-
1
-
-
84863608219
-
-
Patent WO2007/93021 A1
-
Moreira de Almeida, I. Patent WO2007/93021 A1, 2007.
-
(2007)
-
-
Moreira De Almeida, I.1
-
2
-
-
84863626267
-
-
Patent EP1876179 A1
-
Murata, T.; Makino, S. Patent EP1876179 A1, 2008.
-
(2008)
-
-
Murata, T.1
Makino, S.2
-
3
-
-
84863626268
-
-
Patent WO2008/133884 A2
-
Jin, X.; Staunton, J.; MacDonald, D.; Dong, H.; Kifle, L. Patent WO2008/133884 A2, 2008.
-
(2008)
-
-
Jin, X.1
Staunton, J.2
MacDonald, D.3
Dong, H.4
Kifle, L.5
-
4
-
-
77956617367
-
-
Soares, A. M. S.; Costa, S. P. G.; Gonalves, M; Sameiro, T. Tetrahedron 2010, 66, 8189
-
(2010)
Tetrahedron
, vol.66
, pp. 8189
-
-
Soares, A.M.S.1
Costa, S.P.G.2
Gonalves, M.3
Sameiro, T.4
-
5
-
-
79953217992
-
-
Sheng, C.; Che, X.; Wang, W.; Wang, S.; Cao, Y.; Yao, Y.; Miao, Z.; Zhang, W. Eur. J. Med. Chem. 2011, 46, 1706
-
(2011)
Eur. J. Med. Chem.
, vol.46
, pp. 1706
-
-
Sheng, C.1
Che, X.2
Wang, W.3
Wang, S.4
Cao, Y.5
Yao, Y.6
Miao, Z.7
Zhang, W.8
-
6
-
-
84863625788
-
-
Patent US2004/14977 A1
-
Fukuda, S.; Nakamura, A.; Shimizu, M.; Okada, T.; Oohida, S.; Asahara, T. Patent US2004/14977 A1, 2004.
-
(2004)
-
-
Fukuda, S.1
Nakamura, A.2
Shimizu, M.3
Okada, T.4
Oohida, S.5
Asahara, T.6
-
7
-
-
78649636396
-
-
Khaksar, S.; Heydari, A.; Tajbakhsh, M.; Vahdat, S. M. J. Fluorine Chem. 2010, 131, 1377
-
(2010)
J. Fluorine Chem.
, vol.131
, pp. 1377
-
-
Khaksar, S.1
Heydari, A.2
Tajbakhsh, M.3
Vahdat, S.M.4
-
8
-
-
33846026688
-
-
Zhang, Z. H.; Li, T. S.; Li, J. J. Monatsh. Chem. 2007, 138, 89
-
(2007)
Monatsh. Chem.
, vol.138
, pp. 89
-
-
Zhang, Z.H.1
Li, T.S.2
Li, J.J.3
-
10
-
-
84863626695
-
-
Heravi, M. M.; Montazeri, N.; Rahmizadeh, M.; Bakavoli, M.; Ghassemzadehb, M. J. Chem. Res. 2000, 12, 284
-
(2000)
J. Chem. Res.
, vol.12
, pp. 284
-
-
Heravi, M.M.1
Montazeri, N.2
Rahmizadeh, M.3
Bakavoli, M.4
Ghassemzadehb, M.5
-
11
-
-
34248181107
-
-
Zhang, Z.-H.; Yin, L.; Wang, Y.-M. Catal. Commun. 2007, 8, 1126
-
(2007)
Catal. Commun.
, vol.8
, pp. 1126
-
-
Zhang, Z.-H.1
Yin, L.2
Wang, Y.-M.3
-
12
-
-
77953947336
-
-
Patil, A. V.; Lee, S. H.; Bandgar, B. P. Bull. Korean Chem. Soc. 2010, 31, 1719
-
(2010)
Bull. Korean Chem. Soc.
, vol.31
, pp. 1719
-
-
Patil, A.V.1
Lee, S.H.2
Bandgar, B.P.3
-
13
-
-
34250769543
-
-
Mohammadpoor-Baltork, I.; Khosropour, A. R.; Hojati, S. F. Monatsh. Chem. 2007, 138, 663
-
(2007)
Monatsh. Chem.
