-
1
-
-
0028598490
-
-
Stratmann, K.; Burgoyne, D. L.; Moore, R. E.; Petterson, G. M. L.; Smith, C. H. J. Org. Chem. 1994, 59, 7219-7226.
-
(1994)
J. Org. Chem.
, vol.59
, pp. 7219-7226
-
-
Stratmann, K.1
Burgoyne, D.L.2
Moore, R.E.3
Petterson, G.M.L.4
Smith, C.H.5
-
3
-
-
33744702044
-
-
Ghosh, A. K.; Liu, W.; Xu, Y.; Chen, Z. Angew. Chem., Int. Ed. Engl. 1996, 35, 74-76.
-
(1996)
Angew. Chem., Int. Ed. Engl.
, vol.35
, pp. 74-76
-
-
Ghosh, A.K.1
Liu, W.2
Xu, Y.3
Chen, Z.4
-
4
-
-
0033136062
-
-
Wagner, B.; Gonzales, G. I.; Dau, M. E. T. H.; Zhu, J. Bioorg. Med Chem. 1999, 7, 737-747.
-
(1999)
Bioorg. Med Chem.
, vol.7
, pp. 737-747
-
-
Wagner, B.1
Gonzales, G.I.2
Dau, M.E.T.H.3
Zhu, J.4
-
6
-
-
0026470597
-
-
Hirschmann, R.; Nicolaou, K. C.; Pietranico, S.; Salvino, J.; Leahy, E. M.; Sprengeler, P. A.; Furst, G.; Smith, A. B.; Strader, C. D.; Cascieri, M. A.; Candelore, M. R.; Donaldson, C.; Vale, W.; Maechler, L. J. Am. Chem. Soc. 1992, 114, 9217-9218.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 9217-9218
-
-
Hirschmann, R.1
Nicolaou, K.C.2
Pietranico, S.3
Salvino, J.4
Leahy, E.M.5
Sprengeler, P.A.6
Furst, G.7
Smith, A.B.8
Strader, C.D.9
Cascieri, M.A.10
Candelore, M.R.11
Donaldson, C.12
Vale, W.13
Maechler, L.14
-
7
-
-
0032510391
-
-
Dinh, T. Q.; Smith, C. D.; Du, X.; Armstrong, R. W. J. Med. Chem. 1998, 41, 981-987.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 981-987
-
-
Dinh, T.Q.1
Smith, C.D.2
Du, X.3
Armstrong, R.W.4
-
8
-
-
0029795238
-
-
(a) Dinh, T. Q.; Du, X. H.; Armstrong, R. W. J. Org. Chem. 1996, 61, 6606-6616.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 6606-6616
-
-
Dinh, T.Q.1
Du, X.H.2
Armstrong, R.W.3
-
9
-
-
0030565527
-
-
(b) Wagner, B.; Beugelmans, R.; Zhu, J. P. Tetrahedron Lett. 1996, 37, 6557-6560.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 6557-6560
-
-
Wagner, B.1
Beugelmans, R.2
Zhu, J.P.3
-
10
-
-
0030951560
-
-
Dinh, T. Q.; Smith, C. D.; Armstrong, R. W. J. Org. Chem. 1997, 62, 790-791.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 790-791
-
-
Dinh, T.Q.1
Smith, C.D.2
Armstrong, R.W.3
-
11
-
-
0030761540
-
-
Dinh, T. Q.; Du, X. H.; Smith, C. D.; Armstrong, R. W. J. Org. Chem. 1997, 62, 6773-6783.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 6773-6783
-
-
Dinh, T.Q.1
Du, X.H.2
Smith, C.D.3
Armstrong, R.W.4
-
12
-
-
0033136062
-
-
(e) Wagner, B.; Gonzales, G. I.; Dau, M. E. T. H.; Zhu, J. Bioorg. Med. Chem. 1999, 7, 737-747.
-
(1999)
Bioorg. Med. Chem.
, vol.7
, pp. 737-747
-
-
Wagner, B.1
Gonzales, G.I.2
Dau, M.E.T.H.3
Zhu, J.4
-
13
-
-
0033532710
-
-
(f) O'Connell, C. E.; Salvato, K. A.; Meng, Z. Y.; Littlefield, B. A.; Schwartz, C. E. Bioorg. Med. Chem. Lett. 1999, 9, 1541-1546.
-
(1999)
Bioorg. Med. Chem. Lett.
, vol.9
, pp. 1541-1546
-
-
O'Connell, C.E.1
Salvato, K.A.2
Meng, Z.Y.3
Littlefield, B.A.4
Schwartz, C.E.5
-
14
-
-
26344441971
-
-
(a) Nevole, J. Chem. Ber. 1944-46, 77-79, 61.
-
(1944)
Chem. Ber.
, vol.77-79
, pp. 61
-
-
Nevole, J.1
-
16
-
-
0029127055
-
-
For conceptually related applications of "centroid" scaffolds, see the following. (a) For Kemp's triacid: Kocis, P.; Issakova, O.; Sepetov, N. F.; Lebl, M. Tetrahedon Lett. 1995, 36, 6623-6626.
-
(1995)
Tetrahedon Lett.
