-
2
-
-
0033935279
-
-
Representative examples: a conjugated addition of alkylzinc reagents to ketones: B. L. Feringa, Acc. Chem. Res. 2000, 33, 346-353;
-
Representative examples: a) conjugated addition of alkylzinc reagents to ketones: B. L. Feringa, Acc. Chem. Res. 2000, 33, 346-353;
-
-
-
-
3
-
-
13244251142
-
-
Rh-catalysed asymmetric hydrogenation: H. Bernsman, M. van der Berg, R. Hoen, A. J. Minnaard, G. Mehler, M. T. Reetz, J. G. de Vries, B. L. Feringa, J. Org. Chem. 2005, 70, 943-951;
-
b) Rh-catalysed asymmetric hydrogenation: H. Bernsman, M. van der Berg, R. Hoen, A. J. Minnaard, G. Mehler, M. T. Reetz, J. G. de Vries, B. L. Feringa, J. Org. Chem. 2005, 70, 943-951;
-
-
-
-
4
-
-
0037028545
-
-
c) Nicatalysed hydrovinylation: G. Francio, F. Faraone, W. Leitner, J. Am. Chem. Soc. 2002, 124, 736-737;
-
(2002)
J. Am. Chem. Soc
, vol.124
, pp. 736-737
-
-
Nicatalysed hydrovinylation, G.1
Francio, F.2
Faraone, W.L.3
-
5
-
-
27644546852
-
-
Ir-catalysed allylic animation: A Leitner, S. Shekhar, M. J. Pouy, J. F. Hartwig, J. Am. Chem. Soc. 2005, 127, 15506-15514;
-
d) Ir-catalysed allylic animation: A Leitner, S. Shekhar, M. J. Pouy, J. F. Hartwig, J. Am. Chem. Soc. 2005, 127, 15506-15514;
-
-
-
-
6
-
-
33344469112
-
-
Rh-catalysed arylation of aldehydes: R. B. C. Jagt, P. Y. Toullec, J. G. de Vries, B. L. Feringa, A. J. Minnaard, Org. Biomol. Chem. 2006, 4, 773-775.
-
e) Rh-catalysed arylation of aldehydes: R. B. C. Jagt, P. Y. Toullec, J. G. de Vries, B. L. Feringa, A. J. Minnaard, Org. Biomol. Chem. 2006, 4, 773-775.
-
-
-
-
11
-
-
33947092416
-
-
a) D. J. Cram, R. C. Helgeson, S. C. Peacock, L. J. Kaplan, L. A. Domeier, P. Moreau, K. Koga, J. M. Mayer, Y. Chao, M. G. Siegel, D.H. Hoffman, G.D. Sogah, J. Org. Chem. 1978, 43, 1930-1946;
-
(1978)
J. Org. Chem
, vol.43
, pp. 1930-1946
-
-
Cram, D.J.1
Helgeson, R.C.2
Peacock, S.C.3
Kaplan, L.J.4
Domeier, L.A.5
Moreau, P.6
Koga, K.7
Mayer, J.M.8
Chao, Y.9
Siegel, M.G.10
Hoffman, D.H.11
Sogah, G.D.12
-
13
-
-
0026518693
-
-
c) P. J. Cox, W. Wang, V. Snieckus, Tetrahedron Lett. 1992, 33, 2253-2256;
-
(1992)
Tetrahedron Lett
, vol.33
, pp. 2253-2256
-
-
Cox, P.J.1
Wang, W.2
Snieckus, V.3
-
14
-
-
0034725134
-
-
d) L. A. Arnold, R. Imbos, A. Mandoli, A. H. M. de Vries, R. Naasz, B. L. Feringa, Tetrahedron 2000, 56, 2865-2878.
-
(2000)
Tetrahedron
, vol.56
, pp. 2865-2878
-
-
Arnold, L.A.1
Imbos, R.2
Mandoli, A.3
de Vries, A.H.M.4
Naasz, R.5
Feringa, B.L.6
-
15
-
-
34247139301
-
-
R. Kargbo, Y. Takahashi, S. Bhor, G. R. Cook, G. C. Lloyd-Jones, I. R. Shepperson, J. Am. Chem. Soc. 2007, 129, 3846-3847.
