-
1
-
-
0012240506
-
The curse of opium: Requital through organic medicinal chemistry
-
Belleau, B. R. The curse of opium: Requital through organic medicinal chemistry. Chem. Can. 1980, 24-25.
-
(1980)
Chem. Can.
, pp. 24-25
-
-
Belleau, B.R.1
-
2
-
-
0001778685
-
Natural and unnatural codeine, morphine analogs
-
Phillipson, J. D., Roberts, M. F., Zenk, M., Eds.: Springer-Verlag: Berlin
-
Rice, K. C. Natural and unnatural codeine, morphine analogs. In The Chemistry and Biology of Isoquinoline Alkaloids; Phillipson, J. D., Roberts, M. F., Zenk, M., Eds.: Springer-Verlag: Berlin, 1985; pp 191-203.
-
(1985)
The Chemistry and Biology of Isoquinoline Alkaloids
, pp. 191-203
-
-
Rice, K.C.1
-
3
-
-
77957027656
-
The morphine alkaloids
-
Cordell, G. A., Brossi, A., Eds.; Academic: New York
-
Szàntay, C.; Dörnyei, G.; Blaskó, G. The morphine alkaloids. In The Alkaloids; Cordell, G. A., Brossi, A., Eds.; Academic: New York, 1994, 45, 127-232.
-
(1994)
The Alkaloids
, vol.45
, pp. 127-232
-
-
Szàntay, C.1
Dörnyei, G.2
Blaskó, G.3
-
4
-
-
0026362354
-
-
Ellis, G. P., West, G. B., Eds.; North Holland: Amsterdam
-
Schiller, P. W. In Progress in Medicinal Chemistry; Ellis, G. P., West, G. B., Eds.; North Holland: Amsterdam, 1991; Vol. 28, pp 301-340.
-
(1991)
Progress in Medicinal Chemistry
, vol.28
, pp. 301-340
-
-
Schiller, P.W.1
-
5
-
-
0030472350
-
International union of pharmacology. XII. Classification of opioid receptors
-
Dhawan, B. N.; Cesselin, F.; Raghubir, R.; Reisine, T.; Bradley, P. B.; Portoghese, P. S.; Hamon, M. International union of pharmacology. XII. Classification of opioid receptors. Pharma. Col. Rev. 1996, 48, 567-592.
-
(1996)
Pharma. Col. Rev.
, vol.48
, pp. 567-592
-
-
Dhawan, B.N.1
Cesselin, F.2
Raghubir, R.3
Reisine, T.4
Bradley, P.B.5
Portoghese, P.S.6
Hamon, M.7
-
6
-
-
0034464742
-
Uncovering molecular mechanisms involved in activation of G-protein coupled receptors
-
Gether, U. Uncovering molecular mechanisms involved in activation of G-protein coupled receptors. Endocr. Rev. 2000, 21, 90-113.
-
(2000)
Endocr. Rev.
, vol.21
, pp. 90-113
-
-
Gether, U.1
-
7
-
-
0029947902
-
A 3D model of the δ opioid receptor and ligand-receptor complex
-
Alkorta, I.; Lowe, G. H. A 3D model of the δ opioid receptor and ligand-receptor complex. Protein Eng. 1996, 9, 573-583.
-
(1996)
Protein Eng.
, vol.9
, pp. 573-583
-
-
Alkorta, I.1
Lowe, G.H.2
-
8
-
-
0031436823
-
Comparative modeling and molecular dynamics studies of the δ, κ, and μ opioid receptors
-
Strahs, D.; Weinstein, H. Comparative modeling and molecular dynamics studies of the δ, κ, and μ opioid receptors. Protein Eng. 1997, 10, 1019-1038.
-
(1997)
Protein Eng.
, vol.10
, pp. 1019-1038
-
-
Strahs, D.1
Weinstein, H.2
-
9
-
-
0031848224
-
Opioid receptor three-dimensional structures from distance geometry calculations with hydrogen bonding constraints
-
Pogozheva, I. D.; Lomize, A. L.; Mosberg, H. I. Opioid receptor three-dimensional structures from distance geometry calculations with hydrogen bonding constraints. Biophys. J. 1998, 75, 612-634.
