
3285
4 For a review, see: Poli G.
Giambastiani G.
Heumann A.
Tetrahedron
2000,
56:
5959
5a
Kitagawa O.
Suzuki T.
Fujiwara H.
Taguchi T.
Tetrahedron Lett.
1999,
40:
2549
5b
Kitagawa O.
Fujiwara H.
Suzuki T.
Taguchi T.
Shiro M.
J. Org. Chem.
2000,
65:
6819
6a
Rosenblum M.
Rosan A.
Tancrede J.
J. Am. Chem. Soc.
1973,
95:
3062
6b
Lennon P.
Rosan AM.
Rosenblum M.
J. Am. Chem. Soc.
1977,
99:
8426
6c
Rosenblum M.
Acc. Chem. Res.
1974,
122
7
Roberts B.
Wong J.
J. Chem. Soc., Chem. Commun.
1977,
20
8a
Chuang L.-W.
Fu HW.
Sheu BA.
Tau SI.
Yeh M.-C.
J. Am. Chem. Soc.
1993,
115:
5941
8b
Lai M.-L.
Chang S.-C.
Hwu C.-C.
Yeh M.-C.
Tetrahedron Lett.
1996,
37:
6149
8c
Yeh M.-CP.
Chuang L.-W.
Ueng C.-H.
J. Org. Chem.
1996,
61:
3874
9a
Khan MdNI.
Pearson AJ.
J. Am. Chem. Soc.
1984,
106:
1872
9b
Clardy JC.
Cun-heng H.
Khan MdNI.
Pearson AJ.
J. Am. Chem. Soc.
1985,
107:
2748
9c
Khan MdNI.
Pearson AJ.
Tetrahedron Lett.
1985,
26:
1407
10a
Nakamura E.
Kubota K.
Tetrahedron Lett.
1997,
38:
7099
10b
Kubota K.
Nakamura E.
Angew. Chem. Int., Ed. Engl.
1997,
36:
2491
10c
Kubota K.
Nakamura E.
J. Org. Chem.
1997,
62:
792
10d
Nakamura E.
Sakata G.
Kubota K.
Tetrahedron Lett.
1998,
39:
2157
11a
Lorthiois E.
Marek I.
Normant J.-F.
J. Org. Chem.
1998,
63:
566
11b
Lorthiois E.
Marek I.
Normant J.-F.
J. Org. Chem.
1998,
63:
2442
12a
Karoyan P.
Chassaing G.
Tetrahedron Lett.
1997,
38:
85
12b
Karoyan P.
Triolo A.
Nannicini R.
Giannotti D.
Altamura M.
Chassaing G.
Perotta E.
Tetrahedron Lett.
1999,
40:
71
12c
Chassaing G.
Karoyan P.
Tetrahedron: Asymmetry
1997,
8:
2025
12d
Karoyan P.
Chassaing G.
Tetrahedron Lett.
2002,
43:
253
13
Ling R.
Ekhato IV.
Rubin JR.
Wustrow DJ.
Tetrahedron
2001,
57:
6579
14
Compound 3a. Major diastereomer: IR (neat): 3028, 2958, 2872, 2794, 1737, 1495, 1454, 1435, 1366, 1265, 1202, 1170, 1028, 742, 700 cm-1; 1H NMR (400 MHz, CDCl3): δ = 1.16 (3 H, d, J = 6.6 Hz), 2.24 (1 H, dd, J = 9.2, 6.6 Hz), 2.47-2.57 (1 H, m), 2.56-2.62 (1 H, m), 2.78-2.82 (1 H, m), 2.83 (1 H, dd, J = 8.6, 7.6 Hz), 2.89 (1 H, dd, J = 9.7, 6.6 Hz), 3.59 (1 H, d, J = 12.7 Hz), 3.67 (1 H, d, J = 12.7 Hz), 3.70 (3 H, s), 7.25-7.36 (5 H, m); 13C NMR (100 MHz, CDCl3): δ = 19.86, 36.89, 50.60, 51.87, 56.76, 60.20, 61.70, 127.01, 128.31, 128.81, 139.00, 175. 24; Anal. Calcd for C14H19NO2: C, 72.07; H, 8.21; N, 6.00. Found: C, 72.10; H, 8.25; N, 5.98.
15 Crystal structure deposited at the Cambridge Crystallographic Data Centre (deposition numbers 178455).
16 A similar enhanced reactivity of substituted zincated hydrazones compared to unsubstituted ones has been already noticed: see ref.
[10c]
.
