-
4
-
-
0037503118
-
-
(Eds.: Z. Rappoport, I. Marek), Wiley, New York
-
The Chemistry of Organolithium Compounds, Part 2 (Eds.:, Z. Rappoport, I. Marek,), Wiley, New York, 2004.
-
(2004)
The Chemistry of Organolithium Compounds, Part 2
-
-
-
6
-
-
0001269629
-
-
For a seminal review of donor effects on lithium enolate aggregation, see
-
For a seminal review of donor effects on lithium enolate aggregation, see:, D. Seebach, Angew. Chem. 1988, 100, 1685
-
(1988)
Angew. Chem.
, vol.100
, pp. 1685
-
-
Seebach, D.1
-
8
-
-
0035312375
-
-
B. Walfort, L. Lameyer, W. Weiss, R. Herbst-Irmer, R. Bertermann, J. Rocha, D. Stalke, Chem. Eur. J. 2001, 7, 1417.
-
(2001)
Chem. Eur. J.
, vol.7
, pp. 1417
-
-
Walfort, B.1
Lameyer, L.2
Weiss, W.3
Herbst-Irmer, R.4
Bertermann, R.5
Rocha, J.6
Stalke, D.7
-
11
-
-
36048944800
-
-
D. Bojer, I. Kamps, X. Tian, A. Hepp, T. Pape, R. Fröhlich, N. W. Mitzel, Angew. Chem. 2007, 119, 4254
-
(2007)
Angew. Chem.
, vol.119
, pp. 4254
-
-
Bojer, D.1
Kamps, I.2
Tian, X.3
Hepp, A.4
Pape, T.5
Fröhlich, R.6
Mitzel, N.W.7
-
13
-
-
78149352182
-
-
4746
-
I. Kamps, B. Neumann, H.-G. Stammler, N. W. Mitzel, Organometallics 2010, 29, 4746.
-
(2010)
Organometallics
, pp. 29
-
-
Kamps, I.1
Neumann, B.2
Stammler, H.-G.3
Mitzel, N.W.4
-
14
-
-
49849115926
-
-
MeLi forms a tetrameric heterocubane, which is linked to other heterocubanes in three dimensions by weak Li⋯Me interactions
-
MeLi forms a tetrameric heterocubane, which is linked to other heterocubanes in three dimensions by weak Li⋯Me interactions:, E. Weiss, G. Hencken, J. Organomet. Chem. 1970, 21, 265.
-
(1970)
J. Organomet. Chem.
, vol.21
, pp. 265
-
-
Weiss, E.1
Hencken, G.2
-
16
-
-
46149131343
-
-
B. Tecle, A. F. M. M. Rahman, J. P. Oliver, J. Organomet. Chem. 1986, 317, 267.
-
(1986)
J. Organomet. Chem.
, vol.317
, pp. 267
-
-
Tecle, B.1
Rahman, A.F.M.M.2
Oliver, J.P.3
-
17
-
-
67650607746
-
-
W. Clegg, B. Conway, D. V. Graham, E. Hevia, A. R. Kennedy, R. E. Mulvey, L. Russo, D. S. Wright, Chem. Eur. J. 2009, 15, 7074.
-
(2009)
Chem. Eur. J.
, vol.15
, pp. 7074
-
-
Clegg, W.1
Conway, B.2
Graham, D.V.3
Hevia, E.4
Kennedy, A.R.5
Mulvey, R.E.6
Russo, L.7
Wright, D.S.8
-
18
-
-
33746967868
-
-
For an outstanding review of the structural chemistry of organolithium compounds, see
-
For an outstanding review of the structural chemistry of organolithium compounds, see:, W. N. Setzer, P. von R. Schleyer, Adv. Organomet. Chem. 1985, 24, 353.
-
(1985)
Adv. Organomet. Chem.
, vol.24
, pp. 353
-
-
Setzer, W.N.1
Schleyer, P.V.R.2
-
19
-
-
77956754782
-
-
The structural chemistry of the organo complexes of the heavier alkali metals has also received a comprehensive treatise
-
The structural chemistry of the organo complexes of the heavier alkali metals has also received a comprehensive treatise:, C. Schade, P. von R. Schleyer, Adv. Organomet. Chem. 1987, 27, 169.
-
(1987)
Adv. Organomet. Chem.
