-
2
-
-
17444401687
-
-
J.-C. Wasilke, S. J. Obrey, R. T. Baker, G. C. Bazan, Chem. Rev. 2005, 105, 1001
-
(2005)
Chem. Rev.
, vol.105
, pp. 1001
-
-
Wasilke, J.-C.1
Obrey, S.J.2
Baker, R.T.3
Bazan, G.C.4
-
3
-
-
84890766709
-
-
Wiley-VCH, Weinheim
-
L. F. Tietze, G. Brasche, K. Gericke, Domino Reactions in Organic Synthesis, Wiley-VCH, Weinheim, 2006
-
(2006)
Domino Reactions in Organic Synthesis
-
-
Tietze, L.F.1
Brasche, G.2
Gericke, K.3
-
4
-
-
33847207721
-
-
K. C. Nicolaou, D. J. Edmonds, P. G. Bulger, Angew. Chem. 2006, 118, 7292
-
(2006)
Angew. Chem.
, vol.118
, pp. 7292
-
-
Nicolaou, K.C.1
Edmonds, D.J.2
Bulger, P.G.3
-
7
-
-
79955410883
-
-
T. Vlaar, E. Ruijter, R. V. A. Orru, Adv. Synth. Catal. 2011, 353, 809
-
(2011)
Adv. Synth. Catal.
, vol.353
, pp. 809
-
-
Vlaar, T.1
Ruijter, E.2
Orru, R.V.A.3
-
8
-
-
84865343822
-
-
L. Lu, J. Chen, W. Xiao, Acc. Chem. Res. 2012, 45, 1278.
-
(2012)
Acc. Chem. Res.
, vol.45
, pp. 1278
-
-
Lu, L.1
Chen, J.2
Xiao, W.3
-
14
-
-
22944485617
-
-
S. Ma, Chem. Rev. 2005, 105, 2829
-
(2005)
Chem. Rev.
, vol.105
, pp. 2829
-
-
Ma, S.1
-
15
-
-
61849124839
-
-
M. Brasholz, H. U. Reissig, R. Zimmer, Acc. Chem. Res. 2009, 42, 45
-
(2009)
Acc. Chem. Res.
, vol.42
, pp. 45
-
-
Brasholz, M.1
Reissig, H.U.2
Zimmer, R.3
-
16
-
-
77952373228
-
-
B. Alcaide, P. Almendros, T. M. d. Campo, Chem. Eur. J. 2010, 16, 5836
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 5836
-
-
Alcaide, B.1
Almendros, P.2
Campo, T.M.D.3
-
17
-
-
79952641846
-
-
C. Aubert, L. Fensterbank, P. Garcia, M. Malacria, A. Simonneau, Chem. Rev. 2011, 111, 1954
-
(2011)
Chem. Rev.
, vol.111
, pp. 1954
-
-
Aubert, C.1
Fensterbank, L.2
Garcia, P.3
Malacria, M.4
Simonneau, A.5
-
23
-
-
22944443077
-
-
in (Ed.: J. Tsuji), Springer, Heidelberg
-
S. Ma, in Topics in Organometallic Chemistry (Ed.:, J. Tsuji,), Springer, Heidelberg, 2005, pp. 183-210.
-
(2005)
Topics in Organometallic Chemistry
, pp. 183-210
-
-
Ma, S.1
-
27
-
-
79951641853
-
-
L. Guo, X. Duan, Y. Liang, Acc. Chem. Res. 2011, 44, 111.
-
(2011)
Acc. Chem. Res.
, vol.44
, pp. 111
-
-
Guo, L.1
Duan, X.2
Liang, Y.3
-
28
-
-
0030600168
-
-
R. Grigg, R. Rasul, J. Redpath, D. Wilson, Tetrahedron Lett. 1996, 37, 4609
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 4609
-
-
Grigg, R.1
Rasul, R.2
Redpath, J.3
Wilson, D.4
-
29
-
-
0030996437
-
-
W. Oppolzer, A. Pimm, B. Stammen, W. E. Hume, Helv. Chim. Acta 1997, 80, 623
-
(1997)
Helv. Chim. Acta
, vol.80
, pp. 623
-
-
Oppolzer, W.1
Pimm, A.2
Stammen, B.3
Hume, W.E.4
-
30
-
-
0031562422
-
-
R. Grigg, R. Rasul, V. Savic, Tetrahedron Lett. 1997, 38, 1825
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 1825
-
-
Grigg, R.1
Rasul, R.2
Savic, V.3
-
33
-
-
8344266012
-
-
F. Wang, X. Tong, J. Cheng, Z. Zhang, Chem. Eur. J. 2004, 10, 5338
-
(2004)
Chem. Eur. J.