17
Compound 3c. IR (neat): 3062, 3027, 2963, 2876, 2792, 1732, 1495, 1453, 1435, 1377, 1263, 1198, 1123, 1072, 1029, 984, 910, 736, 700 cm-1; 1H NMR (500 MHz, CDCl3): δ = 0.99 (3 H, d, J = 7.3 Hz), 1.21 (3 H, s), 2.17-2.22 (1 H, m), 2.30 (1 H, d, J = 9.5 Hz), 2.64-2.71 (1 H, m), 2.91-2.96 (1 H, m), 3.32 (1 H, d, J = 9.5 Hz), 3.57 (1 H, d, J = 13.2 Hz), 3.65 (1 H, J = 13.2 Hz), 3.67 (3 H, s), 7.21-7.37 (5 H, m); 13C NMR (125 MHz, CDCl3): δ = 13.88, 19.27, 38.90, 50.40, 52.03, 60.32, 61.07, 64.68, 126.98, 128.31, 128.68, 139.25, 177.84; Anal. Calcd for C15H21NO2: C, 72.84; H, 8.56; N, 5.66. Found: C, 72.79; H, 8.64; N, 5.74.
18
Compound 3d. IR (neat): 3063, 3027, 2959, 2920, 2791, 1732, 1640, 1495, 1454, 1436, 1377, 1357, 1298, 1216, 1136, 1072, 1028, 992, 914, 735, 699 cm-1; 1H NMR (400 MHz, CDCl3): δ = 1.08 (3 H, d, J = 7.1 Hz), 2.15 (1 H, t, J = 7.1 Hz), 2.23 (1 H, dd, J = 9.5 Hz), 2.35 (1 H, d, J = 9.7 Hz), 2.52-2.63 (2 H, m), 2.95-2.99 (1 H, m), 3.38 (1 H, d, J = 9.9 Hz), 3.60 (1 H, d, J = 13.1 Hz), 3.66 (1 H, d, J = 13.1 Hz), 3.69 (3 H, s), 5.01-5.10 (2 H, m), 5.59-5.69 (1 H, m), 7.22-7.36 (5 H, m); 13C NMR (100 MHz, CDCl3): δ = 14.00, 37.47, 39.89, 51.92, 54.35, 60.22, 61.14, 61.31, 117.85, 126.97, 128.33, 128.64, 134.53, 139.30, 176.61; Anal. Calcd for C17H23NO2: C, 74.69; H, 8.48; N, 5.12. Found: C, 74.68; H, 8.55; N, 5.21.
19
Compound 3e. IR (neat): 3027, 2953, 2932, 2861, 2788, 1732, 1495, 1454, 1378, 1290, 1256, 1196, 1138, 1072, 1029, 738, 699 cm-1; 1H NMR (400 MHz, CDCl3): δ = 0.83 (3 H, t, J = 7.1 Hz), 0.93-1.13 (2 H, m), 0.99 (3 H, d, J = 7.1 Hz), 1.16-1.27 (4 H, m), 1.31-1.39 (1 H, m), 1.62-1.71 (1 H, m), 1.98 (1 H, t, J = 8.6 Hz), 2.08 (1 H, d, J = 9.7 Hz), 2.41-2.51 (1 H, m), 2.91-2.97 (1 H, m), 3.44 (1 H, d, J = 9.7 Hz), 3.51 (1 H, d, J = 13.7 Hz), 3.62 (1 H, d, J = 13.7 Hz), 3.65 (3 H, s), 7.18-7.31 (5 H, m); 13C NMR (100 MHz, CDCl3): δ = 13.91, 14.07, 22.54, 25.28, 32.44, 33.10, 39.80, 51.84, 54.53, 60.28, 61.55, 61.70, 126.87, 128.25, 128.61, 139.31, 177.39; Anal. Calcd for C19H29NO2: C, 75.21; H, 9.63; N, 4.62. Found: C, 75.04; H, 9.64; N, 4.49.
20
Compound 3f. IR (neat): 3062, 3028, 2959, 2795, 1728, 1604, 1495, 1473, 1454, 1436, 1377, 1357, 1314, 1271, 1196, 1133, 1097, 1070, 1029, 910, 735, 701 cm-1; 1H NMR (400 MHz, CDCl3): δ = 1.28 (3 H, d, J = 7.1 Hz), 2.44 (1 H, t, J = 8.6 Hz), 2.60 (1 H, d, J = 9.9 Hz), 2.68 (1 H, m), 2.86 (1 H, d, J = 13.4 Hz), 3.02 (1 H, t, J = 8.6 Hz), 3.24 (1 H, d, J = 9.9 Hz), 3.28 (1 H, d, J = 13.4 Hz), 3.72 (3 H, s), 3.74 (2 H, s), 7.15-7.46 (10 H, m); 13C NMR (100 MHz, CDCl3): δ = 14.06, 38.09, 40.88, 51.78, 55.58, 59.95, 60.27, 60.86, 126.59, 127.05, 128.35, 128.40, 128.82, 129.66, 138.30, 139.13, 176.42; Anal. Calcd for C21H25NO2: C, 77.98; H, 7.79; N, 4.33. Found: C, 78.12; H, 7.73; N, 4.26.