, vol.27
, pp. 169
-
-
Schade, C.1
Schleyer, P.V.R.2
-
21
-
-
0034669321
-
-
4] (M=Na, K, Rb, Cs) are isomeric
-
4] (M=Na, K, Rb, Cs) are isomeric:, D. R. Armstrong, W. Clegg, A. M. Drummond, S. T. Liddle, R. E. Mulvey, J. Am. Chem. Soc. 2000, 122, 11117.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 11117
-
-
Armstrong, D.R.1
Clegg, W.2
Drummond, A.M.3
Liddle, S.T.4
Mulvey, R.E.5
-
22
-
-
0036025593
-
-
J. Arnold, V. Knapp, J. A. R. Schmidt, A. Shafir, J. Chem. Soc. Dalton Trans. 2002, 3273.
-
(2002)
J. Chem. Soc. Dalton Trans.
, pp. 3273
-
-
Arnold, J.1
Knapp, V.2
Schmidt, J.A.R.3
Shafir, A.4
-
23
-
-
84985668655
-
-
W. Zarges, M. Marsch, K. Harms, G. Boche, Chem. Ber. 1989, 122, 2303.
-
(1989)
Chem. Ber.
, vol.122
, pp. 2303
-
-
Zarges, W.1
Marsch, M.2
Harms, K.3
Boche, G.4
-
25
-
-
0000182336
-
-
D. R. Baker, W. Clegg, L. Horsburgh, R. E. Mulvey, Organometallics 1994, 13, 4170).
-
(1994)
Organometallics
, vol.13
, pp. 4170
-
-
Baker, D.R.1
Clegg, W.2
Horsburgh, L.3
Mulvey, R.E.4
-
26
-
-
79952381053
-
-
3CK·PMDETA (PMDETA=N,N,N′,N′′,N′′- pentamethyldiethylenetriamine) is a polymer [
-
3CK·PMDETA (PMDETA=N,N,N′,N′′,N′′- pentamethyldiethylenetriamine) is a polymer [
-
-
-
-
28
-
-
0001414305
-
-
D. Hoffmann, W. Bauer, P. von R. Schleyer, U. Pieper, D. Stalke, Organometallics 1993, 12, 1193 ].
-
(1993)
Organometallics
, vol.12
, pp. 1193
-
-
Hoffmann, D.1
Bauer, W.2
Schleyer, P.V.R.3
Pieper, U.4
Stalke, D.5
-
30
-
-
0033434840
-
-
C. Slugovcl, C. Gemel, J.-Y. Shen, D. Doberer, R. Schmid, K. Kirchner, K. Mereiter, Monatsh. Chem. 1999, 130, 363
-
(1999)
Monatsh. Chem.
, vol.130
, pp. 363
-
-
Slugovcl, C.1
Gemel, C.2
Shen, J.-Y.3
Doberer, D.4
Schmid, R.5
Kirchner, K.6
Mereiter, K.7
-
31
-
-
79952415233
-
-
D. M. Cousins, M. G. Davidson, C. J. Frankis, D. García- Vivõ, M. F. Mahon, Dalton Trans. 2010, 39.
-
(2010)
Dalton Trans.
, pp. 39
-
-
Cousins, D.M.1
Davidson, M.G.2
Frankis, C.J.3
García-Vivõ, D.4
Mahon, M.F.5
-
32
-
-
0030814711
-
-
3 fashion although no structural evidence was presented
-
3 fashion although no structural evidence was presented:, H. Luitjes, M. Schakel, M. P. Aarnts, R. F. Schmitz, F. J. J. deKanter, G. W. Klumpp, Tetrahedron 1997, 53, 9977.
-
(1997)
Tetrahedron
, vol.53
, pp. 9977
-
-
Luitjes, H.1
Schakel, M.2
Aarnts, M.P.3
Schmitz, R.F.4
Dekanter, F.J.J.5
Klumpp, G.W.6
-
33
-
-
11044220836
-
-
For a review of tripodal tetraamine ligands, see
-
For a review of tripodal tetraamine ligands, see:, A. G. Blackman, Polyhedron 2005, 24, 1.
-
(2005)
Polyhedron
, vol.24
, pp. 1
-
-
Blackman, A.G.1
-
34
-
-
27744459829
-
-
6TREN, see
-
6TREN, see:, G. J. P. Britovsek, J. England, A. J. P. White, Inorg. Chem. 2005, 44, 8125.
