-
1
-
-
33845435469
-
-
For recent reviews of transition metal-catalyzed higher-order carbocyclization reactions, see
-
For recent reviews of transition metal-catalyzed higher-order carbocyclization reactions, see: Aubert, C.; Fensterbank, L.; Gandon, V.; Malacria, M. Top. Organomet. Chem. 2006, 19, 259
-
(2006)
Top. Organomet. Chem.
, vol.19
, pp. 259
-
-
Aubert, C.1
Fensterbank, L.2
Gandon, V.3
Malacria, M.4
-
3
-
-
3342979429
-
-
For recent examples of DFT calculations on the understanding of rhodium-catalyzed [ m + n ] and [ m + n + o ] carbocyclization reactions, see the following. [(5+2)]
-
For recent examples of DFT calculations on the understanding of rhodium-catalyzed [ m + n ] and [ m + n + o ] carbocyclization reactions, see the following. [(5+2)]: Yu, Z.-X.; Wender, P. A.; Houk, K. N. J. Am. Chem. Soc. 2004, 126, 9154
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 9154
-
-
Yu, Z.-X.1
Wender, P.A.2
Houk, K.N.3
-
4
-
-
13644255984
-
-
[4+(2+2)]
-
[4+(2+2)]: Baik, M.-H.; Baum, E. W.; Burland, M. C.; Evans, P. A. J. Am. Chem. Soc. 2005, 127, 1602
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 1602
-
-
Baik, M.-H.1
Baum, E.W.2
Burland, M.C.3
Evans, P.A.4
-
5
-
-
42649096946
-
-
[(2+2)+1]
-
[(2+2)+1]: Pitcock, W. H., Jr.; Lord, R. L.; Baik, M.-H. J. Am. Chem. Soc. 2008, 130, 5821
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 5821
-
-
Pitcock Jr., W.H.1
Lord, R.L.2
Baik, M.-H.3
-
6
-
-
42449109584
-
-
[2+2+2+1]
-
[2+2+2+1]: Montero-Campillo, M. M.; Rodríguez-Otero, J.; Cabaleiro-Lago, E. J. Phys. Chem. A 2008, 112, 2423
-
(2008)
J. Phys. Chem. A
, vol.112
, pp. 2423
-
-
Montero-Campillo, M.M.1
Rodríguez-Otero, J.2
Cabaleiro-Lago, E.3
-
7
-
-
34548185894
-
-
[5+2+1]
-
[5+2+1]: Wang, Y.; Wang, J.; Su, J; Huang, F.; Jiao, L; Liang, Y; Yang, D.; Zhang, S.; Wender, P. A.; Yu, Z. J. Am. Chem. Soc. 2007, 129, 10060-10061
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 10060-10061
-
-
Wang, Y.1
Wang, J.2
Su, J.3
Huang, F.4
Jiao, L.5
Liang, Y.6
Yang, D.7
Zhang, S.8
Wender, P.A.9
Yu, Z.10
-
8
-
-
84890780346
-
-
For recent reviews of PK reactions, see: In;, Ed.; Wiley-VCH: Weinheim, Ch. 11, pp.
-
For recent reviews of PK reactions, see: Jeong, N. In Modern Rhodium-Catalyzed Organic Reactions; Evans, P. A., Ed.; Wiley-VCH: Weinheim, 2005, Ch. 11, pp 215.
-
(2005)
Modern Rhodium-Catalyzed Organic Reactions
, pp. 215
-
-
Jeong, N.1
Evans, P.A.2
-
12
-
-
0032360438
-
-
2, see
-
2, see: Koga, Y.; Kobayashi, T.; Narasaka, K. Chem. Lett. 1998, 249
-
(1998)
Chem. Lett.
