-
8
-
-
40849138216
-
-
See, inter alia:
-
See, inter alia:
-
-
-
-
9
-
-
0343435902
-
-
Marquarding D., Klusacek H., Gokel G., Hoffmann P., and Ugi I. J. Am. Chem. Soc. 92 (1970) 5389
-
(1970)
J. Am. Chem. Soc.
, vol.92
, pp. 5389
-
-
Marquarding, D.1
Klusacek, H.2
Gokel, G.3
Hoffmann, P.4
Ugi, I.5
-
17
-
-
0033840155
-
-
Fukuzawa S., Tsuchiya D., Sasamoto K., Hirano K., and Ohtaguchi M. Eur. J. Org. Chem. (2000) 2877
-
(2000)
Eur. J. Org. Chem.
, pp. 2877
-
-
Fukuzawa, S.1
Tsuchiya, D.2
Sasamoto, K.3
Hirano, K.4
Ohtaguchi, M.5
-
21
-
-
40849150917
-
-
For other additions to aldehyde 5, see:
-
For other additions to aldehyde 5, see:
-
-
-
-
22
-
-
40849096459
-
-
Gokel G., Hoffmann P., Kleimann H., Klusacek H., Marquarding D., and Ugi I. Tetrahedron Lett. (1970) 1771
-
(1970)
Tetrahedron Lett.
, pp. 1771
-
-
Gokel, G.1
Hoffmann, P.2
Kleimann, H.3
Klusacek, H.4
Marquarding, D.5
Ugi, I.6
-
24
-
-
40849141281
-
-
Reviews:
-
Reviews:
-
-
-
-
29
-
-
34447580092
-
-
Plasson R., Kondepudi D.K., Bersini H., Commeyras A., and Asakura K. Chirality 19 (2007) 589
-
(2007)
Chirality
, vol.19
, pp. 589
-
-
Plasson, R.1
Kondepudi, D.K.2
Bersini, H.3
Commeyras, A.4
Asakura, K.5
-
31
-
-
40849115146
-
-
For related reactions, see:
-
For related reactions, see:
-
-
-
-
34
-
-
0037031630
-
-
Readily obtained from 2-chloropyrimidine as described in:
-
Readily obtained from 2-chloropyrimidine as described in:. Vlád G., and Horváth I.T. J. Org. Chem. 67 (2002) 6550
-
(2002)
J. Org. Chem.
, vol.67
, pp. 6550
-
-
Vlád, G.1
Horváth, I.T.2
-
36
-
-
0000715061
-
-
Riant O., Samuel O., Flessner T., Taudien S., and Kagan H.B. J. Org. Chem. 62 (1997) 6733
-
(1997)
J. Org. Chem.
, vol.62
, pp. 6733
-
-
Riant, O.1
Samuel, O.2
Flessner, T.3
Taudien, S.4
Kagan, H.B.5
-
37
-
-
40849089435
-
-
note
-
2=0.1265. Crystallographic data (excluding structure factors) for this structure have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no CCDC-663416. Copies of the data can be obtained, free of charge, on application to The Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK, (fax: +44 (0)1223 336033 or e-mail: deposit@ccdc.cam.ac.uk).
-
-
-
-
38
-
-
40849120242
-
-
note
-
13
-
-
-
-
40
-
-
0000914701
-
-
Solà L., Reddy K.S., Vidal-Ferran A., Moyano A., Pericàs M.A., Riera A., Álvarez-Larena A., and Piniella J.-F. J. Org. Chem. 63 (1998) 7078
-
(1998)
J. Org. Chem.
, vol.63
, pp. 7078
-
-
Solà, L.1
Reddy, K.S.2
Vidal-Ferran, A.3
Moyano, A.4
Pericàs, M.A.5
Riera, A.6
Álvarez-Larena, A.7
Piniella, J.-F.8
-
41
-
-
0033612195
-
-
Solà L., Reddy K.S., Vidal-Ferran A., Moyano A., Pericàs M.A., and Riera A. J. Org. Chem. 64 (1999) 3969
-
(1999)
J. Org. Chem.
, vol.64
, pp. 3969
-
-
Solà, L.1
Reddy, K.S.2
Vidal-Ferran, A.3
Moyano, A.4
Pericàs, M.A.5
Riera, A.6
-
43
-
-
24144495215
-
-
García-Delgado N., Reddy K.S., Solà L., Riera A., Pericàs M.A., and Verdaguer X. J. Org. Chem. 70 (2005) 7426
-
(2005)
J. Org. Chem.
, vol.70
, pp. 7426
-
-
García-Delgado, N.1
Reddy, K.S.2
Solà, L.3
Riera, A.4
Pericàs, M.A.5
Verdaguer, X.6
-
45
-
-
1942532912
-
-
Rapid intramolecular alkyl transfer in a chelated intermediate has been previously proposed for the fast, highly diastereoselective addition of dialkylzinc reagents to atropisomeric 2-formyl arylamides:
-
Rapid intramolecular alkyl transfer in a chelated intermediate has been previously proposed for the fast, highly diastereoselective addition of dialkylzinc reagents to atropisomeric 2-formyl arylamides:. Jimeno C., Rios R., Carroll P.J., and Walsh P.J. Tetrahedron 60 (2004) 4543
-
(2004)
Tetrahedron
, vol.60
, pp. 4543
-
-
Jimeno, C.1
Rios, R.2
Carroll, P.J.3
Walsh, P.J.4
-
46
-
-
40849120241
-
-
note
-
-1, respectively).
-
-
-
-
47
-
-
40849139746
-
-
note
-
® package of programs.
-
-
-
-
48
-
-
40849106910
-
-
note
-
18 suitable for the intramolecular transfer of an alkyl group.
-
-
-
-
50
-
-
40849088397
-
-
For the application of structurally related (2-substituted) ferrocenylcarbinols as chiral ligands in asymmetric catalysis, see inter alia:
-
For the application of structurally related (2-substituted) ferrocenylcarbinols as chiral ligands in asymmetric catalysis, see inter alia:
-
-
-
-
55
-
-
32544441556
-
-
Wölfle H., Kopacka H., Wurst K., Ongania K., Görtz H., Preishuber-Pflügl P., and Bildstein B. J. Organomet. Chem. 691 (2006) 1197
-
(2006)
J. Organomet. Chem.
, vol.691
, pp. 1197
-
-
Wölfle, H.1
Kopacka, H.2
Wurst, K.3
Ongania, K.4
Görtz, H.5
Preishuber-Pflügl, P.6
Bildstein, B.7
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