, vol.10
, pp. 5338
-
-
Wang, F.1
Tong, X.2
Cheng, J.3
Zhang, Z.4
-
34
-
-
84863376208
-
-
S. Zhao, K. Ji, L. Lu, T. He, A. Zhou, R. Yan, S. Ali, X. Liu, Y. Liang, J. Org. Chem. 2012, 77, 2763.
-
(2012)
J. Org. Chem.
, vol.77
, pp. 2763
-
-
Zhao, S.1
Ji, K.2
Lu, L.3
He, T.4
Zhou, A.5
Yan, R.6
Ali, S.7
Liu, X.8
Liang, Y.9
-
35
-
-
0141806903
-
-
The most commonly observed pathway for the carbopalladation of allenes is the formation of delocalized π-allyl palladium species. See: "Carbopalladation of Allenes": in (Eds.: E. Negishi, A. de Meijere), Wiley-Interscience, New York, p
-
The most commonly observed pathway for the carbopalladation of allenes is the formation of delocalized π-allyl palladium species. See: "Carbopalladation of Allenes":, S. Ma, in Handbook of Organopalladium Chemistry for Organic Synthesis (Eds.:, E. Negishi, A. de Meijere,), Wiley-Interscience, New York, 2002, p. 1491.
-
(2002)
Handbook of Organopalladium Chemistry for Organic Synthesis
, pp. 1491
-
-
Ma, S.1
-
38
-
-
47249124161
-
-
M. D. Lõpez, J. Cobo, M. Nogueras, Curr. Org. Chem. 2008, 12, 718.
-
(2008)
Curr. Org. Chem.
, vol.12
, pp. 718
-
-
Lõpez, M.D.1
Cobo, J.2
Nogueras, M.3
-
40
-
-
69049112844
-
-
Y. Kavanagh, M. O'Brien, P. Evans, Tetrahedron 2009, 65, 8259
-
(2009)
Tetrahedron
, vol.65
, pp. 8259
-
-
Kavanagh, Y.1
O'Brien, M.2
Evans, P.3
-
41
-
-
79952438316
-
-
G. Mehta, R. Samineni, P. Srihari, Tetrahedron Lett. 2011, 52, 1663
-
(2011)
Tetrahedron Lett.
, vol.52
, pp. 1663
-
-
Mehta, G.1
Samineni, R.2
Srihari, P.3
-
43
-
-
84880094219
-
-
E. Elamparuthi, C. Fellay, M. Neuburger, K. Gademann, Angew. Chem. 2012, 124, 4147
-
(2012)
Angew. Chem.
, vol.124
, pp. 4147
-
-
Elamparuthi, E.1
Fellay, C.2
Neuburger, M.3
Gademann, K.4
-
47
-
-
0037176294
-
-
K. M. Brummond, H. Chen, P. Sill, L. You, J. Am. Chem. Soc. 2002, 124, 15186
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 15186
-
-
Brummond, K.M.1
Chen, H.2
Sill, P.3
You, L.4
-
48
-
-
5444224278
-
-
R. Kumareswaran, S. Shin, I. Gallou, T. V. RajanBabu, J. Org. Chem. 2004, 69, 7157
-
(2004)
J. Org. Chem.
, vol.69
, pp. 7157
-
-
Kumareswaran, R.1
Shin, S.2
Gallou, I.3
Rajanbabu, T.V.4
-
49
-
-
24944487677
-
-
M. Murakami, S. Kadowaki, T. Matsuda, Org. Lett. 2005, 7, 3953
-
(2005)
Org. Lett.
, vol.7
, pp. 3953
-
-
Murakami, M.1
Kadowaki, S.2
Matsuda, T.3
-
50
-
-
34250158080
-
-
H. Ohno, T. Mizutani, Y. Kadoh, A. Aso, K. Miyamura, N. Fujii, T, Tanaka, J. Org. Chem. 2007, 72, 4378.
-
(2007)
J. Org. Chem.
, vol.72
, pp. 4378
-
-
Ohno, H.1
Mizutani, T.2
Kadoh, Y.3
Aso, A.4
Miyamura, K.5
Fujii, N.6
Tanaka, T.7
-
51
-
-
33847062476
-
-
S. Ma, Z. Zheng, X. Jiang, Org. Lett. 2007, 9, 529
-
(2007)
Org. Lett.
, vol.9
, pp. 529
-
-
Ma, S.1
Zheng, Z.2
Jiang, X.3
-
52
-
-
53949089396
-
-
X. Jiang, X. Ma, Z. Zheng, S. Ma, Chem. Eur. J. 2008, 14, 8572.
-
(2008)
Chem. Eur. J.
, vol.14
, pp. 8572
-
-
Jiang, X.1
Ma, X.2
Zheng, Z.3
Ma, S.4
-
53
-
-
0001549837
-
-
J. Tsuji, H. Watanabe, I. Minami, I. Shimizu, J. Am. Chem. Soc. 1985, 107, 2196
-
(1985)
J. Am. Chem. Soc.
, vol.107
, pp. 2196
-
-
Tsuji, J.1
Watanabe, H.2
Minami, I.3
Shimizu, I.4
-
56
-
-
84871964283
-
-
Enantioenriched axially chiral allene-propargylic carbonates may be easily prepared from axially chiral α-allenols, which in turn can be accessed according to our recently reported procedure:, J. Ye, W. Fan, S. Ma, Chem. Eur. J. 2013, 19, 716.
-
(2013)
Chem. Eur. J.
, vol.19
, pp. 716
-
-
Ye, J.1
Fan, W.2
Ma, S.3
-
58
-
-
0026722772
-
-
C. G. Frost, J. Howarth, J. M. J. Williams, Tetrahedron: Asymmetry 1992, 3, 1089
-
(1992)
Tetrahedron: Asymmetry
, vol.3
, pp. 1089
-
-
Frost, C.G.1
Howarth, J.2
Williams, J.M.J.3
|