-
1
-
-
11844273232
-
-
Coumbarides G.S., Eames J., Flinn A., Northen J., and Yohannes Y. Tetrahedron Lett. 46 (2005) 849-853
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 849-853
-
-
Coumbarides, G.S.1
Eames, J.2
Flinn, A.3
Northen, J.4
Yohannes, Y.5
-
2
-
-
33846664160
-
-
Chavda S., Coulbeck E., Coumbarides G.S., Dingjan M., Eames J., Ghilagaber S., and Yohannes Y. Tetrahedron: Asymmetry 17 (2006) 3386-3399
-
(2006)
Tetrahedron: Asymmetry
, vol.17
, pp. 3386-3399
-
-
Chavda, S.1
Coulbeck, E.2
Coumbarides, G.S.3
Dingjan, M.4
Eames, J.5
Ghilagaber, S.6
Yohannes, Y.7
-
3
-
-
33846806105
-
-
Boyd E., Chavda S., Coulbeck E., Coumbarides G.S., Dingjan M., Eames J., Flinn A., Krishnamurthy A.K., Namutebi M., Northen J., and Yohannes Y. Tetrahedron: Asymmetry 17 (2006) 3406-3422
-
(2006)
Tetrahedron: Asymmetry
, vol.17
, pp. 3406-3422
-
-
Boyd, E.1
Chavda, S.2
Coulbeck, E.3
Coumbarides, G.S.4
Dingjan, M.5
Eames, J.6
Flinn, A.7
Krishnamurthy, A.K.8
Namutebi, M.9
Northen, J.10
Yohannes, Y.11
-
5
-
-
34247492713
-
-
Coumbarides G.S., Dingjan M., Eames J., Flinn A., and Northen J. Chirality 19 (2007) 321-328
-
(2007)
Chirality
, vol.19
, pp. 321-328
-
-
Coumbarides, G.S.1
Dingjan, M.2
Eames, J.3
Flinn, A.4
Northen, J.5
-
6
-
-
34247497606
-
-
Chavda S., Coumbarides G.S., Dingjan M., Eames J., Flinn A., and Northen J. Chirality 19 (2007) 313-320
-
(2007)
Chirality
, vol.19
, pp. 313-320
-
-
Chavda, S.1
Coumbarides, G.S.2
Dingjan, M.3
Eames, J.4
Flinn, A.5
Northen, J.6
-
7
-
-
15944408858
-
-
Coumbarides G.S., Dingjan M., Eames J., Flinn A., Northen J., and Yohannes Y. Tetrahedron Lett. 46 (2005) 2897-2902
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 2897-2902
-
-
Coumbarides, G.S.1
Dingjan, M.2
Eames, J.3
Flinn, A.4
Northen, J.5
Yohannes, Y.6
-
8
-
-
30544437360
-
-
Coumbarides G.S., Dingjan M., Eames J., Flinn A., Motevalli M., Northen J., and Yohannes Y. Synlett (2006) 101-105
-
(2006)
Synlett
, pp. 101-105
-
-
Coumbarides, G.S.1
Dingjan, M.2
Eames, J.3
Flinn, A.4
Motevalli, M.5
Northen, J.6
Yohannes, Y.7
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9
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43849104668
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note
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Using 2 equiv of 4-isopropyl-oxazolidin-2-one rac-2 gave the corresponding oxazolidin-2-ones (S,R)-syn- and (S,S)-anti-10 (ratio: 81:19) with reduced diastereoselection.
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10
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43849094225
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note
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Determined by the splitting (∼1.6 Hz) at 4.06 ppm {measured at 400 MHz using a chiral shift NMR reagent, tris[3-(trifluoromethylhydroxymethylene)-d-camphorato] europium (III)}.
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12
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0000184426
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For additional reports into the use of 4-isopropyl-oxazolidin-2-one, see:
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For additional reports into the use of 4-isopropyl-oxazolidin-2-one, see:. Doyle M.P., Dorow R.L., Terpstra J.W., and Rodenhouse R.A. J. Org. Chem. 50 (1985) 1663-1666
-
(1985)
J. Org. Chem.
, vol.50
, pp. 1663-1666
-
-
Doyle, M.P.1
Dorow, R.L.2
Terpstra, J.W.3
Rodenhouse, R.A.4
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14
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0025006864
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Evans D.A., Dow R.L., Shih T.L., Takacs J.M., and Zahler R. J. Am. Chem. Soc. 112 (1990) 5290-5313
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 5290-5313
-
-
Evans, D.A.1
Dow, R.L.2
Shih, T.L.3
Takacs, J.M.4
Zahler, R.5
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21
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0034725737
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-
Casadei M.A., Feroci M., Inesi A., Rossi L., and Sotgiu G. J. Org. Chem. 65 (2000) 4759-4761
-
(2000)
