-
1
-
-
80052022958
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-
For examples, see
-
For examples, see
-
-
-
-
4
-
-
34547182502
-
-
J. Wang, L.D. Heikkinen, H. Li, L. Zu, W. Jiang, H. Xie, and W. Wang Adv. Synth. Catal. 349 2007 1052 1056
-
(2007)
Adv. Synth. Catal.
, vol.349
, pp. 1052-1056
-
-
Wang, J.1
Heikkinen, L.D.2
Li, H.3
Zu, L.4
Jiang, W.5
Xie, H.6
Wang, W.7
-
9
-
-
57149139438
-
-
X. Chen, J. Wang, Y. Zhu, D. Shang, B. Gao, X. Liu, X. Feng, Z. Su, and C. Hu Chem. - Eur. J. 14 2008 10896 10899
-
(2008)
Chem. - Eur. J.
, vol.14
, pp. 10896-10899
-
-
Chen, X.1
Wang, J.2
Zhu, Y.3
Shang, D.4
Gao, B.5
Liu, X.6
Feng, X.7
Su, Z.8
Hu, C.9
-
13
-
-
44649125366
-
-
R. Kadyrov, J. Holz, B. Schaeffner, O. Zayas, J. Almena, and A. Boerner Tetrahedron: Asymmetry 19 2008 1189 1192
-
(2008)
Tetrahedron: Asymmetry
, vol.19
, pp. 1189-1192
-
-
Kadyrov, R.1
Holz, J.2
Schaeffner, B.3
Zayas, O.4
Almena, J.5
Boerner, A.6
-
14
-
-
67649647861
-
-
S. Doherty, J.G. Knight, A.L. Bell, S. El-Menabawey, C.M. Vogels, A. Decken, and S.A. Westcott Tetrahedron: Asymmetry 20 2009 1437 1444
-
(2009)
Tetrahedron: Asymmetry
, vol.20
, pp. 1437-1444
-
-
Doherty, S.1
Knight, J.G.2
Bell, A.L.3
El-Menabawey, S.4
Vogels, C.M.5
Decken, A.6
Westcott, S.A.7
-
15
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80052037151
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-
Ref. 1g. For examples of catalytic asymmetric synthesis of β-aminophosphonates and related compounds, see
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Ref. 1g. For examples of catalytic asymmetric synthesis of β-aminophosphonates and related compounds, see
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-
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16
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0032513064
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G. Cravotto, G.B. Giovenzana, R. Pagliarin, G. Palmisano, and M. Sisti Tetrahedron: Asymmetry 9 1998 745 748
-
(1998)
Tetrahedron: Asymmetry
, vol.9
, pp. 745-748
-
-
Cravotto, G.1
Giovenzana, G.B.2
Pagliarin, R.3
Palmisano, G.4
Sisti, M.5
-
19
-
-
80052028691
-
-
For reviews on β-aminophosphonic acids and their derivatives, see
-
For reviews on β-aminophosphonic acids and their derivatives, see
-
-
-
-
21
-
-
84891299621
-
-
E. Juaristi, V.A. Soloshonok, 2nd ed. Wiley Hoboken, New Jersey
-
F. Palacios, C. Alonso, and J.M. de Los Santos E. Juaristi, V.A. Soloshonok, Enantioselective Synthesis of β-Amino Acids 2nd ed. 2005 Wiley Hoboken, New Jersey 277 318
-
(2005)
Enantioselective Synthesis of β-Amino Acids
, pp. 277-318
-
-
Palacios, F.1
Alonso, C.2
De Los Santos, J.M.3
-
24
-
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80052032604
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For reviews on the phospha-Michael reaction, see
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For reviews on the phospha-Michael reaction, see
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-
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27
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79960466211
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S. Perera, V.K. Naganaboina, L. Wang, B. Zhang, Q. Guo, L. Rout, and C.-G. Zhao Adv. Synth. Catal. 353 2011 1729 1734
-
(2011)
Adv. Synth. Catal.
, vol.353
, pp. 1729-1734
-
-
Perera, S.1
Naganaboina, V.K.2
Wang, L.3
Zhang, B.4
Guo, Q.5
Rout, L.6
Zhao, C.-G.7
-
33
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79953213694
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During the preparation of this manuscript, Herrera and co-workers published their studies on this reaction catalyzed by some chiral thioureas in the presence of Hünig's base, including catalyst 4, but again poor ee value (9%) was obtained, see
-
During the preparation of this manuscript, Herrera and co-workers published their studies on this reaction catalyzed by some chiral thioureas in the presence of Hünig's base, including catalyst 4, but again poor ee value (9%) was obtained, see: A. Alcaine, E. Marqués-López, P. Merino, T. Tejero, and R.P. Herrera Org. Biomol. Chem. 9 2011 2777 2783
-
(2011)
Org. Biomol. Chem.
, vol.9
, pp. 2777-2783
-
-
Alcaine, A.1
Marqués-López, E.2
Merino, P.3
Tejero, T.4
Herrera, R.P.5
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36
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80052037595
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® resin cannot be absorbed by MS 4 , apparently the latter absorbs the acidic species generated from the resin under the reaction conditions.
-
® resin cannot be absorbed by MS 4, apparently the latter absorbs the acidic species generated from the resin under the reaction conditions.
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37
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80052036699
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31P absorption at 128.7 ppm, see
-
31P absorption at 128.7 ppm, see
-
-
-
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39
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0002604658
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The phosphonate form was reported to have a chemical shift of 0 ppm, see
-
The phosphonate form was reported to have a chemical shift of 0 ppm, see K. Moedritzer J. Inorg. Nucl. Chem. 22 1961 19 21
-
(1961)
J. Inorg. Nucl. Chem.
, vol.22
, pp. 19-21
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Moedritzer, K.1
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