, pp. 249
-
-
Koga, Y.1
Kobayashi, T.2
Narasaka, K.3
-
13
-
-
0002089886
-
-
Kobayashi, T.; Koga, Y.; Narasaka, K. J. Organomet. Chem. 2001, 624, 73
-
(2001)
J. Organomet. Chem.
, vol.624
, pp. 73
-
-
Kobayashi, T.1
Koga, Y.2
Narasaka, K.3
-
14
-
-
38049085216
-
-
Wang, H.; Sawyer, J. R.; Evans, P. A.; Baik, M.-H. Angew. Chem., Int. Ed. 2008, 47, 342
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 342
-
-
Wang, H.1
Sawyer, J.R.2
Evans, P.A.3
Baik, M.-H.4
-
15
-
-
0033949371
-
-
Pagenkopf, B. L.; Belanger, D. B.; O?Mahony, D. J. R.; Livinghouse, T. Synthesis 2000, 1009
-
(2000)
Synthesis
, pp. 1009
-
-
Pagenkopf, B.L.1
Belanger, D.B.2
Omahony, D.J.R.3
Livinghouse, T.4
-
17
-
-
9144236440
-
-
For the challenges associated with conducting room-temperature PK reactions, see
-
For the challenges associated with conducting room-temperature PK reactions, see: Schmid, T. M.; Consiglio, G. Chem. Commun. 2004, 2318
-
(2004)
Chem. Commun.
, pp. 2318
-
-
Schmid, T.M.1
Consiglio, G.2
-
18
-
-
84986513567
-
-
We use the CHELP charges, as defined in
-
We use the CHELP charges, as defined in Breneman, C. M.; Wiberg, K. B. J. Comput. Chem. 1990, 11, 361
-
(1990)
J. Comput. Chem.
, vol.11
, pp. 361
-
-
Breneman, C.M.1
Wiberg, K.B.2
-
19
-
-
79957731679
-
-
See Supporting Information
-
See Supporting Information.
-
-
-
-
22
-
-
0345491105
-
-
Lee, C. T.; Yang, W. T.; Parr, R. G. Phys. Rev. B 1988, 37, 785
-
(1988)
Phys. Rev. B
, vol.37
, pp. 785
-
-
Lee, C.T.1
Yang, W.T.2
Parr, R.G.3
-
23
-
-
79957677367
-
-
The C4/C4′-positions are too close to the highly polarizable metal center to provide much information with regard to the electronic reorganization
-
The C4/C4′-positions are too close to the highly polarizable metal center to provide much information with regard to the electronic reorganization.
-
-
-
-
24
-
-
10044224654
-
-
For examples of metal-catalyzed [ m + n ] and [ m + n + o ] carbocyclizations with alkynyl halides, see the following. Ru [(2+2)]
-
For examples of metal-catalyzed [ m + n ] and [ m + n + o ] carbocyclizations with alkynyl halides, see the following. Ru [(2+2)]: Villenueve, K.; Riddell, N.; Jordan, R. W.; Tsui, G. C.; Tam, W. Org. Lett. 2004, 6, 4543
-
(2004)
Org. Lett.
, vol.6
, pp. 4543
-
-
Villenueve, K.1
Riddell, N.2
Jordan, R.W.3
Tsui, G.C.4
Tam, W.5
-
25
-
-
30144445489
-
-
Rh [(4+2)]
-
Rh [(4+2)]: Yoo, W.-J.; Allen, A.; Villeneuve, K.; Tam, W. Org. Lett. 2005, 7, 5853
-
(2005)
Org. Lett.
, vol.7
, pp. 5853
-
-
Yoo, W.-J.1
Allen, A.2
Villeneuve, K.3
Tam, W.4
-
26
-
-
70349906197
-
-
Ru [(2+2)+2]
-
Ru [(2+2)+2]: Nicolaou, K. C.; Tang, Y.; Wang, J. Angew. Chem., Int. Ed. 2009, 48, 3449
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 3449
-
-
Nicolaou, K.C.1
Tang, Y.2
Wang, J.3
|