-
1
-
-
79953006738
-
-
For reviews, see
-
For reviews, see
-
-
-
-
11
-
-
77954100129
-
-
R. Wakabayashi, D. Fujino, S. Hayashi, H. Yorimitsu, K. Oshima, J. Org. Chem. 2010, 75, 4337
-
(2010)
J. Org. Chem.
, vol.75
, pp. 4337
-
-
Wakabayashi, R.1
Fujino, D.2
Hayashi, S.3
Yorimitsu, H.4
Oshima, K.5
-
13
-
-
62549103403
-
-
M. Iwasaki, H. Yorimitsu, K. Oshima, Bull. Chem. Soc. Jpn. 2009, 82, 249
-
(2009)
Bull. Chem. Soc. Jpn.
, vol.82
, pp. 249
-
-
Iwasaki, M.1
Yorimitsu, H.2
Oshima, K.3
-
14
-
-
58149204024
-
-
Y. Sumida, S. Hayashi, K. Hirano, H. Yorimitsu, K. Oshima, Org. Lett. 2008, 10, 1629
-
(2008)
Org. Lett.
, vol.10
, pp. 1629
-
-
Sumida, Y.1
Hayashi, S.2
Hirano, K.3
Yorimitsu, H.4
Oshima, K.5
-
15
-
-
40649116007
-
-
Y. Sumida, Y. Takada, S. Hayashi, K. Hirano, H. Yorimitsu, K. Oshima, Chem. Asian J. 2008, 3, 119
-
(2008)
Chem. Asian J.
, vol.3
, pp. 119
-
-
Sumida, Y.1
Takada, Y.2
Hayashi, S.3
Hirano, K.4
Yorimitsu, H.5
Oshima, K.6
-
16
-
-
35548964277
-
-
S. Hayashi, K. Hirano, H. Yorimitsu, K. Oshima, J. Am. Chem. Soc. 2007, 129, 12650
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 12650
-
-
Hayashi, S.1
Hirano, K.2
Yorimitsu, H.3
Oshima, K.4
-
17
-
-
34247121057
-
-
M. Iwasaki, S. Hayashi, K. Hirano, H. Yorimitsu, K. Oshima, J. Am. Chem. Soc. 2007, 129, 4463
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 4463
-
-
Iwasaki, M.1
Hayashi, S.2
Hirano, K.3
Yorimitsu, H.4
Oshima, K.5
-
18
-
-
34247896944
-
-
M. Jang, S. Hayashi, K. Hirano, H. Yorimitsu, K. Oshima, Tetrahedron Lett. 2007, 48, 4003
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 4003
-
-
Jang, M.1
Hayashi, S.2
Hirano, K.3
Yorimitsu, H.4
Oshima, K.5
-
19
-
-
34247872786
-
-
M. Iwasaki, S. Hayashi, K. Hirano, H. Yorimitsu, K. Oshima, Tetrahedron 2007, 63, 5200
-
(2007)
Tetrahedron
, vol.63
, pp. 5200
-
-
Iwasaki, M.1
Hayashi, S.2
Hirano, K.3
Yorimitsu, H.4
Oshima, K.5
-
20
-
-
33745535959
-
-
Y. Takada, S. Hayashi, K. Hirano, H. Yorimitsu, K. Oshima, Org. Lett. 2006, 8, 2515
-
(2006)
Org. Lett.
, vol.8
, pp. 2515
-
-
Takada, Y.1
Hayashi, S.2
Hirano, K.3
Yorimitsu, H.4
Oshima, K.5
-
21
-
-
33644519289
-
-
S. Hayashi, K. Hirano, H. Yorimitsu, K. Oshima, J. Am. Chem. Soc. 2006, 128, 2210.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 2210
-
-
Hayashi, S.1
Hirano, K.2
Yorimitsu, H.3
Oshima, K.4
-
24
-
-
4143056958
-
-
D. Nečas, M. Turský, M. Kotora, J. Am. Chem. Soc. 2004, 126, 10222
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 10222
-
-
Nečas, D.1
Turský, M.2
Kotora, M.3
-
25
-
-
67649855290
-
-
H. Miura, K. Wada, S. Hosokawa, M. Sai, T. Kondo, M. Inoue, Chem. Commun. 2009, 4112
-
(2009)
Chem. Commun.
