-
1
-
-
0042238447
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-
See for example, T.J. Colacot Chem. Rev. 103 2003 3101 3118
-
(2003)
Chem. Rev.
, vol.103
, pp. 3101-3118
-
-
Colacot, T.J.1
-
5
-
-
79957766176
-
-
For ortho-lithiation of (N, N-dimethylamino)methyl ferrocene (Ugi's amine) see, for example
-
For ortho-lithiation of (N, N-dimethylamino)methyl ferrocene (Ugi's amine) see, for example
-
-
-
-
6
-
-
0343435902
-
-
D. Marquarding, H. Klusacek, G. Gokel, P. Hoffmann, and I. Ugi J. Am. Chem. Soc. 92 1970 5389 5393
-
(1970)
J. Am. Chem. Soc.
, vol.92
, pp. 5389-5393
-
-
Marquarding, D.1
Klusacek, H.2
Gokel, G.3
Hoffmann, P.4
Ugi, I.5
-
7
-
-
84981919807
-
-
D. Marquarding, H. Klusacek, G. Gokel, P. Hoffmann, and I. Ugi Angew. Chem. Int. Ed. Engl. 9 1970 371 372
-
(1970)
Angew. Chem. Int. Ed. Engl.
, vol.9
, pp. 371-372
-
-
Marquarding, D.1
Klusacek, H.2
Gokel, G.3
Hoffmann, P.4
Ugi, I.5
-
8
-
-
79957702977
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-
For ortho-lithiation of ferrocenes bearing an acetal substituent see, for example
-
For ortho-lithiation of ferrocenes bearing an acetal substituent see, for example
-
-
-
-
10
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-
0000715061
-
-
O. Riant, O. Samuel, T. Flessner, S. Taudien, and H.B.J. Kagan J. Org. Chem. 62 1997 6733 6745
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(1997)
J. Org. Chem.
, vol.62
, pp. 6733-6745
-
-
Riant, O.1
Samuel, O.2
Flessner, T.3
Taudien, S.4
Kagan, H.B.J.5
-
11
-
-
79957753028
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-
For ortho-lithiation of ferrocenes bearing a sulfinyl substituent see, for example
-
For ortho-lithiation of ferrocenes bearing a sulfinyl substituent see, for example
-
-
-
-
13
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0001059048
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-
O. Riant, G. Argouarch, D. Guillaneux, O. Samuel, and H.B. Kagan J. Org. Chem. 63 1998 3511 3514
-
(1998)
J. Org. Chem.
, vol.63
, pp. 3511-3514
-
-
Riant, O.1
Argouarch, G.2
Guillaneux, D.3
Samuel, O.4
Kagan, H.B.5
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14
-
-
31544467255
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-
To our knowledge the only spectroscopic report of a 1,2-derivatized ferrocene system featuring boron and phosphorus functionalities is that of a oxazaphospholidene oxide: D. Vinci, N. Mateus, X. Wu, F. Hancock, A. Steiner, and J. Xiao Org. Lett. 8 2006 215 218
-
(2006)
Org. Lett.
, vol.8
, pp. 215-218
-
-
Vinci, D.1
Mateus, N.2
Wu, X.3
Hancock, F.4
Steiner, A.5
Xiao, J.6
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16
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20644469225
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C. Bresner, S. Aldridge, I.A. Fallis, C. Jones, and L.-L. Ooi Angew. Chem. Int. Ed. 44 2005 3606 3609
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 3606-3609
-
-
Bresner, C.1
Aldridge, S.2
Fallis, I.A.3
Jones, C.4
Ooi, L.-L.5
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17
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33746436755
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-
C. Bresner, J.K. Day, N.D. Coombs, I.A. Fallis, S. Aldridge, S.J. Coles, and M.B. Hursthouse Dalton Trans. 2006 3660 3667
-
(2006)
Dalton Trans.
, pp. 3660-3667
-
-
Bresner, C.1
Day, J.K.2
Coombs, N.D.3
Fallis, I.A.4
Aldridge, S.5
Coles, S.J.6
Hursthouse, M.B.7
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18
-
-
34547690808
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J.K. Day, C. Bresner, I.A. Fallis, L.-L. Ooi, D.J. Watkin, S.J. Coles, L. Male, M.B. Hursthouse, and S. Aldridge Dalton Trans. 2007 3486 3488
-
(2007)
Dalton Trans.
