-
1
-
-
0003779363
-
-
Beller, M., Bolm, C., Eds.; Wiley-VCH: Weinheim
-
(a) Transition Metals for Organic Synthesis; Beller, M., Bolm, C., Eds.; Wiley-VCH: Weinheim, 1998.
-
(1998)
Transition Metals for Organic Synthesis
-
-
-
4
-
-
0032506945
-
-
For selected recent examples, see: (a) Barnhart, R. W.; Banzan, G. C.; Mourey, T. J. Am. Chem. Soc. 1998, 120, 1082.
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 1082
-
-
Barnhart, R.W.1
Banzan, G.C.2
Mourey, T.3
-
5
-
-
0034684229
-
-
(b) Jeong, N.; Seo, S. D.; Shin, J. Y. J. Am. Chem. Soc. 2000, 122, 10220.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 10220
-
-
Jeong, N.1
Seo, S.D.2
Shin, J.Y.3
-
6
-
-
0002654923
-
-
(c) Lee, P. H.; Sung, S.-y.; Lee, K. Org. Lett. 2001, 3, 3201.
-
(2001)
Org. Lett.
, vol.3
, pp. 3201
-
-
Lee, P.H.1
Sung, S.-Y.2
Lee, K.3
-
7
-
-
0037134803
-
-
(d) Son, S. U.; Park, K. H.; Chung, Y. K. J. Am. Chem. Soc. 2002, 124, 6838.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 6838
-
-
Son, S.U.1
Park, K.H.2
Chung, Y.K.3
-
9
-
-
0034614043
-
-
(b) Lee, M.; Ko, S.; Chang, S. J. Am. Chem. Soc. 2000, 122, 12011.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 12011
-
-
Lee, M.1
Ko, S.2
Chang, S.3
-
11
-
-
0000793297
-
-
(d) Chang, S.; Na, Y.; Choi, E.; Kim, S. Org. Lett. 2001, 3, 2089.
-
(2001)
Org. Lett.
, vol.3
, pp. 2089
-
-
Chang, S.1
Na, Y.2
Choi, E.3
Kim, S.4
-
12
-
-
0035898812
-
-
(e) Chang, S.; Yang, S. H.; Lee, P. H. Tetrahedron Lett. 2001, 42, 4833.
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 4833
-
-
Chang, S.1
Yang, S.H.2
Lee, P.H.3
-
14
-
-
0013379360
-
-
(g) Choi, E.; Lee, C.; Na, Y.; Chang, S. Org. Lett. 2002, 4, 2369.
-
(2002)
Org. Lett.
, vol.4
, pp. 2369
-
-
Choi, E.1
Lee, C.2
Na, Y.3
Chang, S.4
-
15
-
-
0037028575
-
-
Ko, S.; Na, Y.; Chang, S. J. Am. Chem. Soc. 2002, 124, 750.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 750
-
-
Ko, S.1
Na, Y.2
Chang, S.3
-
16
-
-
0001117397
-
-
Although efficiency was generally low (<36% yield), a bimetallic catalytic system of Pd/Ru was previously utilized for the conversion of halobenzenes into aromatic acids with aqueous methyl formate under biphasic conditions at 160 °C, see: Jenner, G.; Taleb, A. B. J. Organomet. Chem. 1994, 470, 257.
-
(1994)
