-
10
-
-
33845277870
-
-
For recent examples of silicon-based cross-coupling, see: (a) Y. Hatanaka, and T. Hiyama J. Org. Chem. 53 1988 918
-
(1988)
J. Org. Chem.
, vol.53
, pp. 918
-
-
Hatanaka, Y.1
Hiyama, T.2
-
15
-
-
0034625934
-
-
P.Y.S. Lam, S. Deudon, K.M. Averill, R. Li, M. He, P. DeShong, and C.G. Lark J. Am. Chem. Soc. 122 2000 7600
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 7600
-
-
Lam, P.Y.S.1
Deudon, S.2
Averill, K.M.3
Li, R.4
He, M.5
Deshong, P.6
Lark, C.G.7
-
16
-
-
0000581101
-
-
K. Hirabayashi, J. Kawashima, Y. Nishihara, A. Mori, and T. Hayama Org. Lett. 1 1999 299
-
(1999)
Org. Lett.
, vol.1
, pp. 299
-
-
Hirabayashi, K.1
Kawashima, J.2
Nishihara, Y.3
Mori, A.4
Hayama, T.5
-
17
-
-
0034068081
-
-
K. Hirabayashi, T. Kondo, F. Toriyama, Y. Nishihara, and A. Mori Bull. Chem. Soc. Jpn 73 2000 749
-
(2000)
Bull. Chem. Soc. Jpn
, vol.73
, pp. 749
-
-
Hirabayashi, K.1
Kondo, T.2
Toriyama, F.3
Nishihara, Y.4
Mori, A.5
-
37
-
-
0034045753
-
-
K. Hirabayashi, J.-i. Ando, J. Kawashima, Y. Nishihara, A. Mori, and T. Hiyama Bull. Chem. Soc. Jpn 73 2000 1409
-
(2000)
Bull. Chem. Soc. Jpn
, vol.73
, pp. 1409
-
-
Hirabayashi, K.1
Ando, J.I.2
Kawashima, J.3
Nishihara, Y.4
Mori, A.5
Hiyama, T.6
-
38
-
-
0032374573
-
-
A. Mori, E. Takahisa, H. Kajiro, K. Hirabayashi, Y. Nishihara, and T. Hiyama Chem. Lett. 1998 443
-
(1998)
Chem. Lett.
, pp. 443
-
-
Mori, A.1
Takahisa, E.2
Kajiro, H.3
Hirabayashi, K.4
Nishihara, Y.5
Hiyama, T.6
-
39
-
-
0042152046
-
-
M. Murata, M. Ishikura, M. Nagata, S. Watanabe, and Y. Masuda Org. Lett. 4 2002 1843
-
(2002)
Org. Lett.
, vol.4
, pp. 1843
-
-
Murata, M.1
Ishikura, M.2
Nagata, M.3
Watanabe, S.4
Masuda, Y.5
-
64
-
-
0033568351
-
-
S.S. Zhu, D.R. Cefalo, D.S. La, J.Y. Jamieson, W.M. Davis, A.H. Hoveyda, and R.R. Schrock J. Am. Chem. Soc. 121 1999 8251
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 8251
-
-
Zhu, S.S.1
Cefalo, D.R.2
La, D.S.3
Jamieson, J.Y.4
Davis, W.M.5
Hoveyda, A.H.6
Schrock, R.R.7
-
65
-
-
0035901680
-
-
S.L. Aeilts, D.R. Cefalo, P.J. Bonitatebus Jr., J.H. Houser, A.H. Hoveyda, and R.R. Schrock Angew. Chem. Int. Ed. 40 2001 1452
-
(2001)
Angew. Chem. Int. Ed.
, vol.40
, pp. 1452
-
-
Aeilts, S.L.1
Cefalo, D.R.2
Bonitatebus Jr., P.J.3
Houser, J.H.4
Hoveyda, A.H.5
Schrock, R.R.6
-
66
-
-
0034598054
-
-
G.S. Weatherhead, J.H. Houser, J.G. Ford, J.Y. Jamieson, R.R. Schrock, and A.H. Hoveyda Tetrahedron Lett. 41 2000 9553
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 9553
-
-
Weatherhead, G.S.1
Houser, J.H.2
Ford, J.G.3
Jamieson, J.Y.4
Schrock, R.R.5
Hoveyda, A.H.6
-
73
-
-
0033104447
-
-
M. Ahmed, A.G.M. Barrett, J.C. Beall, D.C. Braddock, K. Flack, V.C. Gibson, P.A. Procopiou, and M.M. Salter Tetrahedron 55 1999 3219
-
(1999)
Tetrahedron
, vol.55
, pp. 3219
-
-
Ahmed, M.1
Barrett, A.G.M.2
Beall, J.C.3
Braddock, D.C.4
Flack, K.5
Gibson, V.C.6
Procopiou, P.A.7
Salter, M.M.8
-
74
-
-
0034613158
-
-
A.G.M. Barrett, J.C. Beall, D.C. Braddock, K. Flack, V.C. Gibson, and M.M. Salter J. Org. Chem. 65 2000 6508
-
(2000)
