-
1
-
-
0023152733
-
-
Lehmann, J.; Schneider, J.; McPherson, S.; Murphy, D. E.; Bernard, P.; Tsai, C.; Bennett, D. A.; Pastor, G.; Steel, D. J.; Boehm, C.; Cheney, D. L.; Liebman, J. M.; Williams, M.; Wood, P. L. J. Pharmacol. Exp. Ther. 1987, 240, 737-746.
-
(1987)
J. Pharmacol. Exp. Ther.
, vol.240
, pp. 737-746
-
-
Lehmann, J.1
Schneider, J.2
McPherson, S.3
Murphy, D.E.4
Bernard, P.5
Tsai, C.6
Bennett, D.A.7
Pastor, G.8
Steel, D.J.9
Boehm, C.10
Cheney, D.L.11
Liebman, J.M.12
Williams, M.13
Wood, P.L.14
-
2
-
-
0027969994
-
-
Dorsey, B. D.; Levin, R. B.; McDaniel, S. L.; Vacca, J. P.; Guare, J. P; Darke, P.L.; Zugay, J. A.; Emini, E. A.; Schleif, W. A.; Quintero, J. C.; Lin, J. H.; Chen, I.-W.; Holloway, M. K.; Fitzgerald, P. M. D.; Axel, M. G.; Ostovic, D.; Anderson, P. S.; Huff, J. R. J. Med. Chem. 1994, 37, 3443-51.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 3443-3451
-
-
Dorsey, B.D.1
Levin, R.B.2
McDaniel, S.L.3
Vacca, J.P.4
Guare, J.P.5
Darke, P.L.6
Zugay, J.A.7
Emini, E.A.8
Schleif, W.A.9
Quintero, J.C.10
Lin, J.H.11
Chen, I.-W.12
Holloway, M.K.13
Fitzgerald, P.M.D.14
Axel, M.G.15
Ostovic, D.16
Anderson, P.S.17
Huff, J.R.18
-
3
-
-
84981835642
-
-
(a) Felder, E.; Maffei, S.; Pietra, S.; Pitre, D. Helv. Chim. Acta 1960, 43, 888-896L;
-
(1960)
Helv. Chim. Acta
, vol.43
-
-
Felder, E.1
Maffei, S.2
Pietra, S.3
Pitre, D.4
-
4
-
-
0030947103
-
-
(b) Stingl, K.; Kottenhahn, M.; Drauz, K. Tetrahedron: Asymmetry 1997, 8, 979-982.
-
(1997)
Tetrahedron: Asymmetry
, vol.8
, pp. 979-982
-
-
Stingl, K.1
Kottenhahn, M.2
Drauz, K.3
-
5
-
-
0024349541
-
-
Aebischer, B.; Frey, P.; Haerter, H.-P.; Herrling, P. L.; Mueller, W.; Olverman, H. J.; Watkins, J. C. Helv. Chim. Acta 1989, 72, 1043-1051.
-
(1989)
Helv. Chim. Acta
, vol.72
, pp. 1043-1051
-
-
Aebischer, B.1
Frey, P.2
Haerter, H.-P.3
Herrling, P.L.4
Mueller, W.5
Olverman, H.J.6
Watkins, J.C.7
-
6
-
-
0029115511
-
-
Bruce, M. A.; St. Laurent, D. R.; Poindexter, G. S.; Monkovic, I.; Huang, S.; Balasubramanian, N. Synth. Commun. 1995, 25, 2673-2684.
-
(1995)
Synth. Commun.
, vol.25
, pp. 2673-2684
-
-
Bruce, M.A.1
St Laurent, D.R.2
Poindexter, G.S.3
Monkovic, I.4
Huang, S.5
Balasubramanian, N.6
-
7
-
-
0028226652
-
-
A synthesis of optically active 5-alkylpiperazine-2-carboxylic acids was reported recently: Falorni, M.; Giacomelli, G.; Satta, M.; Cossu, S. Synthesis 1994, 4, 391-395.
-
(1994)
Synthesis
, vol.4
, pp. 391-395
-
-
Falorni, M.1
Giacomelli, G.2
Satta, M.3
Cossu, S.4
-
8
-
-
0022354620
-
-
(a) Arnold, L. D.; Kalantar, T. H.; Vederas, J. C. J. Am. Chem. Soc. 1985, 107, 7105-7109.
-
(1985)
J. Am. Chem. Soc.
, vol.107
, pp. 7105-7109
-
-
Arnold, L.D.1
Kalantar, T.H.2
Vederas, J.C.3
-
9
-
-
0000242199
-
-
(b) Arnold, L. D.; Drover, J. C. G.; Vederas, J. C. J. Am. Chem. Soc. 1987, 109, 4649-4659.
-
(1987)
J. Am. Chem. Soc.
, vol.109
, pp. 4649-4659
-
-
Arnold, L.D.1
Drover, J.C.G.2
Vederas, J.C.3
-
10
-
-
0002558905
-
-
(c) Pansare, S. V.; Huyer, G.; Arnold, L. D.; Vederas, J. C. Org. Synth. 1991, 70, 1-17.
-
(1991)
Org. Synth.
, vol.70
, pp. 1-17
-
-
Pansare, S.V.1
Huyer, G.2
Arnold, L.D.3
Vederas, J.C.4
-
12
-
-
0000922307
-
-
(b) Kucharczyk, N.; Badet, B.; Le Goffic, F. Synth. Commun. 1989, 19, 1603-1609 .
-
(1989)
Synth. Commun.
, vol.19
, pp. 1603-1609
-
-
Kucharczyk, N.1
Badet, B.2
Le Goffic, F.3
-
13
-
-
33845279211
-
-
(a) Zydowsky, T. M.; Dellaria, J. F.; Nellans, H. N. J. Org. Chem. 1988, 53, 5607-5616.
-
(1988)
J. Org. Chem.
, vol.53
, pp. 5607-5616
-
-
Zydowsky, T.M.1
Dellaria, J.F.2
Nellans, H.N.3
-
16
-
-
0030014161
-
-
(d) Parr, I. B.; Boehlein, S. K.; Dribben, A. B.; Schuster, S. M.; Richards, N. G. J. J. Med. Chem. 1996, 39, 2367-2378.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 2367-2378
-
-
Parr, I.B.1
Boehlein, S.K.2
Dribben, A.B.3
Schuster, S.M.4
Richards, N.G.J.5
-
17
-
-
1542413072
-
-
note
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Unless otherwise noted, starting materials were obtained from commercial suppliers and used without further purification. The melting points of all compounds were recorded on a Mel-Temp apparatus without calibration. Infrared (IR) spectra were determined on a FT-IR spectrometer. Nuclear magnetic resonance (NMR) spectra were recorded on a 300 MHz spectrometer. Thin layer chromatography (TLC) analyses were carried out on silica gel plates.
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