J. Organomet. Chem.
, vol.470
, pp. 257
-
-
Jenner, G.1
Taleb, A.B.2
-
17
-
-
0034614065
-
-
For recent examples of chelation-assisted strategy in metal catalyzed reactions, see: (a) Itami, K.; Mitsudo, K.; Kamei, T.; Koike, T.; Nokami, T.; Yoshida, J. J. Am. Chem. Soc. 2000, 122, 12013. (b) Ishiyama, T.; Hartwig, J. J. Am. Chem. Soc. 2000, 122, 12043. (c) Chatani, N.; Tatamidani, H.; Ie, Y.; Kakiuchi, F.; Murai, S. J. Am. Chem. Soc. 2001, 123, 4849. (d) Jun, C.-H.; Lee, H.; Moon, C. W.; Hong, H.-S. J. Am. Chem. Soc. 2001, 123, 8600.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 12013
-
-
Itami, K.1
Mitsudo, K.2
Kamei, T.3
Koike, T.4
Nokami, T.5
Yoshida, J.6
-
18
-
-
0034614063
-
-
For recent examples of chelation-assisted strategy in metal catalyzed reactions, see: (a) Itami, K.; Mitsudo, K.; Kamei, T.; Koike, T.; Nokami, T.; Yoshida, J. J. Am. Chem. Soc. 2000, 122, 12013. (b) Ishiyama, T.; Hartwig, J. J. Am. Chem. Soc. 2000, 122, 12043. (c) Chatani, N.; Tatamidani, H.; Ie, Y.; Kakiuchi, F.; Murai, S. J. Am. Chem. Soc. 2001, 123, 4849. (d) Jun, C.-H.; Lee, H.; Moon, C. W.; Hong, H.-S. J. Am. Chem. Soc. 2001, 123, 8600.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 12043
-
-
Ishiyama, T.1
Hartwig, J.2
-
19
-
-
0034834214
-
-
For recent examples of chelation-assisted strategy in metal catalyzed reactions, see: (a) Itami, K.; Mitsudo, K.; Kamei, T.; Koike, T.; Nokami, T.; Yoshida, J. J. Am. Chem. Soc. 2000, 122, 12013. (b) Ishiyama, T.; Hartwig, J. J. Am. Chem. Soc. 2000, 122, 12043. (c) Chatani, N.; Tatamidani, H.; Ie, Y.; Kakiuchi, F.; Murai, S. J. Am. Chem. Soc. 2001, 123, 4849. (d) Jun, C.-H.; Lee, H.; Moon, C. W.; Hong, H.-S. J. Am. Chem. Soc. 2001, 123, 8600.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 4849
-
-
Chatani, N.1
Tatamidani, H.2
Ie, Y.3
Kakiuchi, F.4
Murai, S.5
-
20
-
-
0035812386
-
-
For recent examples of chelation-assisted strategy in metal catalyzed reactions, see: (a) Itami, K.; Mitsudo, K.; Kamei, T.; Koike, T.; Nokami, T.; Yoshida, J. J. Am. Chem. Soc. 2000, 122, 12013. (b) Ishiyama, T.; Hartwig, J. J. Am. Chem. Soc. 2000, 122, 12043. (c) Chatani, N.; Tatamidani, H.; Ie, Y.; Kakiuchi, F.; Murai, S. J. Am. Chem. Soc. 2001, 123, 4849. (d) Jun, C.-H.; Lee, H.; Moon, C. W.; Hong, H.-S. J. Am. Chem. Soc. 2001, 123, 8600.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 8600
-
-
Jun, C.-H.1
Lee, H.2
Moon, C.W.3
Hong, H.-S.4
-
21
-
-
0001472631
-
-
12 has been known to catalyze decarbonylation of alkyl formates in the presence of phosphines or N-oxide ligands, see: (a) Kondo, T.; Tantayanon, S.; Tsuji, Y.; Watanabe, Y. Tetrahedron Lett. 1989, 30, 4137. (b) Jenner, G.; Nahmed, E. M.; Leismann, H. J. Organomet. Chem. 1990, 387, 315.
-
(1989)
Tetrahedron Lett.
, vol.30
, pp. 4137
-
-
Kondo, T.1
Tantayanon, S.2
Tsuji, Y.3
Watanabe, Y.4
-
22
-
-
0001041298
-
-
12 has been known to catalyze decarbonylation of alkyl formates in the presence of phosphines or N-oxide ligands, see: (a) Kondo, T.; Tantayanon, S.; Tsuji, Y.; Watanabe, Y. Tetrahedron Lett. 1989, 30, 4137. (b) Jenner, G.; Nahmed, E. M.; Leismann, H. J. Organomet. Chem. 1990, 387, 315.
-
(1990)
J. Organomet. Chem.
, vol.387
, pp. 315
-
-
Jenner, G.1
Nahmed, E.M.2
Leismann, H.3
-
23
-
-
0025776723
-
-
Pd-catalyzed alkoxycarbonylation of aryl halides with alkyl formates in the presence of sodium alkoxides was previously reported, in which sodium alkoxide decarbonylates stoichiometrically formates to provide carbon monoxide, see: Carpentier, J.-F.; Castanet, Y.; Brocard, J.; Mortreux, A.; Petit, F. Tetrahedron Lett. 1991, 32, 4705.