-
(2005)
Inorg. Chem.
, vol.44
, pp. 8125
-
-
Britovsek, G.J.P.1
England, J.2
White, A.J.P.3
-
35
-
-
0001386975
-
-
1HNMR spectrum after 16h. For an illuminating review containing examples of heteroatom(TMEDA)-induced metallations, see
-
1HNMR spectrum after 16h. For an illuminating review containing examples of heteroatom(TMEDA)-induced metallations, see:, D. B. Collum, Acc. Chem. Res. 1992, 25, 448.
-
(1992)
Acc. Chem. Res.
, vol.25
, pp. 448
-
-
Collum, D.B.1
-
36
-
-
79952368299
-
-
note
-
-3. CCDC-790265 (1), CCDC-790266 (2), and CCDC-790267 (3) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.
-
-
-
-
37
-
-
0040649305
-
-
4 fashion to LiI although this is not a suitable ligand for organo-alkali metal complexes due to the high CH acidity of the ligand backbone
-
4 fashion to LiI although this is not a suitable ligand for organo-alkali metal complexes due to the high CH acidity of the ligand backbone:, S. K. Brownstein, P.-Y. Plouffe, C. Bensimon, J. Tse, Inorg. Chem. 1994, 33, 354.
-
(1994)
Inorg. Chem.
, vol.33
, pp. 354
-
-
Brownstein, S.K.1
Plouffe, P.-Y.2
Bensimon, C.3
Tse, J.4
-
38
-
-
33947294592
-
-
S. P. Patterman, I. L. Karle, G. D. Stucky, J. Am. Chem. Soc. 1970, 92, 1150.
-
(1970)
J. Am. Chem. Soc.
, vol.92
, pp. 1150
-
-
Patterman, S.P.1
Karle, I.L.2
Stucky, G.D.3
-
42
-
-
12044254104
-
-
D. Hoffmann, W. Bauer, F. Hampel, N. J. R. van Eikema Hommes, P. von R. Schleyer, P. Otto, U. Pieper, D. Stalke, D. S. Wright, R. Snaith, J. Am. Chem. Soc. 1994, 116, 528.
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 528
-
-
Hoffmann, D.1
Bauer, W.2
Hampel, F.3
Hommes, N.J.R.V.E.4
Schleyer, P.V.R.5
Otto, P.6
Pieper, U.7
Stalke, D.8
Wright, D.S.9
Snaith, R.10
-
46
-
-
33744479488
-
-
H. Schumann, D. M. M. Freckmann, S. Dechert, Organometallics 2006, 25, 2696.
-
(2006)
Organometallics
, vol.25
, pp. 2696
-
-
Schumann, H.1
Freckmann, D.M.M.2
Dechert, S.3
-
47
-
-
41049087106
-
-
S. Harder, C. Ruspic, N. Ní Bhriain, F. Berkermann, M. Schürmann, Z. Naturforsch. B 2008, 63, 267
-
(2008)
Z. Naturforsch. B
, vol.63
, pp. 267
-
-
Harder, S.1
Ruspic, C.2
Bhriain, N.N.3
Berkermann, F.4
Schürmann, M.5
-
49
-
-
0001617965
-
-
For a review of the effect of alkali metal identity on "carbanions", see
-
For a review of the effect of alkali metal identity on "carbanions", see:, C. Lambert, P. von R. Schleyer, Angew. Chem. 1994, 106, 1187
-
(1994)
Angew. Chem.
, vol.106
, pp. 1187
-
-
Lambert, C.1
Schleyer, P.V.R.2
-
51
-
-
79952386491
-
-
2 group is sufficiently isolated for such satellites to be visible in a strong sample
-
2 group is sufficiently isolated for such satellites to be visible in a strong sample.
-
-
-
-
52
-
-
0001588585
-
-
W=368.51amu)
-
W=368.51amu) :, S. Neander, F. E. Tio, R. Buschmann, U. Behrens, F. Olbrich, J. Organomet. Chem. 1999, 582, 58.
-
(1999)
J. Organomet. Chem.
, vol.582
, pp. 58
-
-
Neander, S.1
Tio, F.E.2
Buschmann, R.3
Behrens, U.4
Olbrich, F.5
|