-
2
-
-
0038561146
-
-
(b) Wessjohann, L. A.; Brandt, W.; Thiemann, T. Chem. Rev. 2003, 103, 1625.
-
(2003)
Chem. Rev
, vol.103
, pp. 1625
-
-
Wessjohann, L.A.1
Brandt, W.2
Thiemann, T.3
-
4
-
-
2142690327
-
-
(d) Salaun, J. Chem. Rev. 1989, 89, 1247.
-
(1989)
Chem. Rev
, vol.89
, pp. 1247
-
-
Salaun, J.1
-
5
-
-
0038222536
-
-
(a) Lebel, H.; Marcoux, J.-F.; Molinaro, C.; Charette, A. B. Chem. Rev. 2003, 103, 977.
-
(2003)
Chem. Rev
, vol.103
, pp. 977
-
-
Lebel, H.1
Marcoux, J.-F.2
Molinaro, C.3
Charette, A.B.4
-
9
-
-
84985535088
-
-
(a) Fritschi, H.; Leutenegger, U.; Pfaltz, A. Agnew. Chem., Int. Ed. Engl. 1986, 25, 1005.
-
(1986)
Agnew. Chem., Int. Ed. Engl
, vol.25
, pp. 1005
-
-
Fritschi, H.1
Leutenegger, U.2
Pfaltz, A.3
-
10
-
-
85008090337
-
-
(b) Evans, D. A.; Woerpel, K. A.; Hinman, M. M.; Faul, M. M. J. Am. Chem. Soc. 1991, 113, 726.
-
(1991)
J. Am. Chem. Soc
, vol.113
, pp. 726
-
-
Evans, D.A.1
Woerpel, K.A.2
Hinman, M.M.3
Faul, M.M.4
-
12
-
-
0000795729
-
-
(a) Maxwell, J. L.; O'Malley, S.; Brown, K. C.; Kodadek, T. Organometallics 1992, 11, 645.
-
(1992)
Organometallics
, vol.11
, pp. 645
-
-
Maxwell, J.L.1
O'Malley, S.2
Brown, K.C.3
Kodadek, T.4
-
13
-
-
0000581242
-
-
(b) Doyle, M. P.; Winchester, W. R.; Hoorn, J. A. A.; Lynch, V.; Simonsen, S. H.; Ghosh, R. J. Am. Chem. Soc. 1993, 115, 9968.
-
(1993)
J. Am. Chem. Soc
, vol.115
, pp. 9968
-
-
Doyle, M.P.1
Winchester, W.R.2
Hoorn, J.A.A.3
Lynch, V.4
Simonsen, S.H.5
Ghosh, R.6
-
14
-
-
0029945485
-
-
(c) Davies, H. M. L.; Bruzinski, P. R.; Lake, D. H.; Kong, N.; Fall, M. J. J. Am. Chem. Soc. 1996, 118, 6897.
-
(1996)
J. Am. Chem. Soc
, vol.118
, pp. 6897
-
-
Davies, H.M.L.1
Bruzinski, P.R.2
Lake, D.H.3
Kong, N.4
Fall, M.J.5
-
15
-
-
0000139463
-
-
(a) Nishiyama, H.; Itoh, Y.; Matsumoto, H.; Park, S.-B.; Itoh, K. J. Am. Chem. Soc. 1994, 116, 2223.
-
(1994)
J. Am. Chem. Soc
, vol.116
, pp. 2223
-
-
Nishiyama, H.1
Itoh, Y.2
Matsumoto, H.3
Park, S.-B.4
Itoh, K.5
-
16
-
-
0034794315
-
-
(b) Che, C. M.; Huang, J.-S.; Lee, F.-W.; Li, Y.; Lai, T.-S.; Kwong, H.-L.; Teng, P.-F.; Lee, W.-S.; Lo, W.-C.; Peng, S.-M.; Zhou, Z.-Y. J. Am. Chem. Soc. 2001, 123, 4119.
-
(2001)
J. Am. Chem. Soc
, vol.123
, pp. 4119
-
-
Che, C.M.1
Huang, J.-S.2
Lee, F.-W.3
Li, Y.4
Lai, T.-S.5
Kwong, H.-L.6
Teng, P.-F.7
Lee, W.-S.8
Lo, W.-C.9
Peng, S.-M.10
Zhou, Z.-Y.11
-
17
-
-
0142026526
-
-
(a) Huang, L.; Chen, Y.; Gao, G.-Y.; Zhang, X. P. J. Org. Chem. 2003, 68, 8179.
