-
1
-
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0003787433
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(Eds.), Pergamon, Exeter
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D. Barton, K. Nakanisky, O. Meth-Cohn (Eds.), Comprehensive Natural Products Chemistry, Pergamon, Exeter, 1999.
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(1999)
Comprehensive Natural Products Chemistry
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Barton, D.1
Nakanisky, K.2
Meth-Cohn, O.3
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2
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-
0003625966
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-
See, for instance: (Eds.), Pergamon, Oxford
-
See, for instance: E.W. Abel, F.G.A. Stone, G. Wilkinson (Eds.), Comprehensive Organometallic Chemistry II, Pergamon, Oxford, 1995.
-
(1995)
Comprehensive Organometallic Chemistry II
-
-
Abel, E.W.1
Stone, F.G.A.2
Wilkinson, G.3
-
3
-
-
0004114335
-
-
For two excellent monographs, see: (a) Wiley, New York
-
For two excellent monographs, see: (a) E.J. Corey, X.-M. Cheng, The logic of Chemical Synthesis, Wiley, New York, 1989
-
(1989)
The Logic of Chemical Synthesis
-
-
Corey, E.J.1
Cheng, X.-M.2
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8
-
-
0003391833
-
-
W.A. Herrmann (Ed.), G. Thieme Verlag, Stuttgar
-
R. Bartsach, C. Drost, U. Klingebiel, in: W.A. Herrmann (Ed.), Synthetic Methods of Organometallics and Inorganic Chemistry, G. Thieme Verlag, Stuttgar, 1996.
-
(1996)
Synthetic Methods of Organometallics and Inorganic Chemistry
-
-
Bartsach, R.1
Drost, C.2
Klingebiel, U.3
-
10
-
-
0030496093
-
For reviews on arene-catalysed reductive lithiation processes
-
see
-
For reviews on arene-catalysed reductive lithiation processes, see: M. Yus, Chem. Soc. Rev. 25 (1996) 155
-
(1996)
Chem. Soc. Rev.
, vol.25
, pp. 155
-
-
Yus, M.1
-
14
-
-
37049073704
-
For the first account on this process from our laboratory
-
see
-
For the first account on this process from our laboratory, see: M. Yus, D.J. Ramón, J. Chem. Soc. Chem. Commun. (1991) 398.
-
(1991)
J. Chem. Soc. Chem. Commun.
, pp. 398
-
-
Yus, M.1
Ramón, D.J.2
-
17
-
-
0032510282
-
For a polymer supported version of this reaction
-
see: (a)
-
For a polymer supported version of this reaction, see: (a) C. Gómez, S. Ruiz, M. Yus, Tetrahedron Lett. 39 (1998) 1397
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 1397
-
-
Gómez, C.1
Ruiz, S.2
Yus, M.3
-
20
-
-
0012669991
-
-
Other many uses of this methodology are: (a) Preparation of functionalised organolithium compounds [12] by chlorine- lithium exchange or reductive opening of heterocyles [13]
-
Other many uses of this methodology are: (a) Preparation of functionalised organolithium compounds [12] by chlorine- lithium exchange or reductive opening of heterocyles [13]
-
-
-
-
21
-
-
0012733527
-
-
Generation of organolithium reagents starting from nonhalogenated materials [14]
-
Generation of organolithium reagents starting from nonhalogenated materials [14]
-
-
-
-
22
-
-
0012623649
-
-
Activation of other metals [15]
-
Activation of other metals [15]
-
-
-
-
23
-
-
0012672237
-
-
Transmetallation process 7d
-
Transmetallation process 7d.
-
-
-
-
25
-
-
0002148313
-
-
E.W. Abel, F.G.A. Stone, G. Wilkinson (Eds.), Pergamon Press, Oxford
-
M. Gray, M. Tinkl, V. Snieckus, in: E.W. Abel, F.G.A. Stone, G. Wilkinson (Eds.), Comprehensive Organometallic Chemistry II, vol. 11, Pergamon Press, Oxford, 1995, p. 1;
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(1995)
Comprehensive Organometallic Chemistry II
, vol.11
, pp. 1
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-
Gray, M.1
Tinkl, M.2
Snieckus, V.3
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27
-
-
0034672069
-
-
A. Boudier, L.O. Bromm, M. Lozt, P. Knochel, Angew. Chem. Int. Ed. 39 (2000) 4414
-
(2000)
Angew. Chem. Int. Ed.