-
(1998)
Biophys. J.
, vol.75
, pp. 612-634
-
-
Pogozheva, I.D.1
Lomize, A.L.2
Mosberg, H.I.3
-
10
-
-
0032808048
-
Molecular modeling study of the differential ligand-receptor interaction at the μ, δ and κ opioid receptors
-
Filizola, M.; Carteni-Farina, M.; Perez, J. J. Molecular modeling study of the differential ligand-receptor interaction at the μ, δ and κ opioid receptors. J. Comput.-Aided Mol. Des. 1999, 13, 397-407.
-
(1999)
J. Comput.-Aided Mol. Des.
, vol.13
, pp. 397-407
-
-
Filizola, M.1
Carteni-Farina, M.2
Perez, J.J.3
-
11
-
-
0034163432
-
Homology models of μ-opioid receptors with organic and inorganic cations at conserved aspartates in the second and third transmembrane domains
-
Zhorov, B, S.; Ananthanarayanan, V. S. Homology models of μ-opioid receptors with organic and inorganic cations at conserved aspartates in the second and third transmembrane domains. Arch. Biochem. Biophys. 2000, 375, 31-49.
-
(2000)
Arch. Biochem. Biophys.
, vol.375
, pp. 31-49
-
-
Zhorov, B.S.1
Ananthanarayanan, V.S.2
-
12
-
-
0029054001
-
Opiate receptors
-
Reisine, T. Opiate receptors. Neuropharmacology 1995, 34, 463-472.
-
(1995)
Neuropharmacology
, vol.34
, pp. 463-472
-
-
Reisine, T.1
-
13
-
-
0029949928
-
Opioid receptor types and subtypes: The δ-receptor as a model
-
Zaki, P. A.; Bilsky, T. W.; Vanderah, T. W.; Lai, J.; Evans, C. J.; Porreca, F. Opioid receptor types and subtypes: The δ-receptor as a model. Annu. Rev. Pharmacol. Toxicol. 1996, 36, 379-401.
-
(1996)
Annu. Rev. Pharmacol. Toxicol.
, vol.36
, pp. 379-401
-
-
Zaki, P.A.1
Bilsky, T.W.2
Vanderah, T.W.3
Lai, J.4
Evans, C.J.5
Porreca, F.6
-
14
-
-
0035185186
-
Molecular determinants of non-specific recognition of δ, μ and κ opioid receptors
-
Filizola, M.; Villar, H. O.; Loew, G. H. Molecular determinants of non-specific recognition of δ, μ and κ opioid receptors. Bioorg. Med. Chem. 2001, 9, 69-76.
-
(2001)
Bioorg. Med. Chem.
, vol.9
, pp. 69-76
-
-
Filizola, M.1
Villar, H.O.2
Loew, G.H.3
-
15
-
-
0028900341
-
Structure-activity relationships of synthetic and semisynthetic opioid agonists and antagonists
-
Fürst, S.; Hosztafi, S.; Friedman, T. Structure-activity relationships of synthetic and semisynthetic opioid agonists and antagonists. Curr. Med. Chem. 1995, 1, 423-440.
-
(1995)
Curr. Med. Chem.
, vol.1
, pp. 423-440
-
-
Fürst, S.1
Hosztafi, S.2
Friedman, T.3
-
16
-
-
0000092188
-
Analgesics
-
Wolff, M. E., Ed.; John Wiley & Sons: New York
-
Aldrich, J. V. Analgesics. In Burger's Medicinal Chemistry and Drug Discovery; Wolff, M. E., Ed.; John Wiley & Sons: New York, 1996; Vol. 3, pp 321-441.