J. Org. Chem.
, vol.65
, pp. 4759-4761
-
-
Casadei, M.A.1
Feroci, M.2
Inesi, A.3
Rossi, L.4
Sotgiu, G.5
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23
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0034824178
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-
Palomo C., Oiarbide M., Dias F., Ortiz A., and Linden A. J. Am. Chem. Soc. 123 (2001) 5602-5603
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 5602-5603
-
-
Palomo, C.1
Oiarbide, M.2
Dias, F.3
Ortiz, A.4
Linden, A.5
-
24
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0037068116
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Feroci M., Gennaro A., Inesi A., Orsini M., and Palombi L. Tetrahedron Lett. 43 (2002) 5863-5865
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 5863-5865
-
-
Feroci, M.1
Gennaro, A.2
Inesi, A.3
Orsini, M.4
Palombi, L.5
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32
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43849086515
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Lancaster Chemical catalogue, 2002-2003, p 1106; the name contradicts the sign of rotation for both compounds.
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Lancaster Chemical catalogue, 2002-2003, p 1106; the name contradicts the sign of rotation for both compounds.
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35
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0033978397
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Suzuki M., Yamazaki T., Ohta H., Shima K., Ohi K., Nishiyama S., and Sugai T. Synlett (2000) 189-192
-
(2000)
Synlett
, pp. 189-192
-
-
Suzuki, M.1
Yamazaki, T.2
Ohta, H.3
Shima, K.4
Ohi, K.5
Nishiyama, S.6
Sugai, T.7
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36
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43849106984
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Chiral compounds and reference catalogue, Oxford Asymmetry, 1997, p 34.
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Chiral compounds and reference catalogue, Oxford Asymmetry, 1997, p 34.
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37
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43849104361
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Sigma Aldrich Limited, Chemical catalogue, 2005-2006, p 1472.
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Sigma Aldrich Limited, Chemical catalogue, 2005-2006, p 1472.
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41
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33748621482
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Burns B., King N.P., Tye H., Studley J.R., Gamble M., and Wills M. J. Chem. Soc., Perkin Trans. 1 (1998) 1027-1038
-
(1998)
J. Chem. Soc., Perkin Trans. 1
, pp. 1027-1038
-
-
Burns, B.1
King, N.P.2
Tye, H.3
Studley, J.R.4
Gamble, M.5
Wills, M.6
-
44
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33644922428
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-
Alouane N., Boutier A., Baron C., Vrancken E., and Mangeney P. Synthesis (2006) 885-889
-
(2006)
Synthesis
, pp. 885-889
-
-
Alouane, N.1
Boutier, A.2
Baron, C.3
Vrancken, E.4
Mangeney, P.5
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46
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43849112532
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ACROS, Chemical catalogue, 2006-2007, p 1133; both enantiomers of oxazolidin-2-one 2 have the same sign and specific rotation.
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ACROS, Chemical catalogue, 2006-2007, p 1133; both enantiomers of oxazolidin-2-one 2 have the same sign and specific rotation.
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48
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43849096619
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note
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4.
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49
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43849099724
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note
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26 = + 107.3 (c 3.4, EtOH)} no change of sign occurred.
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55
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34548313823
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Mukhopadhyay P., Zuber G., Wipf P., and Beratan D.N. Angew. Chem., Int. Ed. 46 (2007) 6450-6452
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 6450-6452
-
-
Mukhopadhyay, P.1
Zuber, G.2
Wipf, P.3
Beratan, D.N.4
-
63
-
-
34548823484
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-
Rossi S., Le Nostro P., Lagi M., Ninham B.W., and Baglioni P. J. Phys. Chem. B 111 (2007) 10510-10519
-
(2007)
J. Phys. Chem. B
, vol.111
, pp. 10510-10519
-
-
Rossi, S.1
Le Nostro, P.2
Lagi, M.3
Ninham, B.W.4
Baglioni, P.5
-
66
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43849086342
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-
Enraf-Nonius CAD-4/PC Software: Version 1.5c; Enraf-Nonius: Delft, The Netherlands, 1994.
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Enraf-Nonius CAD-4/PC Software: Version 1.5c; Enraf-Nonius: Delft, The Netherlands, 1994.
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-
68
-
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43849098625
-
-
Harms, K.; Wocadlo, S. xcad4-CAD4 Data Reduction; University of Marburg: Marburg, Germany, 1995.
-
Harms, K.; Wocadlo, S. xcad4-CAD4 Data Reduction; University of Marburg: Marburg, Germany, 1995.
-
-
-
-
72
-
-
43849097264
-
-
CPMD, Copyright IBM Corp 1990-2004, Copyright MPI für Festkörperforschung Stuttgart, 1997-2001.
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CPMD, Copyright IBM Corp 1990-2004, Copyright MPI für Festkörperforschung Stuttgart, 1997-2001.
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