-
1
-
-
1642409515
-
-
For reviews on transition-metal catalyzed carbon-heteroatom bond formations, see: (a) Prim, D.; Andrioletti, B.; Rose-Munch, F.; Rose, E.; Couty, F. Tetrahedron 2004, 60, 3325.
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Prim, D.1
Andrioletti, B.2
Rose-Munch, F.3
Rose, E.4
Couty, F.5
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3
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0037060980
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-
(c) Prim, D.; Campagne, J.-M.; Joseph, D.; Andrioletti, B. Tetrahedron 2002, 58, 2041.
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Prim, D.1
Campagne, J.-M.2
Joseph, D.3
Andrioletti, B.4
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6
-
-
0001038733
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-
(f) Wolfe, J. P.; Wagaw, S.; Marcoux, J.-F.; Buchwald, S. L. Acc. Chem. Res. 1998, 31, 805.
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Wolfe, J.P.1
Wagaw, S.2
Marcoux, J.-F.3
Buchwald, S.L.4
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9
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0032125820
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-
(a) He, F.; Foxman, B. M.; Snider, B. B. J. Am. Chem. Soc. 1998, 120, 6417.
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J. Am. Chem. Soc.
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He, F.1
Foxman, B.M.2
Snider, B.B.3
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10
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-
0032079256
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-
(b) Morita, S.; Kitano, K.; Matsubara, J.; Ohtani, T.; Kawano, Y.; Otsubo, K.; Uchida, M. Tetrahedron 1998, 54, 4811.
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Morita, S.1
Kitano, K.2
Matsubara, J.3
Ohtani, T.4
Kawano, Y.5
Otsubo, K.6
Uchida, M.7
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11
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-
9644304518
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-
(a) Beccalli, E. M.; Broggini, G.; Paladino, G.; Zoni, C. Tetrahedron 2005, 61, 61.
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Beccalli, E.M.1
Broggini, G.2
Paladino, G.3
Zoni, C.4
-
12
-
-
0037163272
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-
(b) Ferreira, I. C. F. R.; Queiroz, M.-J. R. P.; Kirsch, G. Tetrahedron 2002, 58, 7943.
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Ferreira, I.C.F.R.1
Queiroz, M.-J.R.P.2
Kirsch, G.3
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13
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-
2942615843
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-
(c) López-Rodríguez, M. L.; Benhamú, B.; Ayala, D.; Rominguera, J. L.; Murcia, M.; Ramos, J. A.; Viso, A. Tetrahedron 2000, 56, 3245.
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López-Rodríguez, M.L.1
Benhamú, B.2
Ayala, D.3
Rominguera, J.L.4
Murcia, M.5
Ramos, J.A.6
Viso, A.7
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14
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0034712156
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-
(a) Wolfe, J. P.; Tomori, H.; Sadighi, J. P.; Yin, J.; Buchwald, S. L. J. Org. Chem. 2000, 65, 1158.
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-
Wolfe, J.P.1
Tomori, H.2
Sadighi, J.P.3
Yin, J.4
Buchwald, S.L.5
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15
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-
0032560932
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-
(b) Old, D. W.; Wolfe, J. P.; Buchwald, S. L. J. Am. Chem. Soc. 1998, 120, 9722.
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Old, D.W.1
Wolfe, J.P.2
Buchwald, S.L.3
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18
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-
1242351224
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-
Yoshikawa, S.; Odaira, J.; Kitamura, Y.; Bedekar, A. V.; Furuta, T.; Tanaka, K. Tetrahedron 2004, 60, 2225.
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-
Yoshikawa, S.1
Odaira, J.2
Kitamura, Y.3
Bedekar, A.V.4
Furuta, T.5
Tanaka, K.6
-
19
-
-
0034006866
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-
Our group has used the structurally related optically active 8,8′-disubstituted 1,1′-binaphthyls as chiral modifiers. For examples, see: (a) Fuji, K.; Ohnishi, H.; Moriyama, S.; Tanaka, K.; Kawabata, T.; Tsubaki, K. Synlett 2000, 351.