, pp. 4112
-
-
Miura, H.1
Wada, K.2
Hosokawa, S.3
Sai, M.4
Kondo, T.5
Inoue, M.6
-
26
-
-
18244427166
-
-
T. Kondo, K. Kodoi, E. Nishinaga, T. Okada, Y. Morisaki, Y. Watanabe, T. Mitsudo, J. Am. Chem. Soc. 1998, 120, 5587
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 5587
-
-
Kondo, T.1
Kodoi, K.2
Nishinaga, E.3
Okada, T.4
Morisaki, Y.5
Watanabe, Y.6
Mitsudo, T.7
-
27
-
-
45549087381
-
-
R. Shintani, K. Takatsu, T. Hayashi, Org. Lett. 2008, 10, 1191.
-
(2008)
Org. Lett.
, vol.10
, pp. 1191
-
-
Shintani, R.1
Takatsu, K.2
Hayashi, T.3
-
28
-
-
33748278352
-
-
For an example of tin-catalyzed retro-allylation of tertiary homoallyl alcohols, see
-
For an example of tin-catalyzed retro-allylation of tertiary homoallyl alcohols, see:, A. Yanagisawa, T. Aoki, T. Arai, Synlett 2006, 2071.
-
(2006)
Synlett
, pp. 2071
-
-
Yanagisawa, A.1
Aoki, T.2
Arai, T.3
-
29
-
-
79952998053
-
-
For reviews about copper catalysis in carbon-carbon and carbon-heteroatom bond formation, see
-
For reviews about copper catalysis in carbon-carbon and carbon-heteroatom bond formation, see
-
-
-
-
34
-
-
51049095122
-
-
G. Evano, N. Blanchard, M. Toumi, Chem. Rev. 2008, 108, 3054.
-
(2008)
Chem. Rev.
, vol.108
, pp. 3054
-
-
Evano, G.1
Blanchard, N.2
Toumi, M.3
-
35
-
-
77952794676
-
-
S. Chiba, L. Zhang, J.-Y. Lee, J. Am. Chem. Soc. 2010, 132, 7266
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 7266
-
-
Chiba, S.1
Zhang, L.2
Lee, J.-Y.3
-
36
-
-
77951056826
-
-
T. Sugiishi, A. Kimura, H. Nakamura, J. Am. Chem. Soc. 2010, 132, 5332
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 5332
-
-
Sugiishi, T.1
Kimura, A.2
Nakamura, H.3
-
37
-
-
77953624675
-
-
C. He, S. Guo, L. Huang, A. Lei, J. Am. Chem. Soc. 2010, 132, 8273
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 8273
-
-
He, C.1
Guo, S.2
Huang, L.3
Lei, A.4
-
38
-
-
67749108291
-
-
I. Nakamura, T. Araki, M. Terada, J. Am. Chem. Soc. 2009, 131, 2804
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 2804
-
-
Nakamura, I.1
Araki, T.2
Terada, M.3
-
39
-
-
27644503604
-
-
M. Tokunaga, Y. Shirogane, H. Aoyama, Y. Obora, Y. Tsuji, J. Organomet. Chem. 2005, 690, 5378.
-
(2005)
