-
1
-
-
84946393460
-
The preparation of pyridine- and piperidine-arylacetonitriles and the alkylation products of transformation
-
Panizzon, L. The preparation of pyridine- and piperidine-arylacetonitriles and the alkylation products of transformation. Helv. Chim. Acta 1944, 27, 1748-1757.
-
(1944)
Helv. Chim. Acta
, vol.27
, pp. 1748-1757
-
-
Panizzon, L.1
-
2
-
-
0029919127
-
Synthesis and pharmacology of potential cocaine antagonists. 2. Structure-Activity relationship studies of aromatic ring-substituted methylphenidate analogs
-
Deutsch, H. M.; Shi, Q.; Gruszecka-Kowalik, E.; Schweri, M. M. Synthesis and pharmacology of potential cocaine antagonists. 2. Structure-Activity relationship studies of aromatic ring-substituted methylphenidate analogs. J. Med. Chem. 1996, 39, 1201-1209.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 1201-1209
-
-
Deutsch, H.M.1
Shi, Q.2
Gruszecka-Kowalik, E.3
Schweri, M.M.4
-
3
-
-
0022270177
-
3H]Threo-(±)-methylphenidate binding to 3,4-dihydroxyphenylethylamine uptake sites in corpus striatum: Correlation with the stimulant properties of ritalinic acid esters
-
3H]Threo-(±)-methylphenidate binding to 3,4-dihydroxyphenylethylamine uptake sites in corpus striatum: correlation with the stimulant properties of ritalinic acid esters. J. Neurochem. 1985, 45, 1062-1070.
-
(1985)
J. Neurochem.
, vol.45
, pp. 1062-1070
-
-
Schweri, M.M.1
Skolnick, P.2
Rafferty, M.F.3
Rice, K.C.4
Janowsky, A.J.5
Paul, S.M.6
-
4
-
-
0028046744
-
Binding of bromine-substituted analogs of methylphenidate to monoamine transporters
-
Pan, D.; Gatley, S. J.; Dewey, S. L.; Chen, R.; Alexoff, D. A.; Ding, Y.-S.; Fowler, J. S. Binding of bromine -substituted analogs of methylphenidate to monoamine transporters. Eur. J. Pharmacol. 1994, 264, 177-182.
-
(1994)
Eur. J. Pharmacol.
, vol.264
, pp. 177-182
-
-
Pan, D.1
Gatley, S.J.2
Dewey, S.L.3
Chen, R.4
Alexoff, D.A.5
Ding, Y.-S.6
Fowler, J.S.7
-
5
-
-
0033612351
-
Methylphenidate and cocaine have a similar in vivo potency to block dopamine transporters in the human brain
-
Volkow, N. D.; Wang, G. J.; Fowler, J. S.; Fischman, M.; Foltin, R.; Abumrad, N. N.; Gatley, S. J.; Logan, J.; Wong, C.; Gifford, A.; Ding, Y. S.; Hitzemann, R.; Pappas, N. Methylphenidate and cocaine have a similar in vivo potency to block dopamine transporters in the human brain. Life Sci. 1999, 65, 7-12.
-
(1999)
Life Sci.
, vol.65
, pp. 7-12
-
-
Volkow, N.D.1
Wang, G.J.2
Fowler, J.S.3
Fischman, M.4
Foltin, R.5
Abumrad, N.N.6
Gatley, S.J.7
Logan, J.8
Wong, C.9
Gifford, A.10
Ding, Y.S.11
Hitzemann, R.12
Pappas, N.13
-
7
-
-
0023183538
-
Pharmacology of the enantiomers of threo-methylphenidate
-
Patrick, K. S.; Caldwell, R. W.; Ferris, R. M.; Breese, G. R. Pharmacology of the enantiomers of threo-methylphenidate. J. Pharmacol. Exp. Ther. 1987, 241, 152-158.
-
(1987)
J. Pharmacol. Exp. Ther.
, vol.241
, pp. 152-158
-
-
Patrick, K.S.1
Caldwell, R.W.2
Ferris, R.M.3
Breese, G.R.4
-
8
-
-
0030941402
-
11C]D-threo and L-threo-methylphenidate in the human and baboon brain
-
11C]D-threo and L-threo-methylphenidate in the human and baboon brain. Psychopharmacology (Berlin) 1997, 131, 71-78.
-
(1997)
Psychopharmacology (Berlin)
, vol.131
, pp. 71-78
-
-
Ding, Y.S.1
Fowler, J.S.2
Volkow, N.D.3
Dewey, S.L.4
Wang, G.J.5
Logan, J.6
Gatlet, S.J.7
Pappas, N.8
-
9
-
-
0034665562
-
A convenient method for synthesis of optically active methylphenidate from N-methoxycarbonylpiperidine by utilizing electrochemical oxidation and Evans aldol-type reaction
-
Matsumura, Y.; Kanda, Y.; Shirai, K.; Onomura, O.; Maki, T. A convenient method for synthesis of optically active methylphenidate from N-methoxycarbonylpiperidine by utilizing electrochemical oxidation and Evans aldol-type reaction. Tetrahedron 2000, 56, 7411-7422.
-
(2000)
Tetrahedron
, vol.56
, pp. 7411-7422
-
-
Matsumura, Y.1
Kanda, Y.2
Shirai, K.3
Onomura, O.4
Maki, T.5
-
10
-
-
0033553990
-
Enantioselective synthesis of D-threo-methylphenidate
-
Axten, J. M.; Ivy, R.; Krim, L.; Winkler, J. D. Enantioselective synthesis of D-threo-methylphenidate. J. Am. Chem. Soc. 1999, 121, 6511-6512.