-
(2003)
J. Org. Chem
, vol.68
, pp. 8179
-
-
Huang, L.1
Chen, Y.2
Gao, G.-Y.3
Zhang, X.P.4
-
18
-
-
8844247934
-
-
(b) Chen, Y.; Fields, K. B.; Zhang, X. P. J. Am. Chem. Soc. 2004, 126, 14718.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 14718
-
-
Chen, Y.1
Fields, K.B.2
Zhang, X.P.3
-
20
-
-
35048898699
-
-
(d) Chen, Y.; Ruppel, J. V.; Zhang, X. P. J. Am. Chem. Soc. 2007, 129, 12074.
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 12074
-
-
Chen, Y.1
Ruppel, J.V.2
Zhang, X.P.3
-
21
-
-
0002746107
-
-
For non-porphyrin Co-catalyzed cyclopropanation systems, see: a
-
For non-porphyrin Co-catalyzed cyclopropanation systems, see: (a) Niimi, T.; Uchida, T.; Irie, R.; Katsuki, T. Adv. Synth. Catal. 2001, 343, 79.
-
(2001)
Adv. Synth. Catal
, vol.343
, pp. 79
-
-
Niimi, T.1
Uchida, T.2
Irie, R.3
Katsuki, T.4
-
22
-
-
0034612061
-
-
(b) Niimi, T.; Uchida, T.; Irie, R.; Katsuki, T. Tetrahedron Lett. 2000, 41, 3647.
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 3647
-
-
Niimi, T.1
Uchida, T.2
Irie, R.3
Katsuki, T.4
-
23
-
-
0035100362
-
-
(c) Ikeno, T.; Nishizuka, A.; Sato, M.; Yamada, T. Synlett 2001, 406.
-
(2001)
Synlett
, pp. 406
-
-
Ikeno, T.1
Nishizuka, A.2
Sato, M.3
Yamada, T.4
-
24
-
-
33947092924
-
-
(d) Nakamura, A.; Konishi, A.; Tatsuno, Y.; Otsuka, S. J. Am. Chem. Soc. 1978, 100, 3443.
-
(1978)
J. Am. Chem. Soc
, vol.100
, pp. 3443
-
-
Nakamura, A.1
Konishi, A.2
Tatsuno, Y.3
Otsuka, S.4
-
25
-
-
0037433496
-
-
(a) Honma, M.; Sawada, T.; Fujisawa, Y.; Utsugi, M.; Watanabe, H.; Umino, A.; Matsumura, T.; Hagihara, T.; Takano, M.; Nakada, M. J. Am. Chem. Soc. 2003, 125, 2860.
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 2860
-
-
Honma, M.1
Sawada, T.2
Fujisawa, Y.3
Utsugi, M.4
Watanabe, H.5
Umino, A.6
Matsumura, T.7
Hagihara, T.8
Takano, M.9
Nakada, M.10
-
28
-
-
37049070734
-
-
For a Rh-based earlier attempt of intramolecular asymmetric cyclopropanation, see
-
For a Rh-based earlier attempt of intramolecular asymmetric cyclopropanation, see: Kennedy, M.; McKervey, M. A.; Maguire, A. R.; Roos, G. H. P. J. Chem. Soc., Chem. Commun. 1990, 361.
-
(1990)
J. Chem. Soc., Chem. Commun
, pp. 361
-
-
Kennedy, M.1
McKervey, M.A.2
Maguire, A.R.3
Roos, G.H.P.4
-
29
-
-
25444440090
-
-
For a Cu-catalyzed asymmetric intermolecular cyclopropanation with α-diazosulfonate esters, see
-
For a Cu-catalyzed asymmetric intermolecular cyclopropanation with α-diazosulfonate esters, see: Ye, T.; Zhou, C. New J. Chem. 2005, 29, 1159.