J. Organomet. Chem.
, vol.690
, pp. 5378
-
-
Tokunaga, M.1
Shirogane, Y.2
Aoyama, H.3
Obora, Y.4
Tsuji, Y.5
-
40
-
-
79953000580
-
-
Addition of stoichiometric amounts of allylmetals to carbonyl compounds is known to be a reversible process involving C-C bond cleavage. Mg
-
Addition of stoichiometric amounts of allylmetals to carbonyl compounds is known to be a reversible process involving C-C bond cleavage. Mg
-
-
-
-
41
-
-
0001690531
-
-
Li
-
R. A. Bensker, M. P. Siklosi, E. C. Mozdzen, J. Am. Chem. Soc. 1978, 100, 2134; Li
-
(1978)
J. Am. Chem. Soc.
, vol.100
, pp. 2134
-
-
Bensker, R.A.1
Siklosi, M.P.2
Mozdzen, E.C.3
-
44
-
-
2442473025
-
-
Zn
-
K. Fujita, H. Yorimitsu, K. Oshima, Chem. Rec. 2004, 4, 110; Zn
-
(2004)
Chem. Rec.
, vol.4
, pp. 110
-
-
Fujita, K.1
Yorimitsu, H.2
Oshima, K.3
-
48
-
-
57549095572
-
-
For selected examples of NHC-Cu complexes and their use in catalysis, see J. R. Herron, Z. T. Ball, J. Am. Chem. Soc. 2008, 130, 16486
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 16486
-
-
Herron, J.R.1
Ball, Z.T.2
-
49
-
-
58149385034
-
-
T. Ohishi, M. Nishiura, Z. Hou, Angew. Chem. 2008, 120, 5876
-
(2008)
Angew. Chem.
, vol.120
, pp. 5876
-
-
Ohishi, T.1
Nishiura, M.2
Hou, Z.3
-
51
-
-
33748047505
-
-
D. S. Laitar, E. Y. Tsui, J. P. Sadighi, J. Am. Chem. Soc. 2006, 128, 11036
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 11036
-
-
Laitar, D.S.1
Tsui, E.Y.2
Sadighi, J.P.3
-
52
-
-
29044433052
-
-
D. S. Laitar, P. Müller, J. P. Sadighi, J. Am. Chem. Soc. 2005, 127, 17196
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 17196
-
-
Laitar, D.S.1
Müller, P.2
Sadighi, J.P.3
-
53
-
-
0141631426
-
-
V. Jurkauskas, J. P. Sadighi, S. L. Buchwald, Org. Lett. 2003, 5, 2417
-
(2003)
Org. Lett.
, vol.5
, pp. 2417
-
-
Jurkauskas, V.1
Sadighi, J.P.2
Buchwald, S.L.3
-
54
-
-
33846081585
-
-
H. Lebel, M. Davi, S. Diez-Gonzalez, S. P. Nolan, J. Org. Chem. 2007, 72, 144
-
(2007)
J. Org. Chem.
, vol.72
, pp. 144
-
-
Lebel, H.1
Davi, M.2
Diez-Gonzalez, S.3
Nolan, S.P.4
-
55
-
-
77951933689
-
-
C. A. Citadelle, E. Le-Nouy, F. Bisaro, A. M. Z. Slawin, C. S. J. Cazin, Dalton Trans. 2010, 39, 4489
-
(2010)
Dalton Trans.
, vol.39
, pp. 4489
-
-
Citadelle, C.A.1
Le-Nouy, E.2
Bisaro, F.3
Slawin, A.M.Z.4
Cazin, C.S.J.5
-
56
-
-
78650911789
-
-
I. I. F. Boogaerts, G. C. Fortman, M. R. L. Furst, C. S. J. Cazin, S. P. Nolan, Angew. Chem. 2010, 122, 8856
-
(2010)
Angew. Chem.
, vol.122
, pp. 8856
-
-
Boogaerts, I.I.F.1
Fortman, G.C.2
Furst, M.R.L.3
Cazin, C.S.J.4
Nolan, S.P.5
-
58
-
-
79953019676
-
-
T. Fujihara, T. Xu, K. Semba, J. Terao, Y. Tsuji, Angew. Chem. 2011, 123, 543
-
(2011)
Angew. Chem.