J. Org. Chem.
, vol.65
, pp. 6508
-
-
Barrett, A.G.M.1
Beall, J.C.2
Braddock, D.C.3
Flack, K.4
Gibson, V.C.5
Salter, M.M.6
-
76
-
-
0001101871
-
-
(e) The ruthenium carbene complex 1 is more sensitive to the substitution pattern of alkenes than molybdenum catalyst 3, see: T.A. Kirkland, and R.H. Grubbs J. Org. Chem. 62 1997 7310
-
(1997)
J. Org. Chem.
, vol.62
, pp. 7310
-
-
Kirkland, T.A.1
Grubbs, R.H.2
-
77
-
-
0034246704
-
-
L. Yet Chem. Rev. 100 2000 2963
-
(2000)
Chem. Rev.
, vol.100
, pp. 2963
-
-
Yet, L.1
-
87
-
-
0001427904
-
-
For the construction of a 10-membered ring diene with one exo double bond, see: (b) D.H. Hodgson, A.M. Foley, L.T. Boulton, P.J. Lovell, and G.N. Maw J. Chem. Soc., Perkin Trans. 1 1999 2911
-
(1999)
J. Chem. Soc., Perkin Trans. 1
, pp. 2911
-
-
Hodgson, D.H.1
Foley, A.M.2
Boulton, L.T.3
Lovell, P.J.4
Maw, G.N.5
-
88
-
-
0001071834
-
-
Portions of this work have been communicated previously: (a) S.E. Denmark, and S.-M. Yang Org. Lett. 3 2001 1749
-
(2001)
Org. Lett.
, vol.3
, pp. 1749
-
-
Denmark, S.E.1
Yang, S.-M.2
-
90
-
-
0001384547
-
-
Some specific examples on medium-sized ring formation with diene unit, see: (a) S. Ma, and E. Negishi J. Am. Chem. Soc. 117 1995 6345
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 6345
-
-
Ma, S.1
Negishi, E.2
-
94
-
-
0033598258
-
-
Recently, the 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene-substituted ruthenium complex exhibited high reactivity in RCM, especially for di-, tri- or tetra-substituted cyclic alkenes, see: M. Scholl, S. Ding, C.W. Lee, and R.H. Grubbs Org. Lett. 1 1999 953
-
(1999)
Org. Lett.
, vol.1
, pp. 953
-
-
Scholl, M.1
Ding, S.2
Lee, C.W.3
Grubbs, R.H.4
-
95
-
-
33751392358
-
-
The molybdenum complex
-
The molybdenum complex 3 is commercially available (Strem) and can be prepared according to a reported procedure with consistent purity and reactivity, see: (a) H.H. Fox, K.B. Yap, J. Robbins, S. Cai, and R.R. Schrock Inorg. Chem. 31 1992 2287
-
(1992)
Inorg. Chem.
, vol.31
, pp. 2287
-
-
Fox, H.H.1
Yap, K.B.2
Robbins, J.3
Cai, S.4
Schrock, R.R.5
-
96
-
-
0001077422
-
-
R.R. Schrock, J.S. Murdzek, G.C. Bazan, J. Robbins, M. DiMare, and M. O'Regan J. Am. Chem. Soc. 112 1990 3875
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 3875
-
-
Schrock, R.R.1
Murdzek, J.S.2
Bazan, G.C.3
Robbins, J.4
Dimare, M.5
O'Regan, M.6
-
97
-
-
0000334943
-
-
J.H. Oskam, H.H. Fox, K.B. Yap, D.H. McConville, R. O'Dell, B.J. Lichtenstein, and R.R. Schrock J. Organomet. Chem. 459 1993 185
-
(1993)