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 6511-6512
-
-
Axten, J.M.1
Ivy, R.2
Krim, L.3
Winkler, J.D.4
-
11
-
-
0032567407
-
A stereoselective synthesis of DL-threo-methylphenidate: Preparation and biological evaluation of novel analogues
-
Axten, J. M.; Krim, L.; Kung, H. F.; Winkler, J. D. A stereoselective synthesis of DL-threo-methylphenidate: preparation and biological evaluation of novel analogues. J. Org. Chem. 1998, 63, 9628-9629.
-
(1998)
J. Org. Chem.
, vol.63
, pp. 9628-9629
-
-
Axten, J.M.1
Krim, L.2
Kung, H.F.3
Winkler, J.D.4
-
12
-
-
0033525482
-
The first enantioselective synthesis of (2R,2′R)-threo-(+)-methylphenidate hydrochloride
-
Prashad, M.; Kim, H.-Y.; Lu, Y.; Liu, Y.; Har, D.; Repic, O.; Blacklock, T. J.; Giannousis, P. The first enantioselective synthesis of (2R,2′R)-threo-(+)-methylphenidate hydrochloride. J. Org. Chem. 1999, 64, 1750-1753.
-
(1999)
J. Org. Chem.
, vol.64
, pp. 1750-1753
-
-
Prashad, M.1
Kim, H.-Y.2
Lu, Y.3
Liu, Y.4
Har, D.5
Repic, O.6
Blacklock, T.J.7
Giannousis, P.8
-
13
-
-
84886640510
-
3H]dopamine uptake
-
3H]dopamine uptake. Eur. J. Pharmacol. 1985, 108, 187-191.
-
(1985)
Eur. J. Pharmacol.
, vol.108
, pp. 187-191
-
-
Janowsky, A.1
Schweri, M.M.2
Berger, P.3
Long, R.4
Skolnick, P.5
Paul, S.M.6
-
14
-
-
0029875120
-
Affinities of methylphenidate derivatives for dopamine, norepinephrine and serotonin transporters
-
Gatley, S. J.; Pan, D.; Chen, R.; Chaturverdi, G.; Ding, Y. S. Affinities of methylphenidate derivatives for dopamine, norepinephrine and serotonin transporters. Life Sci. 1996, 58, 231-239.
-
(1996)
Life Sci.
, vol.58
, pp. 231-239
-
-
Gatley, S.J.1
Pan, D.2
Chen, R.3
Chaturverdi, G.4
Ding, Y.S.5
-
15
-
-
0030837830
-
2-Carbomethoxy-3-aryl-8-oxabicyclo-[3.2.1]octanes: Potent non-nitrogen inhibitors of monoamine transporters
-
Meltzer, P. C.; Liang, A. Y.; Blundell, P.; Gonzalez, M. D.; Chen, Z.; George, C.; Madras, B. K. 2-Carbomethoxy-3-aryl-8-oxabicyclo-[3.2.1]octanes: Potent non-nitrogen inhibitors of monoamine transporters. J. Med. Chem. 1997, 40, 2661-2673.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 2661-2673
-
-
Meltzer, P.C.1
Liang, A.Y.2
Blundell, P.3
Gonzalez, M.D.4
Chen, Z.5
George, C.6
Madras, B.K.7
-
16
-
-
0029965036
-
Nitrogen-based drugs are not essential for blockade of monoamine transporters
-
Madras, B. K.; Pristupa, Z. B.; Niznik, H. B.; Liang, A. Y.; Blundell, P.; Gonzalez, M. D.; Meltzer, P. C. Nitrogen-based drugs are not essential for blockade of monoamine transporters. Synapse 1996, 24, 340-348.
-
(1996)
Synapse
, vol.24
, pp. 340-348
-
-
Madras, B.K.1
Pristupa, Z.B.2
Niznik, H.B.3
Liang, A.Y.4
Blundell, P.5
Gonzalez, M.D.6
Meltzer, P.C.7
-
17
-
-
0034632801
-
2-Carbomethoxy-3-aryl-8-bicyclo-[3.2.1]octanes: Potent non-nitrogen inhibitors of monoamine transporters
-
Meltzer, P. C.; Blundell, P.; Yong, Y. F.; Chen, Z.; George, C.; Gonzalez, M. D.; Madras, B. K. 2-Carbomethoxy-3-aryl-8-bicyclo-[3.2.1]octanes: Potent non-nitrogen inhibitors of monoamine transporters. J. Med. Chem. 2000, 43, 2982-2991.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 2982-2991
-
-
Meltzer, P.C.1
Blundell, P.2
Yong, Y.F.3
Chen, Z.4
George, C.5
Gonzalez, M.D.6
Madras, B.K.7
-
18
-
-
0031833849
-
Structure activity relationships of inhibition of the dopamine transporter by 3-arylbicyclo [3.2.1] octanes
-
Meltzer, P. C.; Blundell, P.; Madras, B. K. Structure activity relationships of inhibition of the dopamine transporter by 3-arylbicyclo [3.2.1] octanes. Med. Chem. Res. 1998, 8, 12-34.
-
(1998)
Med. Chem. Res.
, vol.8
, pp. 12-34
-
-
Meltzer, P.C.1
Blundell, P.2
Madras, B.K.3
-
21
-
-
0034607295
-
Catalytic asymmetric C-II activation of alkanes and tetrahydrofuran
-
Davies, H. M. L.; Hansen, T.; Churchill, M. R. Catalytic asymmetric C-II activation of alkanes and tetrahydrofuran. J. Am. Chem. Soc. 2000, 122, 3063-3070.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 3063-3070
-
-
Davies, H.M.L.1
Hansen, T.2
Churchill, M.R.3
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