-
(2005)
New J. Chem
, vol.29
, pp. 1159
-
-
Ye, T.1
Zhou, C.2
-
30
-
-
30944454327
-
-
For a Rh-catalyzed asymmetric cyclopropenation of acetylenes with tosyldiazomethane, see
-
For a Rh-catalyzed asymmetric cyclopropenation of acetylenes with tosyldiazomethane, see: Weatherhead-Kloster, R. A.; Corey, E. J. Org. Lett. 2006, 8, 171.
-
(2006)
Org. Lett
, vol.8
, pp. 171
-
-
Weatherhead-Kloster, R.A.1
Corey, E.J.2
-
31
-
-
12344294527
-
-
For select examples of other approaches for the syntheses and applications of optically active cyclopropyl sulfones, see: (a) Ruano, J. L. G, de Diego, S. A. A, Martin, M. R, Torrente, E, Castro, A. M. M. Org. Lett. 2004, 6, 4945
-
For select examples of other approaches for the syntheses and applications of optically active cyclopropyl sulfones, see: (a) Ruano, J. L. G.; de Diego, S. A. A.; Martin, M. R.; Torrente, E.; Castro, A. M. M. Org. Lett. 2004, 6, 4945.
-
-
-
-
32
-
-
27144499189
-
-
(b) Bernard, A. M.; Frongia, A.; Piras, P. P.; Secci, F.; Spiga, M. Org. Lett. 2005, 7, 4565.
-
(2005)
Org. Lett
, vol.7
, pp. 4565
-
-
Bernard, A.M.1
Frongia, A.2
Piras, P.P.3
Secci, F.4
Spiga, M.5
-
33
-
-
14944347353
-
-
(c) Midura, W. H.; Krysiak, J. A.; Cypryk, M.; Mikolajczyk, M.; Wieczorek, M. W.; Filipczak, A. D. Eur. J. Org. Chem. 2005, 653.
-
(2005)
Eur. J. Org. Chem
, pp. 653
-
-
Midura, W.H.1
Krysiak, J.A.2
Cypryk, M.3
Mikolajczyk, M.4
Wieczorek, M.W.5
Filipczak, A.D.6
-
34
-
-
36649028269
-
-
(d) Das, I.; Pal, T. K.; Pathak, T. J. Org. Chem. 2007, 72, 9181.
-
(2007)
J. Org. Chem
, vol.72
, pp. 9181
-
-
Das, I.1
Pal, T.K.2
Pathak, T.3
-
35
-
-
22244490671
-
-
For an interesting synthesis of cyclopropyl sulfones via Rh-catalyzed intramolecular 1,3 C-H carbene insertion, see: Shi, W.; Zhang, B.; Zhang, J.; Liu, B.; Zhang, S.; Wang, J. Org. Lett. 2005, 7, 3103.
-
For an interesting synthesis of cyclopropyl sulfones via Rh-catalyzed intramolecular 1,3 C-H carbene insertion, see: Shi, W.; Zhang, B.; Zhang, J.; Liu, B.; Zhang, S.; Wang, J. Org. Lett. 2005, 7, 3103.
-
-
-
-
37
-
-
33749081774
-
-
For select examples of chiral ligands with intramolecular hydrogen bonding interactions, see: a
-
For select examples of chiral ligands with intramolecular hydrogen bonding interactions, see: (a) Morice, C.; Le Maux, P.; Simmonneaux, G.; Toupet, L. J. Chem. Soc., Dalton Trans. 1998, 4165.
-
(1998)
J. Chem. Soc., Dalton Trans
, pp. 4165
-
-
Morice, C.1
Le Maux, P.2
Simmonneaux, G.3
Toupet, L.4
-
39
-
-
33750698607
-
-
(c) Liu, Y.; Sandoval, C. A.; Yamaguchi, Y.; Zhang, X.; Wang, Z.; Kato, K.; Ding, K. J. Am. Chem. Soc. 2006, 128, 14212.
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 14212
-
-
Liu, Y.1
Sandoval, C.A.2
Yamaguchi, Y.3
Zhang, X.4
Wang, Z.5
Kato, K.6
Ding, K.7
-
40
-
-
42149141941
-
-
[Co(P6)]-based catalytic system was ineffective for multiple substituted olefins and aliphatic olefins.
-
[Co(P6)]-based catalytic system was ineffective for multiple substituted olefins and aliphatic olefins.
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