21 Crystal structure deposited at the Cambridge Crystallographic Data Centre (deposition numbers 178454).
22
Compound 5b. IR (neat): 3027, 2950, 2795, 1733, 1494, 1454, 1434, 1374, 1214, 1156, 1112, 1073, 1029, 988, 911, 735, 699 cm-1; 1H NMR (400 MHz, CDCl3): δ = 1.39 (3 H, s), 2.60-2.63 (2 H, m), 3.17-3.30 (3 H, m), 3.41 (1 H, d, J = 9.4 Hz), 3.51-3.52 (1 H, m), 3.74 (1 H, d, J = 13.1 Hz), 3.82 (1 H, d, J = 13.1 Hz), 3.85 (3 H, s), 7.40-7.49 (5 H, m); 13C NMR (100 MHz, CDCl3): δ = 5.22, 18.52, 47.13, 51.14, 52.45, 59.85, 60.66, 65.11, 127.17, 128.42, 128.65, 138.80, 176.61; exact mass (MH+): calcd 374.06, exp. 374.062.
23
Chemla F.
Synlett
1998,
894
24
Compound 5c. IR (neat): 3026, 2949, 2922, 2796, 1731, 1493, 1453, 1434, 1268, 1208, 1158, 1113, 1091, 1028, 1016, 805, 736, 699 cm-1; 1H NMR (400 MHz, CDCl3): δ = 1.30 (3 H, s), 2.32 (3 H, s), 2.40 (1 H, d, J = 9.5 Hz), 2.47 (1 H, t, J = 8.9 Hz), 2.74 (1 H, dd, J = 12.4, 10.9 Hz), 2.85 (1 H, m), 3.04 (1 H, dd, J = 8.9, 7.8 Hz), 3.20 (1 H, d, J = 9.5 Hz), 3.21 (1 H, dd, J = 12.4, 4.5 Hz), 3.58 (1 H, d, J = 13.1 Hz), 3.67 (3 H, s), 3.67 (1 H, d, J = 13.1 Hz), 7.09-7.11 (2 H, d, J = 8.1 Hz), 7.24-7.26 (2 H, d, J = 8.1 Hz), 7.22-7.28 (1 H, m), 7.29-7.31 (4 H, m); 13C NMR (100 MHz, CDCl3): δ = 19.16, 21.05, 34.56, 43.31, 50.37, 52.13, 58.74, 59.97, 64.61, 127.00, 128.28, 128.60, 129.70, 129.75, 132.38, 136.10, 138.74, 176.93; Anal. Calcd for C22H27NO2S: C, 71.51; H, 7.36; N, 3.79. Found: C, 71.41; H, 7.42; N, 3.75.
25
Compound 5d. IR (neat): 3063, 3026, 2975, 2933, 2857, 2791, 1731, 1640, 1495, 1453, 1434, 1373, 1339, 1263, 1209, 1116, 1073, 1028, 992, 911, 740, 699 cm-1; 1H NMR (400 MHz, CDCl3): δ = 1.23 (3 H, s), 1.31-1.40 (1 H, m), 1.60-1.68 (1 H, m), 1.93-2.08 (2 H, m), 2.25 (1 H, t, J = 9.1 Hz), 2.30 (1 H, d, J = 9.3 Hz), 2.55-2.63 (1 H, m), 2.99 (1 H, t, J = 8.3 Hz), 3.28 (1 H, d, J = 9.3 Hz), 3.58 (1 H, d, J = 13.2 Hz), 3.68 (3 H, s), 3.69 (1 H, d, J = 13.2 Hz), 4.94-5.04 (2 H, m), 5.75 (1 H, m), 7.22-7.34 (5 H, m); 13C NMR (100 MHz, CDCl3): δ = 19.27, 28.91, 32.86, 44.08, 50.43, 52.15, 59.30, 60.40, 65.10, 114.82, 127.03, 128.38, 128.68, 138.61, 139.30, 177.83; Anal. Calcd for C18H25NO2: C, 75.22; H, 8.77; N, 4.87. Found: C, 74.93; H, 8.80; N, 4.77.
26 For a review, see: Fürstner A.
Synthesis
1989,
571 ; and references cited therein.