, vol.39
, pp. 4414
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-
Boudier, A.1
Bromm, L.O.2
Lozt, M.3
Knochel, P.4
-
31
-
-
0002364775
-
-
For a review, see
-
For a review, see: A. Guijarro, C. Gómez, M. Yus, Trends Org. Chem. 8 (2000) 65.
-
(2000)
Trends Org. Chem.
, vol.8
, pp. 65
-
-
Guijarro, A.1
Gómez, C.2
Yus, M.3
-
38
-
-
0032742950
-
-
For related systems, see: and literature quoted therein
-
For related systems, see: J. Ortiz, A. Guijarro, M. Yus, Eur. J. Org. Chem. (1999) 3005 and literature quoted therein.
-
(1999)
Eur. J. Org. Chem.
, pp. 3005
-
-
Ortiz, J.1
Guijarro, A.2
Yus, M.3
-
39
-
-
0035961108
-
-
Y. Hamashima, D. Sawada, H. Nogami, M. Kanai, M. Shibasaki, Tetrahedron 57 (2001) 805.
-
(2001)
Tetrahedron
, vol.57
, pp. 805
-
-
Hamashima, Y.1
Sawada, D.2
Nogami, H.3
Kanai, M.4
Shibasaki, M.5
-
40
-
-
33847797648
-
For leading references on bromine-lithium exchange using an alkyllithium as lithiation agent
-
see: (a)
-
For leading references on bromine-lithium exchange using an alkyllithium as lithiation agent, see: (a) W.E. Parham, L.D. Jones, Y.A. Sayed, J. Org. Chem. 41 (1976) 1184
-
(1976)
J. Org. Chem.
, vol.41
, pp. 1184
-
-
Parham, W.E.1
Jones, L.D.2
Sayed, Y.A.3
-
49
-
-
0034635617
-
For a recent application of this reaction in a similar process
-
see
-
For a recent application of this reaction in a similar process, see: T. Soler, A. Bachki, L.R. Falvello, F. Foubelo, M. Yus, Tetrahedron: Asymmetry 11 (2000) 493.
-
(2000)
Tetrahedron: Asymmetry
, vol.11
, pp. 493
-
-
Soler, T.1
Bachki, A.2
Falvello, L.R.3
Foubelo, F.4
Yus, M.5
-
50
-
-
0027168644
-
For a related synthesis of oxepanes
-
see
-
For a related synthesis of oxepanes, see: J.F. Gil, D.J. Ramón, M. Yus, Tetrahedron 49 (1993) 4923.
-
(1993)
Tetrahedron
, vol.49
, pp. 4923
-
-
Gil, J.F.1
Ramón, D.J.2
Yus, M.3
-
53
-
-
33845379418
-
-
For some examples, see: (a)
-
For some examples, see: (a) H. Yasuda, K. Kazuyuki, A. Nakamura, Acc. Chem. Res. 18 (1985) 120
-
(1985)
Acc. Chem. Res.
, vol.18
, pp. 120
-
-
Yasuda, H.1
Kazuyuki, K.2
Nakamura, A.3
-
57
-
-
0001181884
-
-
K. Mashima, H. Fukumoto, K. Tani, M.-A. Haga, A. Nakamura, Organometallics 17 (1998) 410
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(1998)
Organometallics
, vol.17
, pp. 410
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-
Mashima, K.1
Fukumoto, H.2
Tani, K.3
Haga, M.-A.4
Nakamura, A.5
-
58
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-
0035889198
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T.M. Cameron, I. Ghiviriga, K.A. Abboud, J.M. Boncella, Organometallics 20 (2001) 4378.
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(2001)
Organometallics
, vol.20
, pp. 4378
-
-
Cameron, T.M.1
Ghiviriga, I.2
Abboud, K.A.3
Boncella, J.M.4
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60
-
-
84987515768
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-
T. Imamoto, T. Yoshizawa, K. Hirose, Y. Wada, H. Masuda, K. Yamaguchi, H. Seki, Heteroatom. Chem. 6 (1995) 99.
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(1995)
Heteroatom. Chem.
, vol.6
, pp. 99
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-
Imamoto, T.1
Yoshizawa, T.2
Hirose, K.3
Wada, Y.4
Masuda, H.5
Yamaguchi, K.6
Seki, H.7
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