, vol.123
, pp. 543
-
-
Fujihara, T.1
Xu, T.2
Semba, K.3
Terao, J.4
Tsuji, Y.5
-
60
-
-
1542647135
-
-
H. Kaur, F. K. Zinn, E. D. Stevens, S. P. Nolan, Organometallics 2004, 23, 1157
-
(2004)
Organometallics
, vol.23
, pp. 1157
-
-
Kaur, H.1
Zinn, F.K.2
Stevens, E.D.3
Nolan, S.P.4
-
63
-
-
34247102222
-
-
S. A. Delp, C. Munro-Leighton, L. A. Goj, M. A. Ramirez, T. B. Gunnoe, J. J. L. Petersen, P. D. Boyle, Inorg. Chem. 2007, 46, 2365.
-
(2007)
Inorg. Chem.
, vol.46
, pp. 2365
-
-
Delp, S.A.1
Munro-Leighton, C.2
Goj, L.A.3
Ramirez, M.A.4
Gunnoe, T.B.5
Petersen, J.J.L.6
Boyle, P.D.7
-
64
-
-
84908659806
-
-
Other NHC ligands such as SIPr, IMes, SIMes were used in a similar capacity. Phosphine ligands were completely useless. For a review on N-heterocyclic carbenes in late-transition-metal catalysis, see
-
Other NHC ligands such as SIPr, IMes, SIMes were used in a similar capacity. Phosphine ligands were completely useless. For a review on N-heterocyclic carbenes in late-transition-metal catalysis, see:, S. Díez-González, N. Marion, S. P. Nolan, Chem. Rev. 2009, 109, 3612.
-
(2009)
Chem. Rev.
, vol.109
, pp. 3612
-
-
Díez-González, S.1
Marion, N.2
Nolan, S.P.3
-
65
-
-
2442615966
-
-
For stoichiometric zirconium-mediated allyl transfer reaction by retro-allylation of secondary homoallyl alcohols, see
-
For stoichiometric zirconium-mediated allyl transfer reaction by retro-allylation of secondary homoallyl alcohols, see:, K. Fujita, H. Yorimitsu, H. Shinokubo, K. Oshima, J. Org. Chem. 2004, 69, 3302.
-
(2004)
J. Org. Chem.
, vol.69
, pp. 3302
-
-
Fujita, K.1
Yorimitsu, H.2
Shinokubo, H.3
Oshima, K.4
-
66
-
-
0003417469
-
-
(Eds.: B.-M. Trost, I. Fleming), Pergamon, Oxford
-
H. Yamamoto, in Comprehensive Organic Synthesis (Eds.:, B.-M. Trost, I. Fleming,), Pergamon, Oxford, 1991
-
(1991)
Comprehensive Organic Synthesis
-
-
Yamamoto, H.1
-
67
-
-
0003627206
-
-
(Ed.: S. Patai), Wiley, New York
-
J. L. Moreau, in The Chemistry of Ketenes, Allenes, and Related Compounds, Part-1 (Ed.:, S. Patai,), Wiley, New York, 1980
-
(1980)
The Chemistry of Ketenes, Allenes, and Related Compounds, Part-1
-
-
Moreau, J.L.1
-
68
-
-
0004226727
-
-
(Eds.: E. Buncel, T. Durst), Wiley, New York
-
R. Epsztein, in Comprehensive Carbanion Chemistry (Eds.:, E. Buncel, T. Durst,), Wiley, New York, 1980.
-
(1980)
Comprehensive Carbanion Chemistry
-
-
Epsztein, R.1
-
69
-
-
0028962259
-
-
For examples of metal-promoted selective allenylation or propargylation of carbonyl compounds, see T. Nakagawa, A. Kasatkin, F. Sato, Tetrahedron Lett. 1995, 36, 3207
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 3207
-
-
Nakagawa, T.1
Kasatkin, A.2
Sato, F.3
-
70
-
-
0000986355
-
-
K. Furuta, M. Ishiguro, R. Haruta, N. Ikeda, H. Yamamoto, Bull. Chem. Soc. Jpn. 1984, 57, 2768
-
(1984)
Bull. Chem. Soc. Jpn.
