-
6
-
-
0033591863
-
-
(a) Evans, P.A., Robinson, J.E., Nelson, J.D. J. Am. Chem. Soc. 1999, 121, 6761, 12214;
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 6761
-
-
Evans, P.A.1
Robinson, J.E.2
Nelson, J.D.3
-
8
-
-
0035909588
-
-
(c) Evans, P.A., Robinson, J.E., Moffett, K.K. Org. Lett. 2001, 3, 3269.
-
(2001)
Org. Lett.
, vol.3
, pp. 3269
-
-
Evans, P.A.1
Robinson, J.E.2
Moffett, K.K.3
-
11
-
-
0037205927
-
-
Evans, P.A., Robinson, J.E., Baum, E.W., Fazal, A.N. J. Am. Chem. Soc. 2002, 124, 8782.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 8782
-
-
Evans, P.A.1
Robinson, J.E.2
Baum, E.W.3
Fazal, A.N.4
-
13
-
-
0000969879
-
-
Wiley: New York, ch. 4
-
For book chapters on metal-catalyzed allylic substitution, see: (a) Tsuji, J. In Palladium Reagents and Catalysts, Wiley: New York, 1996, ch. 4, pp. 290-404;
-
(1996)
Palladium Reagents and Catalysts
, pp. 290-404
-
-
Tsuji, J.1
-
14
-
-
0002177913
-
-
Ojima, I., ed., Wiley-VCH: New York, ch. 8
-
(b) Trost, B.M., Lee, C. In Catalytic Asymmetric Synthesis, 2nd ed., Ojima, I., ed., Wiley-VCH: New York, 2000, ch. 8, pp. 593-649.
-
(2000)
Catalytic Asymmetric Synthesis, 2nd Ed.
, pp. 593-649
-
-
Trost, B.M.1
Lee, C.2
-
15
-
-
0027380506
-
-
For lead references on other transition metal-catalyzed allylic alkylation reactions, see: (a) Co: Bhatia, B., Reddy, M.M., Iqbal, J. Tetrahedron Lett. 1993, 34, 6301;
-
(1993)
Tetrahedron Lett.
, vol.34
, pp. 6301
-
-
Bhatia, B.1
Reddy, M.M.2
Iqbal, J.3
-
19
-
-
0000596906
-
-
(e) Mo: Ward, Y.D., Villanueva, L.A., Allred, G.D., Liebeskind, L.S. J. Am. Chem. Soc. 1996, 118, 897;
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 897
-
-
Ward, Y.D.1
Villanueva, L.A.2
Allred, G.D.3
Liebeskind, L.S.4
-
20
-
-
4143055609
-
-
(f) Ni: Bricout, H., Carpentier, J.-F., Mortreux, A. J. Chem. Soc. Chem. Commun. 1995, 1863;
-
(1995)
J. Chem. Soc. Chem. Commun.
, pp. 1863
-
-
Bricout, H.1
Carpentier, J.-F.2
Mortreux, A.3
-
22
-
-
0037087753
-
-
(h) Ru: Trost, B.M., Fraisse, P.L., Ball, Z.T. Angew. Chem. Int. Ed. Engl. 2002, 41, 1059;
-
(2002)
Angew. Chem. Int. Ed. Engl.
, vol.41
, pp. 1059
-
-
Trost, B.M.1
Fraisse, P.L.2
Ball, Z.T.3
-
26
-
-
0034823238
-
-
(c) You, S.-L., Zhu, X.-Z., Luo, Y.-M., Hou, X.-L., Dai, L.-X. J. Am. Chem. Soc. 2001, 123, 7471;
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 7471
-
-
You, S.-L.1
Zhu, X.-Z.2
Luo, Y.-M.3
Hou, X.-L.4
Dai, L.-X.5
-
27
-
-
0242500920
-
-
(d) Lopez, F., Ohmura, T., Hartwig, J.F. J. Am. Chem. Soc. 2003, 125, 3426;
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 3426
-
-
Lopez, F.1
Ohmura, T.2
Hartwig, J.F.3
-
28
-
-
0141518172
-
-
(e) Hayashi, T., Okada, A., Suzuka, T., Kawatsura, M. Org. Lett. 2003, 5, 1713.