, vol.36
, pp. 6623-6626
-
-
Kocis, P.1
Issakova, O.2
Sepetov, N.F.3
Lebl, M.4
-
17
-
-
0030072662
-
-
(b) For 3-amino-5-hydroxybenzoic acid: Dankwardt, S. M.; Phan, T. M.; Krstenansky, J. L. Mol. Diversity 1995, 1, 113.
-
(1995)
Mol. Diversity
, vol.1
, pp. 113
-
-
Dankwardt, S.M.1
Phan, T.M.2
Krstenansky, J.L.3
-
19
-
-
0032560832
-
-
For 3,5-diaminobenzoic acid: Neustadt, B. R.; Smith, E.; Nechuta, T.; Zhang, Y. Tetrahedron Lett. 1998, 39, 5317-5320.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 5317-5320
-
-
Neustadt, B.R.1
Smith, E.2
Nechuta, T.3
Zhang, Y.4
-
20
-
-
0039279158
-
-
Epton, R., Ed.; Mayflower Scientific Ltd: Kingswinford, U.K.
-
(a) Jensen, K. J.; Songster, M. F.; Vágner, J.; Alsina, J.; Albericio, F.; Barany, G. In Innovation and Perspectives in Solid-Phase Synthesis & Combinatorial Chemical Libraries, 1996, Collected Papers, Fourth International Symposium; Epton, R., Ed.; Mayflower Scientific Ltd: Kingswinford, U.K., 1996; pp 187-190.
-
(1996)
Innovation and Perspectives in Solid-Phase Synthesis & Combinatorial Chemical Libraries, 1996, Collected Papers, Fourth International Symposium
, pp. 187-190
-
-
Jensen, K.J.1
Songster, M.F.2
Vágner, J.3
Alsina, J.4
Albericio, F.5
Barany, G.6
-
21
-
-
0032503569
-
-
(b) Jensen, K. J.; Alsina, J.; Songster, M. F.; Vágner, J.; Albericio, F.; Barany, G. J. Am. Chem. Soc. 1998, 720, 5441-5452.
-
(1998)
J. Am. Chem. Soc.
, vol.720
, pp. 5441-5452
-
-
Jensen, K.J.1
Alsina, J.2
Songster, M.F.3
Vágner, J.4
Albericio, F.5
Barany, G.6
-
22
-
-
0032823018
-
-
For a review, see: Alsina, J., Jensen, K. J.; Albericio, F.; Barany, G. Chem. Eur. J. 1999, 5, 2787-2795.
-
(1999)
Chem. Eur. J.
, vol.5
, pp. 2787-2795
-
-
Alsina, J.1
Jensen, K.J.2
Albericio, F.3
Barany, G.4
-
23
-
-
0000546098
-
-
For a study of methods for monoreduction of dinitrobenzenes, see: Terpko, M. O.; Heck, R. F. J. Org. Chem. 1980, 45, 4992-4993.
-
(1980)
J. Org. Chem.
, vol.45
, pp. 4992-4993
-
-
Terpko, M.O.1
Heck, R.F.2
-
24
-
-
0025032015
-
-
Albericio, F.; Kneib-Cordonier, N.; Biancalana, S.; Gera, L.; Masada, R. I.; Hudson, D.; Barany, G. J. Org. Chem. 1990, 55, 3730-3743.
-
(1990)
J. Org. Chem.
, vol.55
, pp. 3730-3743
-
-
Albericio, F.1
Kneib-Cordonier, N.2
Biancalana, S.3
Gera, L.4
Masada, R.I.5
Hudson, D.6
Barany, G.7
-
25
-
-
0041057955
-
-
Reduction of the nitro group without prior methoxide treatment yielded several products by HPLC
-
Reduction of the nitro group without prior methoxide treatment yielded several products by HPLC.
-
-
-
-
26
-
-
0029361890
-
-
2, (a) in solution: Meyers, H. V.; Dilley, G. J.; Durgin, T. L.; Powers, T. S.; Winssinger, N. A.; Zhu, H.; Pavia, M. R. Mol. Diversity 1995, 1, 13-20.
-
(1995)
Mol. Diversity
, vol.1
, pp. 13-20
-
-
Meyers, H.V.1
Dilley, G.J.2
Durgin, T.L.3
Powers, T.S.4
Winssinger, N.A.5
Zhu, H.6
Pavia, M.R.7
-
27
-
-
0030569368
-
-
(b) On solid phase: Mayer, J. P.; Zhang, J.; Bjergarde, K.; Lenz, D. M.; Gaudino, J. J. Tetrahedron Lett. 1996, 37, 8081-8084.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 8081-8084
-
-
Mayer, J.P.1
Zhang, J.2
Bjergarde, K.3
Lenz, D.M.4
Gaudino, J.J.5
-
28
-
-
0040463917
-
-
Formation of PyBOP' ed byproduct 4 could be due to use of more dry DMF for the library synthesis or a more concentrated coupling solution
-
Formation of PyBOP' ed byproduct 4 could be due to use of more dry DMF for the library synthesis or a more concentrated coupling solution.
-
-
-
-
29
-
-
0041057956
-
-
After completion of the library synthesis, we observed that mild treatment with 2-methyl-1-aminopropane in DMF for 30 min also removed the O-modification
-
After completion of the library synthesis, we observed that mild treatment with 2-methyl-1-aminopropane in DMF for 30 min also removed the O-modification.
-
-
-
|