, vol.57
, pp. 2768
-
-
Furuta, K.1
Ishiguro, M.2
Haruta, R.3
Ikeda, N.4
Yamamoto, H.5
-
71
-
-
38149116921
-
-
B. Alcaide, P. Almendros, M. C. Redondo, Chem. Eur. J. 2008, 14, 637
-
(2008)
Chem. Eur. J.
, vol.14
, pp. 637
-
-
Alcaide, B.1
Almendros, P.2
Redondo, M.C.3
-
72
-
-
34547214986
-
-
B. Alcaide, P. Almendros, T. Martínez-del-Campo, Angew. Chem. 2006, 118, 4613
-
(2006)
Angew. Chem.
, vol.118
, pp. 4613
-
-
Alcaide, B.1
Almendros, P.2
Martínez-Del-Campo, T.3
-
74
-
-
11844305031
-
-
B. Alcaide, P. Almendros, C. Aragoncillo, M. C. Redondo, Eur. J. Org. Chem. 2005, 98
-
(2005)
Eur. J. Org. Chem.
, pp. 98
-
-
Alcaide, B.1
Almendros, P.2
Aragoncillo, C.3
Redondo, M.C.4
-
75
-
-
0037006835
-
-
B. Alcaide, P. Almendros, C. Aragoncillo, Chem. Eur. J. 2002, 8, 1719
-
(2002)
Chem. Eur. J.
, vol.8
, pp. 1719
-
-
Alcaide, B.1
Almendros, P.2
Aragoncillo, C.3
-
76
-
-
66149186743
-
-
D. Seomoon, J. A, P. H. Lee, Org. Lett. 2009, 11, 2401
-
(2009)
Org. Lett.
, vol.11
, pp. 2401
-
-
Seomoon, D.1
A, J.2
Lee, P.H.3
-
79
-
-
0035851247
-
-
V. Nair, C. N. Jayan, S. Ros, Tetrahedron 2001, 57, 9453
-
(2001)
Tetrahedron
, vol.57
, pp. 9453
-
-
Nair, V.1
Jayan, C.N.2
Ros, S.3
-
80
-
-
0032538497
-
-
X.-H. Yi, Y. Meng, X.-G. Hua, C.-J. Li, J. Org. Chem. 1998, 63, 7472
-
(1998)
J. Org. Chem.
, vol.63
, pp. 7472
-
-
Yi, X.-H.1
Meng, Y.2
Hua, X.-G.3
Li, C.-J.4
-
86
-
-
79953004215
-
-
The structure of 9aa was unambiguously identified by spectroscopic and X-ray crystallographic analysis. See the Supporting Information for details. CCDC-800252 (9aa) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
-
The structure of 9aa was unambiguously identified by spectroscopic and X-ray crystallographic analysis. See the Supporting Information for details. CCDC-800252 (9aa) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.
-
-
-
-
87
-
-
79953015662
-
-
Au
-
Au 99, 991.
-
-
-
-
89
-
-
51049085597
-
-
Pd
-
M. Álvarez-Corral, M. Muñoz-Dorado, I. Rodríguez- García, Chem. Rev. 2008, 108, 3174; Pd
-
(2008)
Chem. Rev.
