-
1
-
-
0001796781
-
-
For recent reviews, see
-
For recent reviews, see: Reissig, H.-U. Top. Curr. Chem. 1988, 144, 73-135
-
(1988)
Top. Curr. Chem.
, vol.144
, pp. 73-135
-
-
Reissig, H.-U.1
-
8
-
-
33749858163
-
-
Carson, C. A.; Kerr, M. A. Angew. Chem., Int. Ed. 2006, 45, 6560-6563
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 6560-6563
-
-
Carson, C.A.1
Kerr, M.A.2
-
10
-
-
34548204750
-
-
Kalidindi, S.; Jeong, W. B.; Schall, A.; Bandichhor, R.; Nosse, B.; Reiser, O. Angew. Chem., Int. Ed. 2007, 46, 6361-6363
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 6361-6363
-
-
Kalidindi, S.1
Jeong, W.B.2
Schall, A.3
Bandichhor, R.4
Nosse, B.5
Reiser, O.6
-
11
-
-
54749144499
-
-
Leduc, A. B.; Kerr, M. A. Angew. Chem., Int. Ed. 2008, 47, 7945-7948
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 7945-7948
-
-
Leduc, A.B.1
Kerr, M.A.2
-
13
-
-
46949091089
-
-
Pohlhaus, P. D.; Sanders, S. D.; Parsons, A. T.; Li, W.; Johnson, J. S. J. Am. Chem. Soc. 2008, 130, 8642-8650
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 8642-8650
-
-
Pohlhaus, P.D.1
Sanders, S.D.2
Parsons, A.T.3
Li, W.4
Johnson, J.S.5
-
17
-
-
76249087704
-
-
Karadeolian, A.; Kerr, M. A. Angew. Chem., Int. Ed. 2010, 49, 1133-1135
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 1133-1135
-
-
Karadeolian, A.1
Kerr, M.A.2
-
19
-
-
18244384582
-
-
In;, Eds.; John Wiley & Sons Ltd.: Chichester, England,; Part I
-
Wiberg, K. B. In The Chemistry of Cyclobutanes; Rappoport, Z.; Liebman, J. F., Eds.; John Wiley & Sons Ltd.: Chichester, England, 2005; Part I, pp 4 - 5.
-
(2005)
The Chemistry of Cyclobutanes
, pp. 4-5
-
-
Wiberg, K.B.1
Rappoport, Z.2
Liebman, J.F.3
-
20
-
-
0011562591
-
-
Shimada, S.; Saigo, K.; Nakamura, H.; Hasegawa, M. Chem. Lett. 1991, 20, 1149-1152
-
(1991)
Chem. Lett.
, vol.20
, pp. 1149-1152
-
-
Shimada, S.1
Saigo, K.2
Nakamura, H.3
Hasegawa, M.4
-
21
-
-
0030702056
-
-
Yokozawa, T.; Tagami, M.; Takehana, T.; Suzuki, T. Tetrahedron 1997, 53, 15603-15616
-
(1997)
Tetrahedron
, vol.53
, pp. 15603-15616
-
-
Yokozawa, T.1
Tagami, M.2
Takehana, T.3
Suzuki, T.4
-
22
-
-
51349131363
-
-
Matsuo, J.-I.; Sasaki, S.; Tanaka, H.; Ishibashi, H. J. Am. Chem. Soc. 2008, 130, 11600-11601
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 11600-11601
-
-
Matsuo, J.-I.1
Sasaki, S.2
Tanaka, H.3
Ishibashi, H.4
-
23
-
-
69449094221
-
-
Matsuo, J.-I.; Sasaki, S.; Hoshikawa, T.; Ishibashi, H. Org. Lett. 2009, 11, 3822-3825
-
(2009)
Org. Lett.
, vol.11
, pp. 3822-3825
-
-
Matsuo, J.-I.1
Sasaki, S.2
Hoshikawa, T.3
Ishibashi, H.4
-
25
-
-
72649103798
-
-
Allart, E. A.; Christie, S. D. R.; Pritchard, G. J.; Elsegood, M. R. Chem. Commun. 2009, 47, 7339-7341
-
(2009)
Chem. Commun.
, vol.47
, pp. 7339-7341
-
-
Allart, E.A.1
Christie, S.D.R.2
Pritchard, G.J.3
Elsegood, M.R.4
-
26
-
-
69249239139
-
-
Matsuo, J.-I.; Negishi, S.; Ishibashi, H. Tetrahedron Lett. 2009, 50, 5831-5833
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 5831-5833
-
-
Matsuo, J.-I.1
Negishi, S.2
Ishibashi, H.3
-
27
-
-
77954556406
-
-
Matsuo, J.-I.; Okado, R.; Ishibashi, H. Org. Lett. 2010, 12, 3266-3268
-
(2010)
Org. Lett.
, vol.12
, pp. 3266-3268
-
-
Matsuo, J.-I.1
Okado, R.2
Ishibashi, H.3
-
29
-
-
78049499860
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3 has been a successful catalyst for both cyclopropane and cyclobutane cycloadditions; see refs 1d, 2c, 2d, 2f, 2i, and 5
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3 has been a successful catalyst for both cyclopropane and cyclobutane cycloadditions; see refs 1d, 2c, 2d, 2f, 2i, and 5
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Jackson, S. K.; Karadeolian, A.; Driega, A. B.; Kerr, M. A. J. Am. Chem. Soc. 2008, 130, 4196-4201
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 4196-4201
-
-
Jackson, S.K.1
Karadeolian, A.2
Driega, A.B.3
Kerr, M.A.4
-
32
-
-
55049131715
-
-
Ivanova, O. A.; Budynina, E. M.; Grishin, Y. K.; Trushkov, I. V.; Verteletshii, P. V. Eur. J. Org. Chem. 2008, 5329-5335
-
(2008)
Eur. J. Org. Chem.
, pp. 5329-5335
-
-
Ivanova, O.A.1
Budynina, E.M.2
Grishin, Y.K.3
Trushkov, I.V.4
Verteletshii, P.V.5
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78049526004
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See Supporting Information
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See Supporting Information.
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Reactions with this cyclobutane were conducted at -50 °C; see Supporting Information
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Reactions with this cyclobutane were conducted at -50 °C; see Supporting Information.
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