, vol.138
, pp. 663
-
-
Mohammadpoor-Baltork, I.1
Khosropour, A.R.2
Hojati, S.F.3
-
14
-
-
35448929475
-
-
Mohammadpoor-Baltork, I.; Khosropour, A. R.; Hojati, S. F. Catal. Commun. 2007, 8, 1865
-
(2007)
Catal. Commun.
, vol.8
, pp. 1865
-
-
Mohammadpoor-Baltork, I.1
Khosropour, A.R.2
Hojati, S.F.3
-
15
-
-
84863610508
-
-
Jared, F. M.; Andrew, J. M.; El-Malika, J. Org. Lett. 2008, 10, 4915
-
(2008)
Org. Lett.
, vol.10
, pp. 4915
-
-
Jared, F.M.1
Andrew, J.M.2
El-Malika, J.3
-
16
-
-
78651387223
-
-
Hojati, S. F.; Maleki, B.; Beykzadeh, Z. Monatsh. Chem. 2011, 142, 87
-
(2011)
Monatsh. Chem.
, vol.142
, pp. 87
-
-
Hojati, S.F.1
Maleki, B.2
Beykzadeh, Z.3
-
17
-
-
84945966803
-
-
Mylari, B. L.; Scott, P. J.; Zembrowski, W. J. Synth. Commun. 1989, 19, 2921
-
(1989)
Synth. Commun.
, vol.19
, pp. 2921
-
-
Mylari, B.L.1
Scott, P.J.2
Zembrowski, W.J.3
-
18
-
-
53349099381
-
-
Mohammadpoor-Baltork, I.; Moghadam, M.; Tangestaninejad, S.; Mirkhani, V.; Zolfigol, M. A.; Hojati, S. F. J. Iran Chem. Soc. 2008, 5, S65
-
(2008)
J. Iran Chem. Soc.
, vol.5
, pp. 65
-
-
Mohammadpoor-Baltork, I.1
Moghadam, M.2
Tangestaninejad, S.3
Mirkhani, V.4
Zolfigol, M.A.5
Hojati, S.F.6
-
20
-
-
0037436954
-
-
Markó, I. E.; Vanherck, J.-C.; Ates, A.; Tinant, B.; Declercq, J.-P. Tetrahedron Lett. 2003, 44, 3333
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 3333
-
-
Markó, I.E.1
Vanherck, J.-C.2
Ates, A.3
Tinant, B.4
Declercq, J.-P.5
-
28
-
-
84863626265
-
-
Recently, our laboratory has developed a novel method for the synthesis of orthoesters that cannot be obtained by the Pinner protocol. It involves the electrolysis of the bis-ammonium salt derived from the corresponding diacid 31. An example is decribed in the Supporting Information. Unpublished work
-
Recently, our laboratory has developed a novel method for the synthesis of orthoesters that cannot be obtained by the Pinner protocol. It involves the electrolysis of the bis-ammonium salt derived from the corresponding diacid 31. An example is decribed in the Supporting Information. Mathot, C.; Lam, K.; Lucaccioni, F.; Markó, I. E. Unpublished work.
-
-
-
Mathot, C.1
Lam, K.2
Lucaccioni, F.3
Markó, I.E.4
-
30
-
-
0031058373
-
-
Kotani, T.; Nagaki, Y.; Ishii, A.; Konishi, Y.; Yago, H.; Suehiro, S.; Okukado, N.; Okamoto, K. J. Med. Chem. 1997, 40, 684
-
(1997)
J. Med. Chem.
, vol.40
, pp. 684
-
-
Kotani, T.1
Nagaki, Y.2
Ishii, A.3
Konishi, Y.4
Yago, H.5
Suehiro, S.6
Okukado, N.7
Okamoto, K.8
-
35
-
-
43049136611
-
-
Yao, M.-X.; Zeng, M.-H.; Zou, H.-H.; Zhou, Y.-L.; Liang, H. Dalton Trans. 2008, 18, 2428
-
(2008)
Dalton Trans.
, vol.18
, pp. 2428
-
-
Yao, M.-X.1
Zeng, M.-H.2
Zou, H.-H.3
Zhou, Y.-L.4
Liang, H.5
|