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(2000)
Synlett
, pp. 351
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-
Fuji, K.1
Ohnishi, H.2
Moriyama, S.3
Tanaka, K.4
Kawabata, T.5
Tsubaki, K.6
-
20
-
-
0032791097
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-
(b) Tanaka, K.; Nuruzzaman, M.; Yoshida, M.; Asakawa, N.; Yang, X.-S.; Tsubaki, K.; Fuji, K. Chem. Pharm. Bull. 1999, 47, 1053.
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Chem. Pharm. Bull.
, vol.47
, pp. 1053
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-
Tanaka, K.1
Nuruzzaman, M.2
Yoshida, M.3
Asakawa, N.4
Yang, X.-S.5
Tsubaki, K.6
Fuji, K.7
-
21
-
-
0033551929
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-
(c) Fuji, K.; Yang, X.-S.; Ohnishi, H.; Hao, X.-J.; Obata, Y.; Tanaka, K. Tetrahedron: Asymmetry 1999, 10, 3243.
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Tetrahedron: Asymmetry
, vol.10
, pp. 3243
-
-
Fuji, K.1
Yang, X.-S.2
Ohnishi, H.3
Hao, X.-J.4
Obata, Y.5
Tanaka, K.6
-
22
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-
0031566725
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-
(d) Tanaka, K.; Asakawa, N.; Nuruzzaman, M.; Fuji, K. Tetrahedron: Asymmetry 1997, 8, 3637.
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(1997)
Tetrahedron: Asymmetry
, vol.8
, pp. 3637
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-
Tanaka, K.1
Asakawa, N.2
Nuruzzaman, M.3
Fuji, K.4
-
23
-
-
30544454131
-
-
note
-
+, 419.1564; found, 419.1531.
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-
-
-
24
-
-
0346786657
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-
For reviews on the Suzuki-Miyaura cross-coupling, see: (a) Suzuki, A. J. Organomet. Chem. 1999, 576, 147.
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(1999)
J. Organomet. Chem.
, vol.576
, pp. 147
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-
Suzuki, A.1
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26
-
-
30544445309
-
-
note
-
+, 419.1564; found, 419.1524.
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-
-
-
28
-
-
0029874188
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-
(b) Wolfe, J. P.; Rennels, R. A.; Buchwald, S. L. Tetrahedron 1996, 52, 7525.
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(1996)
Tetrahedron
, vol.52
, pp. 7525
-
-
Wolfe, J.P.1
Rennels, R.A.2
Buchwald, S.L.3
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29
-
-
30544444296
-
-
note
-
2; hexane-EtOAc, 3:2) to afford 13 (88 mg, 85%).
-
-
-
-
30
-
-
30544447383
-
-
note
-
3 (1.4 equiv) in toluene at 100 °C for 36 h to give 13 in 82%; see, ref. 12a.
-
-
-
-
32
-
-
0035904989
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-
(b) Baillie, C.; Chen, W.; Xiao, J. Tetrahedron Lett. 2001, 42, 9085.
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(2001)
Tetrahedron Lett.
, vol.42
, pp. 9085
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-
Baillie, C.1
Chen, W.2
Xiao, J.3
-
33
-
-
30544444693
-
-
note
-
The starting material 12 was recovered in 72% yield. No reductive dehalogenation of 12 as a side reaction was observed.
-
-
-
-
34
-
-
0038788901
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1- coordination, see: Reid, S. M.; Boyle, R. C.; Mague, J. T.; Fink, M. J. J. Am. Chem. Soc. 2003, 125, 7816.
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(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 7816
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-
Reid, S.M.1
Boyle, R.C.2
Mague, J.T.3
Fink, M.J.4
-
35
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0037138687
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2-coordination, see: Yin, J.; Rainka, M. P.; Zhang, X.-X.; Buchwald, S. L. J. Am. Chem. Soc. 2002, 124, 1162.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 1162
-
-
Yin, J.1
Rainka, M.P.2
Zhang, X.-X.3
Buchwald, S.L.4
-
36
-
-
30544441775
-
-
note
-
Attempts to synthesize the eight-, nine-, and ten-membered lactams using 23, 24, and 25 as the starting materials, respectively, were unsuccessful (Figure 2). In every case only the starting materials were recovered. (Diagram presented). Figure 2. Substrates for eight- to ten-membered lactam information.
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