-
1
-
-
1942456786
-
-
Wijtmans, R.; Vink, M. K. S.; Schoemaker, H. E.; Van Delft, F. L.; Blaauw, R. H.; Rutjes, F. P. J. T. Synthesis 2004, 641-662
-
(2004)
Synthesis
, pp. 641-662
-
-
Wijtmans, R.1
Vink, M.K.S.2
Schoemaker, H.E.3
Van Delft, F.L.4
Blaauw, R.H.5
Rutjes, F.P.J.T.6
-
3
-
-
33344455013
-
-
Forsyth, S. A.; Gunaratne, H. Q. N.; Hardacre, C.; McKeown, A.; Rooney, D. W. Org. Process Res. Dev. 2006, 10, 94-102
-
(2006)
Org. Process Res. Dev.
, vol.10
, pp. 94-102
-
-
Forsyth, S.A.1
Gunaratne, H.Q.N.2
Hardacre, C.3
McKeown, A.4
Rooney, D.W.5
-
4
-
-
33751385275
-
-
Uozumi, Y.; Tanahashi, A.; Hayashi, T. J. Org. Chem. 1993, 58, 6826-6832
-
(1993)
J. Org. Chem.
, vol.58
, pp. 6826-6832
-
-
Uozumi, Y.1
Tanahashi, A.2
Hayashi, T.3
-
6
-
-
4444229491
-
-
Ito, K.; Imahayashi, Y.; Kuroda, T.; Eno, S.; Saito, B.; Katsuki, T. Tetrahedron Lett. 2004, 45, 7277-7281
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 7277-7281
-
-
Ito, K.1
Imahayashi, Y.2
Kuroda, T.3
Eno, S.4
Saito, B.5
Katsuki, T.6
-
7
-
-
0034622923
-
-
Massacret, M.; Lakhmiri, R.; Lhoste, P.; Nguefack, C.; Ben Abdelouahab, F. B.; Fadel, R.; Sinou, D. Tetrahedron: Asymmetry 2000, 11, 3561-3568
-
(2000)
Tetrahedron: Asymmetry
, vol.11
, pp. 3561-3568
-
-
Massacret, M.1
Lakhmiri, R.2
Lhoste, P.3
Nguefack, C.4
Ben Abdelouahab, F.B.5
Fadel, R.6
Sinou, D.7
-
9
-
-
0037152333
-
-
Nakano, H.; Yokoyama, J.-i.; Fujita, R.; Hongo, H. Tetrahedron Lett. 2002, 43, 7761-7764
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 7761-7764
-
-
Nakano, H.1
Y, J.-I.2
Fujita, R.3
Hongo, H.4
-
10
-
-
0028203787
-
-
Enders, D.; Meyer, O.; Raabe, G.; Runsink, J. Synthesis 1994, 66-72
-
(1994)
Synthesis
, pp. 66-72
-
-
Enders, D.1
Meyer, O.2
Raabe, G.3
Runsink, J.4
-
11
-
-
0000780856
-
-
Baldoli, C.; Del Buttero, P.; Licandro, E.; Maiorana, S.; Papagni, A.; Zanotti Gerosa, A. J. Organomet. Chem. 1995, 486, 279-282
-
(1995)
J. Organomet. Chem.
, vol.486
, pp. 279-282
-
-
Baldoli, C.1
Del Buttero, P.2
Licandro, E.3
Maiorana, S.4
Papagni, A.5
Zanotti Gerosa, A.6
-
12
-
-
0002816836
-
-
Licandro, E.; Maiorana, S.; Capella, L.; Manzotti, R.; Papagni, A.; Pryce, M.; Graiff, C.; Tiripicchio, A. Eur. J. Org. Chem. 1998, 212, 7-2133
-
(1998)
Eur. J. Org. Chem.
, vol.212
, pp. 7-2133
-
-
Licandro, E.1
Maiorana, S.2
Capella, L.3
Manzotti, R.4
Papagni, A.5
Pryce, M.6
Graiff, C.7
Tiripicchio, A.8
-
14
-
-
0033214938
-
-
Bouron, E.; Goussard, G.; Marchand, C.; Bonin, M.; Pannecoucke, X.; Quirion, J.-C.; Husson, H.-P. Tetrahedron Lett. 1999, 40, 7227-7230
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 7227-7230
-
-
Bouron, E.1
Goussard, G.2
Marchand, C.3
Bonin, M.4
Pannecoucke, X.5
Quirion, J.-C.6
Husson, H.-P.7
-
15
-
-
8444232793
-
-
Lupi, V.; Albanese, D.; Landini, D.; Scaletti, D.; Penso, M. Tetrahedron 2004, 60, 11709-11718
-
(2004)
Tetrahedron
, vol.60
, pp. 11709-11718
-
-
Lupi, V.1
Albanese, D.2
Landini, D.3
Scaletti, D.4
Penso, M.5
-
16
-
-
34250648937
-
-
Albanese, D.; Salsa, M.; Landini, D.; Lupi, V.; Penso, M. Eur. J. Org. Chem. 2007, 210, 7-2113
-
(2007)
Eur. J. Org. Chem.
, vol.210
, pp. 7-2113
-
-
Albanese, D.1
Salsa, M.2
Landini, D.3
Lupi, V.4
Penso, M.5
-
17
-
-
54349121133
-
-
Penso, M.; Lupi, V.; Albanese, D.; Foschi, F.; Landini, D.; Tagliabue, A. Synlett 2008, 2451-2454
-
(2008)
Synlett
, pp. 2451-2454
-
-
Penso, M.1
Lupi, V.2
Albanese, D.3
Foschi, F.4
Landini, D.5
Tagliabue, A.6
-
18
-
-
57849165735
-
-
Albanese, D.; Foschi, F.; Penso, M. Catal. Today 2009, 140, 100-104
-
(2009)
Catal. Today
, vol.140
, pp. 100-104
-
-
Albanese, D.1
Foschi, F.2
Penso, M.3
-
20
-
-
37549039127
-
-
Hodgson, D. M.; Humphreys, P. G.; Miles, S. M.; Brierley, C. A. J.; Ward, J. G. J. Org. Chem. 2007, 72, 10009-10021
-
(2007)
J. Org. Chem.
, vol.72
, pp. 10009-10021
-
-
Hodgson, D.M.1
Humphreys, P.G.2
Miles, S.M.3
Brierley, C.A.J.4
Ward, J.G.5
-
21
-
-
77952922480
-
-
1H NMR of 11a proved to be identical to that previously published (ref 7)
-
1H NMR of 11a proved to be identical to that previously published (ref 7).
-
-
-
-
22
-
-
77952902509
-
-
Morpholines have been shown to be enantiomerically pure by HPLC on chiral column. Racemic morpholines have been prepared as analytical standards from the ring opening of racemic epoxides
-
Morpholines have been shown to be enantiomerically pure by HPLC on chiral column. Racemic morpholines have been prepared as analytical standards from the ring opening of racemic epoxides.
-
-
-
-
23
-
-
77952931961
-
-
Retention times for the racemic mixture: 20.6, 24.2, 28.8, 30.8 min
-
Retention times for the racemic mixture: 20.6, 24.2, 28.8, 30.8 min.
-
-
-
-
24
-
-
77952927178
-
-
Retention times for the racemic mixture: 18.6, 20.2, 22.5, 25.2 min
-
Retention times for the racemic mixture: 18.6, 20.2, 22.5, 25.2 min.
-
-
-
|