-
(2003)
Org. Lett.
, vol.5
, pp. 1713
-
-
Hayashi, T.1
Okada, A.2
Suzuka, T.3
Kawatsura, M.4
-
29
-
-
0001124147
-
-
Hayashi, T., Yamamoto, A., Hagihara, T. J. Org. Chem. 1986, 51, 723.
-
(1986)
J. Org. Chem.
, vol.51
, pp. 723
-
-
Hayashi, T.1
Yamamoto, A.2
Hagihara, T.3
-
30
-
-
0000803558
-
-
(a) Tsuji, J., Minami, I., Shimizu, I. Tetrahedron Lett. 1984, 25, 5157;
-
(1984)
Tetrahedron Lett.
, vol.25
, pp. 5157
-
-
Tsuji, J.1
Minami, I.2
Shimizu, I.3
-
31
-
-
0000213281
-
-
(b) Minami, I., Shimizu, I., Tsuji, J. J. Organometallic Chem. 1985, 296, 269.
-
(1985)
Organometallic Chem.
, vol.296
, pp. 269
-
-
Minami, I.1
Shimizu, I.2
Tsuji, J.J.3
-
32
-
-
0000849837
-
-
For related examples of rhodium-catalyzed allylic substitution reactions, see: (a) Takeuchi, R., Kitamura, N. New. J. Chem. 1998, 659;
-
(1998)
New. J. Chem.
, pp. 659
-
-
Takeuchi, R.1
Kitamura, N.2
-
33
-
-
0012543140
-
-
pertinent references therein
-
(b) Fagnou, K., Lautens, M. Org. Lett. 2000, 2, 2319 and pertinent references therein.
-
(2000)
Org. Lett.
, vol.2
, pp. 2319
-
-
Fagnou, K.1
Lautens, M.2
-
34
-
-
0001528563
-
-
Abel, E.W., Stone, F.G.A., Wilkinson, G., eds., Pergamon Press: New York, ch. 2
-
Enyl complexes are, by definition, those that have a discrete σ- and π-metal carbon component within a single ligand. Sharp, P.R. In Comprehensive Organometallic Chemistry II, Abel, E.W., Stone, F.G.A., Wilkinson, G., eds., Pergamon Press: New York, 1995, ch. 2, p. 272.
-
(1995)
Comprehensive Organometallic Chemistry II
, pp. 272
-
-
Sharp, P.R.1
-
35
-
-
0005568365
-
-
Tanaka, I., Jin-no, N., Kushida, T., Tsutsui, N., Ashida, T., Suzuki, H., Sakurai, H., Moro-oka, Y., Ikawa, T. Bull. Chem. Soc. Jpn. 1983, 56, 657.
-
(1983)
Bull. Chem. Soc. Jpn.
, vol.56
, pp. 657
-
-
Tanaka, I.1
Jin-no, N.2
Kushida, T.3
Tsutsui, N.4
Ashida, T.5
Suzuki, H.6
Sakurai, H.7
Moro-oka, Y.8
Ikawa, T.9
-
36
-
-
0242558426
-
-
note
-
The term conservation of enantiomeric excess {cee = (product ee/starting material ee) × 100} provides a convenient method of describing the enantiospecificity of the reaction.
-
-
-
-
39
-
-
0344006321
-
-
pertinent references cited therein
-
For a recent review on ring-closing metathesis, see: Fürstner, A. Angew. Chem. Int. Ed. 2000, 39, 3012 and pertinent references cited therein.
-
(2000)
Angew. Chem. Int. Ed.
, vol.39
, pp. 3012
-
-
Fürstner, A.1
-
40
-
-
4243987144
-
-
For a recent review on allylic amination, see: Johannsen, M., Jørgensen, K.A. Chem. Rev. 1998, 98, 1689.