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 4705
-
-
Carpentier, J.-F.1
Castanet, Y.2
Brocard, J.3
Mortreux, A.4
Petit, F.5
-
24
-
-
0035904434
-
-
Recently, it has been revealed that Pd/C is a source of soluble homogeneous catalyst in carbonylation reaction, see: Davies, I. W.; Matty, L.; Hughes, D. L.; Reider, P. J. J. Am. Chem. Soc. 2001, 123, 10139.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 10139
-
-
Davies, I.W.1
Matty, L.2
Hughes, D.L.3
Reider, P.J.4
-
25
-
-
0037162785
-
-
On the basis of this result, a possibility that DMF acts as a CO source through decomposition of DMF could be ruled out, for reference; see: Wan, Y.; Altermann, M.; Larhed, M.; Hallberg, A. J. Org. Chem. 2002, 67, 6232.
-
(2002)
J. Org. Chem.
, vol.67
, pp. 6232
-
-
Wan, Y.1
Altermann, M.2
Larhed, M.3
Hallberg, A.4
-
26
-
-
37049084153
-
-
Buchan, C.; Hamel, N.; Woell, J. B.; Alper, H. J. Chem. Soc., Chem. Commun. 1986, 167.
-
(1986)
J. Chem. Soc., Chem. Commun.
, vol.167
-
-
Buchan, C.1
Hamel, N.2
Woell, J.B.3
Alper, H.4
-
27
-
-
0242414380
-
-
note
-
However, chlorobenzene did not react under the present conditions.
-
-
-
-
28
-
-
0033541041
-
-
Imidoyl triflates were prepared in 70-90% yields starting from the corresponding lactams: Jacobi, P. A.; Liu, H. J. Am. Chem. Soc. 1999, 121, 1958.
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 1958
-
-
Jacobi, P.A.1
Liu, H.2
-
29
-
-
0003445429
-
-
Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer-Verlag: Heidelberg, Chapter 6.2.
-
Blaser, H.-U.; Spindler, F. In Comprehensive Asymmetric Catalysis I; Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer-Verlag: Heidelberg, 1999; Vol. 1, Chapter 6.2.
-
(1999)
Comprehensive Asymmetric Catalysis I
, vol.1
-
-
Blaser, H.-U.1
Spindler, F.2
-
30
-
-
0242666046
-
-
Negishi, E., Ed.; Wiley-Interscience: New York
-
Organopalladium Chemistry for Organic Synthesis; Negishi, E., Ed.; Wiley-Interscience: New York, 2002; Vol. 2, Part VI.
-
(2002)
Organopalladium Chemistry for Organic Synthesis
, vol.2
, Issue.PART VI
-
-
-
31
-
-
0242414379
-
-
note
-
2 (all data) = 0.0754, GOF = 1.180, Z = 11.
-
-
-
-
32
-
-
0032508875
-
-
Fukuyama, T.; Chatani, N.; Tatsumi, J.; Kakiuchi, F.; Murai, S. J. Am. Chem. Soc. 1998, 120, 11522.
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 11522
-
-
Fukuyama, T.1
Chatani, N.2
Tatsumi, J.3
Kakiuchi, F.4
Murai, S.5
-
33
-
-
0000231556
-
-
For a previous report of a crystal structure of a ruthenium cluster with phenanthroline ligand, see: Fish, R. H.; Kim, T.-J.; Stewart, J. L.; Bushweller, J. H.; Rosen, R. K.; Dupon, J. W. Organometallics 1986, 5, 2193.
-
(1986)
Organometallics
, vol.5
, pp. 2193
-
-
Fish, R.H.1
Kim, T.-J.2
Stewart, J.L.3
Bushweller, J.H.4
Rosen, R.K.5
Dupon, J.W.6
-
34
-
-
0037123291
-
-
Recently, the use of aldehyde as a CO source in catalytic Pauson - Khand reaction has been reported, see: (a) Morimoto, T.; Fuji, K.; Tsutsumi, K.; Kakiuchi, K. J. Am. Chem. Soc. 2002, 124, 3806. (b) Shibata, T.; Toshida, N.; Takagi, K. Org. Lett. 2002, 4, 1619.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 3806
-
-
Morimoto, T.1
Fuji, K.2
Tsutsumi, K.3
Kakiuchi, K.4
-
35
-
-
0000348065
-
-
Recently, the use of aldehyde as a CO source in catalytic Pauson - Khand reaction has been reported, see: (a) Morimoto, T.; Fuji, K.; Tsutsumi, K.; Kakiuchi, K. J. Am. Chem. Soc. 2002, 124, 3806. (b) Shibata, T.; Toshida, N.; Takagi, K. Org. Lett. 2002, 4, 1619.
-
(2002)
Org. Lett.
, vol.4
, pp. 1619
-
-
Shibata, T.1
Toshida, N.2
Takagi, K.3
|