, vol.108
, pp. 3174
-
-
Álvarez-Corral, M.1
Muñoz-Dorado, M.2
Rodríguez- García, I.3
-
90
-
-
0038373078
-
-
S. Ma, F. Yu, W. Gao, J. Org. Chem. 2003, 68, 5943
-
(2003)
J. Org. Chem.
, vol.68
, pp. 5943
-
-
Ma, S.1
Yu, F.2
Gao, W.3
-
92
-
-
0035844713
-
-
W. F. J. Karstens, D. Klomp, F. P. J. T. Rutjes, H. Hiemstra, Tetrahedron 2001, 57, 5123
-
(2001)
Tetrahedron
, vol.57
, pp. 5123
-
-
Karstens, W.F.J.1
Klomp, D.2
Rutjes, F.P.J.T.3
Hiemstra, H.4
-
93
-
-
0033617429
-
-
H. Ohno, A. Toda, Y. Miwa, T. Taga, E. Osawa, Y. Yamaoka, N. Fujii, T. Ibuka, J. Org. Chem. 1999, 64, 2992
-
(1999)
J. Org. Chem.
, vol.64
, pp. 2992
-
-
Ohno, H.1
Toda, A.2
Miwa, Y.3
Taga, T.4
Osawa, E.5
Yamaoka, Y.6
Fujii, N.7
Ibuka, T.8
-
95
-
-
79953011312
-
-
Cyclization of aminoallenes
-
Cyclization of aminoallenes
-
-
-
-
96
-
-
33747139387
-
-
ring-closing metathesis
-
F. Bellina, R. Rossi, Tetrahedron 2006, 62, 7213; ring-closing metathesis
-
(2006)
Tetrahedron
, vol.62
, pp. 7213
-
-
Bellina, F.1
Rossi, R.2
-
98
-
-
37549061707
-
-
F. Boeda, H. Clavier, M. Jordaan, W. H. Meyer, S. P. Nolan, J. Org. Chem. 2008, 73, 259
-
(2008)
J. Org. Chem.
, vol.73
, pp. 259
-
-
Boeda, F.1
Clavier, H.2
Jordaan, M.3
Meyer, W.H.4
Nolan, S.P.5
-
99
-
-
33645458762
-
-
cyclization of 4-chloro-2-butenylamines
-
R. Castarlenas, C. Vovard, C. Fischmeister, P. H. Dixneuf, J. Am. Chem. Soc. 2006, 128, 4079; cyclization of 4-chloro-2-butenylamines
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 4079
-
-
Castarlenas, R.1
Vovard, C.2
Fischmeister, C.3
Dixneuf, P.H.4
-
101
-
-
0035909620
-
-
cycloaddition
-
M. P. Green, J. C. Prodger, A. E. Sherlock, C. J. Hayes, Org. Lett. 2001, 3, 3377; cycloaddition
-
(2001)
Org. Lett.
, vol.3
, pp. 3377
-
-
Green, M.P.1
Prodger, J.C.2
Sherlock, A.E.3
Hayes, C.J.4
-
102
-
-
55249089671
-
-
biological properties
-
L.-G. Meng, P. Cai, Q. Guo, S. Xue, J. Org. Chem. 2008, 73, 8491; biological properties
-
(2008)
J. Org. Chem.
, vol.73
, pp. 8491
-
-
Meng, L.-G.1
Cai, P.2
Guo, Q.3
Xue, S.4
-
103
-
-
46149136196
-
-
T. A. Smith, S. J. Croker, R. S. T. Loeffler, Phytochemistry 1986, 25, 683
-
(1986)
Phytochemistry
, vol.25
, pp. 683
-
-
Smith, T.A.1
Croker, S.J.2
Loeffler, R.S.T.3
-
105
-
-
42149150961
-
-
S. Hayashi, K. Hirano, H. Yorimitsu, K. Oshima, J. Am. Chem. Soc. 2008, 130, 5048.
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 5048
-
-
Hayashi, S.1
Hirano, K.2
Yorimitsu, H.3
Oshima, K.4
-
110
-
-
0032514971
-
-
P. Moya, Á. Cantín, M.-A. Castillo, J. Primo, M. A. Miranda, E. Primo-Yúfera, J. Org. Chem. 1998, 63, 8530.
-
(1998)
J. Org. Chem.
, vol.63
, pp. 8530
-
-
Moya, P.1
Cantín, Á.2
Castillo, M.-A.3
Primo, J.4
Miranda, M.A.5
Primo-Yúfera, E.6
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