J. Organomet. Chem.
, vol.459
, pp. 185
-
-
Oskam, J.H.1
Fox, H.H.2
Yap, K.B.3
McConville, D.H.4
O'Dell, R.5
Lichtenstein, B.J.6
Schrock, R.R.7
-
101
-
-
0000359232
-
-
P.J. Scheuer Academic New York
-
K.L. Erickson P.J. Scheuer Marine Natural Products Vol. 5 1983 Academic New York 131 257
-
(1983)
Marine Natural Products
, vol.5
, pp. 131-257
-
-
Erickson, K.L.1
-
103
-
-
0032510406
-
-
Isobe et al. have reported the construction of medium ring ethers (7-10 rings) with an internal 1,3-diene unit through cyclization of an acetylene cobalt complex followed by reductive decomplexation. (a) C. Yenjai, and M. Isobe Tetrahedron 54 1998 2509
-
(1998)
Tetrahedron
, vol.54
, pp. 2509
-
-
Yenjai, C.1
Isobe, M.2
-
106
-
-
0001354464
-
-
Alkylidene 1 has been shown to react with acetylenic halides through halide exchange. Vinyl halide containing dienes were also failed to cyclize using either 1 or Mo-complex 3, (a) S.-H. Kim, W.J. Zuercher, N.B. Bowden, and R.H. Grubbs J. Org. Chem. 61 1996 1073
-
(1996)
J. Org. Chem.
, vol.61
, pp. 1073
-
-
Kim, S.-H.1
Zuercher, W.J.2
Bowden, N.B.3
Grubbs, R.H.4
-
107
-
-
0141854289
-
-
(b) A successful RCM of vinyl chloride was disclosed recently, see: W. Chao, and S.M. Weinreb Org. Lett. 5 2003 2505
-
(2003)
Org. Lett.
, vol.5
, pp. 2505
-
-
Chao, W.1
Weinreb, S.M.2
-
109
-
-
0034731535
-
-
J. Wagner, L.M.M. Cabrejas, C.E. Grossmith, C. Papagerogiou, F. Senia, D. Wagner, J. France, and S.P. Nolan J. Org. Chem. 65 2000 9255
-
(2000)
J. Org. Chem.
, vol.65
, pp. 9255
-
-
Wagner, J.1
Cabrejas, L.M.M.2
Grossmith, C.E.3
Papagerogiou, C.4
Senia, F.5
Wagner, D.6
France, J.7
Nolan, S.P.8
-
110
-
-
0034595258
-
-
C.A. Dvorak, W.D. Schmitz, D.J. Poon, D.C. Pryde, J.P. Lawson, R.A. Amos, and A.I. Meyers Angew. Chem. Int. Ed. 39 2000 1664
-
(2000)
Angew. Chem. Int. Ed.
, vol.39
, pp. 1664
-
-
Dvorak, C.A.1
Schmitz, W.D.2
Poon, D.J.3
Pryde, D.C.4
Lawson, J.P.5
Amos, R.A.6
Meyers, A.I.7
-
111
-
-
0037613530
-
-
For an example of formation of a marocyclic triene by RCM of a tetraene see: (a) X. Wang, and J.A. Porco Jr. J. Am. Chem. Soc. 125 2003 6040
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 6040
-
-
Wang, X.1
Porco Jr., J.A.2
-
114
-
-
0034674322
-
-
(a) Conformational constraints have a dramatic effect on the success of ring closure. For a recent review on synthesis of medium rings using RCM strategies, see: M.E. Maier Angew. Chem. Int. Ed. 39 2000 2073
-
(2000)
Angew. Chem. Int. Ed.
, vol.39
, pp. 2073
-
-
Maier, M.E.1
-
116
-
-
85081438957
-
-
An attempt to promote closure of simple acyclic dienes to 8-membered carbocycles with Ru-complex 1 met with failure, see Ref. 12e
-
An attempt to promote closure of simple acyclic dienes to 8-membered carbocycles with Ru-complex 1 met with failure, see Ref. 12e
-
-
-
-
117
-
-
0010616713
-
-
It has been proposed that the palladium catalyst could act as a template to coordinate both ends of the molecule through oxidative addition followed by coordination of the organostannane in intramolecular Stille couplings. J.K. Stille, and M. Tanaka J. Am. Chem. Soc. 109 1987 3785
-
(1987)
J. Am. Chem. Soc.
, vol.109
, pp. 3785
-
-
Stille, J.K.1
Tanaka, M.2
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