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 3846-3847
-
-
Kargbo, R.1
Takahashi, Y.2
Bhor, S.3
Cook, G.R.4
Lloyd-Jones, G.C.5
Shepperson, I.R.6
-
17
-
-
33745813188
-
-
b) Z. Zhao, J. Messinger, U. Schön, R. Wartchow, H. Butenschön, Chem. Commun. 2006, 3007-3009;
-
(2006)
Chem. Commun
, pp. 3007-3009
-
-
Zhao, Z.1
Messinger, J.2
Schön, U.3
Wartchow, R.4
Butenschön, H.5
-
18
-
-
53849144921
-
-
c) A. M. Dyke, D. M. Gill, J. N. Harvey, A. J. Hester, G. C. Lloyd-Jones, M. P. Muñoz, I. R. Shepperson, Angew. Chem. 2008, 120, 5145;
-
(2008)
Angew. Chem
, vol.120
, pp. 5145
-
-
Dyke, A.M.1
Gill, D.M.2
Harvey, J.N.3
Hester, A.J.4
Lloyd-Jones, G.C.5
Muñoz, M.P.6
Shepperson, I.R.7
-
19
-
-
49849097111
-
-
Angew. Chem. Int. Ed. 2008, 47, 5067-5070.
-
(2008)
Angew. Chem. Int. Ed
, vol.47
, pp. 5067-5070
-
-
-
20
-
-
53849142082
-
-
3→R). have proven of utility in asymmetric hydrogenation (M. P. Muñoz, I. R. Shepperson, G. C. Lloyd-Jones, W. Leitner, G. Franco, unpublished results).
-
3→R). have proven of utility in asymmetric hydrogenation (M. P. Muñoz, I. R. Shepperson, G. C. Lloyd-Jones, W. Leitner, G. Franco, unpublished results).
-
-
-
-
21
-
-
22544438755
-
-
a) M. T. Reetz, J.-A. Ma, R. Goddard, Angew. Chem. 2005, 117, 416-419;
-
(2005)
Angew. Chem
, vol.117
, pp. 416-419
-
-
Reetz, M.T.1
Ma, J.-A.2
Goddard, R.3
-
22
-
-
12344268139
-
-
Angew. Chem. Int. Ed. 2005, 44, 412-415;
-
(2005)
Angew. Chem. Int. Ed
, vol.44
, pp. 412-415
-
-
-
24
-
-
18844381406
-
-
Angew. Chem. Int. Ed. 2005, 44, 2959-2962.
-
(2005)
Angew. Chem. Int. Ed
, vol.44
, pp. 2959-2962
-
-
-
25
-
-
53849086061
-
-
3→R). will be reported in full in due course: M. Kruck, M. P. Munoz, C. P. Butts, G. C. Lloyd-Jones, unpublished results.
-
3→R). will be reported in full in due course: M. Kruck, M. P. Munoz, C. P. Butts, G. C. Lloyd-Jones, unpublished results.
-
-
-
-
26
-
-
53849119778
-
-
Reetz has reported (reference [8, that in species analogous to 3. where CH2O2CPh or SiPh3 replaces SO 2:CF3, the 31P NMR chemical shift order for the diastereomers (assigned by X-ray crystallography) is consistent (δP S,SP > δP S,RP, This relationship was then employed by Reetz to assign diastereoisomeric identity to a range of other analogues. Whilst the SO 2CF3 group has rather unique properties,[5,6] the correlation does indeed hold for 3 δP 3SS= 155.50; δP 3= 151.31
-
P 3= 151.31).
-
-
-
-
28
-
-
0000977865
-
-
For a summary, see:, Eds, D.M. Grant, R. K. Harris, Wiley, Chichester
-
For a summary, see: F. B. Mallory. C. W. Mallory, in Encyclopedia of Nuclear Magnetic Resonance (Eds.: D.M. Grant, R. K. Harris), Wiley, Chichester, 1996, pp. 1491.
-
(1996)
Encyclopedia of Nuclear Magnetic Resonance
, pp. 1491
-
-
Mallory, F.B.1
Mallory, C.W.2
-
31
-
-
50549160772
-
-
G. Allen, G. Gee, G. J. Wilson, Polymer 1960, 1, 456-466.
-
(1960)
Polymer
, vol.1
, pp. 456-466
-
-
Allen, G.1
Gee, G.2
Wilson, G.J.3
-
32
-
-
0001682618
-
-
G. R. Miller, A. W. Yankowsky, S. O. Grim, J. Chem. Phys. 1969, 51, 3185-3190.
-
(1969)
J. Chem. Phys
, vol.51
, pp. 3185-3190
-
-
Miller, G.R.1
Yankowsky, A.W.2
Grim, S.O.3
-
33
-
-
4544291407
-
-
V. N. Kartsev, M. N. Rodnikova, S. N. Shtykov, J. Struct. Chem. 2004, 45, 91-95.
-
(2004)
J. Struct. Chem
, vol.45
, pp. 91-95
-
-
Kartsev, V.N.1
Rodnikova, M.N.2
Shtykov, S.N.3
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