-
(1998)
Chem. Rev.
, vol.98
, pp. 1689
-
-
Johannsen, M.1
Jørgensen, K.A.2
-
41
-
-
0033598258
-
-
Scholl, M., Ding, S., Lee, C.W., Grubbs, R.H. Org. Lett. 1999, 1, 953.
-
(1999)
Org. Lett.
, vol.1
, pp. 953
-
-
Scholl, M.1
Ding, S.2
Lee, C.W.3
Grubbs, R.H.4
-
42
-
-
0037016413
-
-
For a recent review on halide effects in transition metal catalysis, see: Fagnou, K., Lautens, M. Angew. Chem. Int. Ed. 2002, 41, 26.
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, pp. 26
-
-
Fagnou, K.1
Lautens, M.2
-
43
-
-
0000463815
-
-
(a) Ojima, I., Tzamarioudaki, M., Li, Z., Donavan, R.J. Chem. Rev. 1996, 96, 635;
-
(1996)
Chem. Rev.
, vol.96
, pp. 635
-
-
Ojima, I.1
Tzamarioudaki, M.2
Li, Z.3
Donavan, R.J.4
-
44
-
-
0036522941
-
-
(b) Aubert, C., Buisine, O., Malacria, M. Chem. Rev. 2002, 102, 813.
-
(2002)
Chem. Rev.
, vol.102
, pp. 813
-
-
Aubert, C.1
Buisine, O.2
Malacria, M.3
-
45
-
-
0000330557
-
-
For recent reviews on metal-mediated cyclooctanoid construction, see: (a) Mehta, G., Singh, V. Chem. Rev. 1999, 99, 881;
-
(1999)
Chem. Rev.
, vol.99
, pp. 881
-
-
Mehta, G.1
Singh, V.2
-
46
-
-
0034246704
-
-
(b) Yet, L. Chem. Rev. 2000, 100, 2963.
-
(2000)
Chem. Rev.
, vol.100
, pp. 2963
-
-
Yet, L.1
-
47
-
-
0037181346
-
-
For related transition metal-catalyzed carbocyclizations leading to 8-membered rings, see: (a) Wender, P.A., Gamber, G.G., Hubbard, R.D., Zhang, L. J. Am. Chem. Soc. 2002, 124, 2876;
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 2876
-
-
Wender, P.A.1
Gamber, G.G.2
Hubbard, R.D.3
Zhang, L.4
-
49
-
-
0034601016
-
-
The rhodium-catalyzed cycloisomerization of 1,3-butadiene is known to favor oligomerization rather than the formation of cyclooctadiene, see: Bosch, M., Brookhart, M.S., Ilg, K., Werner, H. Angew Chem. Int. Ed. 2000, 39, 2304.
-
(2000)
Angew Chem. Int. Ed.
, vol.39
, pp. 2304
-
-
Bosch, M.1
Brookhart, M.S.2
Ilg, K.3
Werner, H.4
-
50
-
-
0242643109
-
-
note
-
The stereochemistry of the major diastereoisomer was reassigned based on a recent X-ray crystal structure. The rather unusual eight-membered ring conformation forces the protons pseudo-equational explaining the observed NOE enhancement (5.2%), despite their trans-relationship.
-
-
-
-
51
-
-
0034686072
-
-
For a recent review on the Pauson-Khand reaction, see: Brummond, K.M., Kent, J.L. Tetrahedron 2000, 56, 3263.
-
(2000)
Tetrahedron
, vol.56
, pp. 3263
-
-
Brummond, K.M.1
Kent, J.L.2
-
52
-
-
0034684229
-
-
For a related tandem allylic alkylation/Pauson-Khand carbocyclization, see: Jeong, N., Seo, S.-D., Shin, J.-Y. J. Am. Chem. Soc. 2000, 122, 10220.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 10220
-
-
Jeong, N.1
Seo, S.-D.2
Shin, J.-Y.3
|