, pp. 3486-3488
-
-
Day, J.K.1
Bresner, C.2
Fallis, I.A.3
Ooi, L.-L.4
Watkin, D.J.5
Coles, S.J.6
Male, L.7
Hursthouse, M.B.8
Aldridge, S.9
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19
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-
39749097879
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-
J.K. Day, C. Bresner, N.D. Coombs, I.A. Fallis, L.-L. Ooi, R.W. Harrington, W. Clegg, and S. Aldridge Inorg. Chem. 47 2008 793 804
-
(2008)
Inorg. Chem.
, vol.47
, pp. 793-804
-
-
Day, J.K.1
Bresner, C.2
Coombs, N.D.3
Fallis, I.A.4
Ooi, L.-L.5
Harrington, R.W.6
Clegg, W.7
Aldridge, S.8
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20
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53949109603
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-
A.E.J. Broomsgrove, D. Addy, C. Bresner, I.A. Fallis, A.L. Thompson, and S. Aldridge Chem. Eur. J. 14 2008 7525 7529
-
(2008)
Chem. Eur. J.
, vol.14
, pp. 7525-7529
-
-
Broomsgrove, A.E.J.1
Addy, D.2
Bresner, C.3
Fallis, I.A.4
Thompson, A.L.5
Aldridge, S.6
-
21
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72649104142
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-
I.R. Morgan, A. Di Paolo, D. Vidovic, I.A. Fallis, and S. Aldridge Chem. Commun. 2009 7288 7290
-
(2009)
Chem. Commun.
, pp. 7288-7290
-
-
Morgan, I.R.1
Di Paolo, A.2
Vidovic, D.3
Fallis, I.A.4
Aldridge, S.5
-
22
-
-
73349130043
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-
A.E.J. Broomsgrove, D. Addy, A. Di Paolo, I.R. Morgan, C. Bresner, V. Chislett, I.A. Fallis, A.L. Thompson, D. Vidovic, and S. Aldridge Inorg. Chem. 49 2010 157 173
-
(2010)
Inorg. Chem.
, vol.49
, pp. 157-173
-
-
Broomsgrove, A.E.J.1
Addy, D.2
Di Paolo, A.3
Morgan, I.R.4
Bresner, C.5
Chislett, V.6
Fallis, I.A.7
Thompson, A.L.8
Vidovic, D.9
Aldridge, S.10
-
23
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78149336675
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I.R. Morgan, A.E.J. Broomsgrove, P. Fitzpatrick, D. Vidovic, A.L. Thompson, I.A. Fallis, and S. Aldridge Organometallics 29 2010 4762 4765
-
(2010)
Organometallics
, vol.29
, pp. 4762-4765
-
-
Morgan, I.R.1
Broomsgrove, A.E.J.2
Fitzpatrick, P.3
Vidovic, D.4
Thompson, A.L.5
Fallis, I.A.6
Aldridge, S.7
-
24
-
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77955063465
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C. Bresner, D.A. Haynes Addy, A.E.J. Broomsgrove, P. Fitzpatrick, D. Vidovic, A.L. Thompson, I.A. Fallis, and S. Aldridge New J. Chem. 34 2010 1652 1659
-
(2010)
New J. Chem.
, vol.34
, pp. 1652-1659
-
-
Bresner, C.1
Haynes Addy, D.A.2
Broomsgrove, A.E.J.3
Fitzpatrick, P.4
Vidovic, D.5
Thompson, A.L.6
Fallis, I.A.7
Aldridge, S.8
-
26
-
-
79957675590
-
-
The Schlögel nomenclature is used to describe the planar chirality at the 1,2-disubstituted ferrocenes
-
The Schlögel nomenclature is used to describe the planar chirality at the 1,2-disubstituted ferrocenes
-
-
-
-
29
-
-
79957784068
-
-
Further examples
-
Further examples
-
-
-
-
32
-
-
79957768917
-
-
Note
-
3 of Mes), boron-bound quaternary carbons not observed. 11B (96 MHz, [D]chloroform, 20 °C, ppm): δB = 74.
-
-
-
-
37
-
-
79957678040
-
-
The enantiomeric excess of the product could not be determined due to its very low polarity
-
The enantiomeric excess of the product could not be determined due to its very low polarity.
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-
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