-
(1996)
Burger's Medicinal Chemistry and Drug Discovery
, vol.3
, pp. 321-441
-
-
Aldrich, J.V.1
-
17
-
-
0019851303
-
Structural requirements for specific recognition of μ or δ opiate receptors
-
Fournie-Zaluski, M.-C.; Gacel, G.; Maigret, B.; Premilat, S.; Roques, B. P. Structural requirements for specific recognition of μ or δ opiate receptors. Mol. Pharmacol. 1981, 20, 484-491.
-
(1981)
Mol. Pharmacol.
, vol.20
, pp. 484-491
-
-
Fournie-Zaluski, M.-C.1
Gacel, G.2
Maigret, B.3
Premilat, S.4
Roques, B.P.5
-
18
-
-
0013800287
-
A new concept on the mode of interaction of narcotic analgesics with receptors
-
Portoghese, P. S. A new concept on the mode of interaction of narcotic analgesics with receptors. J. Med. Chem. 1965, 8, 609-616.
-
(1965)
J. Med. Chem.
, vol.8
, pp. 609-616
-
-
Portoghese, P.S.1
-
19
-
-
0000489524
-
Synthetic analgesics: Stereochemical considerations
-
Beckett, A. H.; Casy, A. F. Synthetic analgesics: Stereochemical considerations. J. Pharma: Pharmacol. 1954, 6, 986-1001.
-
(1954)
J. Pharma: Pharmacol.
, vol.6
, pp. 986-1001
-
-
Beckett, A.H.1
Casy, A.F.2
-
20
-
-
0029955277
-
Asymmetric synthesis, opioid receptor affinities, and antinociceptive effects of 8-amino-5,9-methanobenzo cyclooctenes, a new class of structural analogues of the morphine alkaloids
-
Schultz, A. G.; Wang, A.; Alva, C.; Sebastian, A.; Glick, S. D.; Deecher, D. C.; Bidlack, J. M. Asymmetric synthesis, opioid receptor affinities, and antinociceptive effects of 8-amino-5,9-methanobenzo cyclooctenes, a new class of structural analogues of the morphine alkaloids. J. Med. Chem. 1996, 39, 1956-1966.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 1956-1966
-
-
Schultz, A.G.1
Wang, A.2
Alva, C.3
Sebastian, A.4
Glick, S.D.5
Deecher, D.C.6
Bidlack, J.M.7
-
21
-
-
0034699499
-
Selective protection and functionalization of morphine: Synthesis and opioid receptor binding properties of 3-amino-3-desoxymorphine derivatives
-
Wentland, M. P.; Duan, W.; Cohen, D. J.; Bidlack, J. M. Selective protection and functionalization of morphine: Synthesis and opioid receptor binding properties of 3-amino-3-desoxymorphine derivatives. J. Med. Chem. 2000, 43, 3558-3565.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 3558-3565
-
-
Wentland, M.P.1
Duan, W.2
Cohen, D.J.3
Bidlack, J.M.4
-
22
-
-
0034743047
-
Palladium catalyzed elaboration of codeine and morphine
-
Davies, S. G.; Goodwin, C. J.; Pyatt, D.; Smith, A. D. Palladium catalyzed elaboration of codeine and morphine. J. Chem. Soc., Perkin Trans. 1 2001, 1412-1420.
-
(2001)
J. Chem. Soc., Perkin Trans 1
, pp. 1412-1420
-
-
Davies, S.G.1
Goodwin, C.J.2
Pyatt, D.3
Smith, A.D.4
-
23
-
-
0034710723
-
3-Deoxycyclocinnamox: The first high-affinity, nonpeptide μ-opioid antagonist lacking a phenolic hydroxyl group
-
Derrick, I.; Neilan, C. L.; Amdes, J.; Husbands, S.; Woods, J. H.; Traynor, J. R.; Lewis, J. W. 3-Deoxycyclocinnamox: The first high-affinity, nonpeptide μ-opioid antagonist lacking a phenolic hydroxyl group. J. Med. Chem. 2000, 43, 3348-3350.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 3348-3350
-
-
Derrick, I.1
Neilan, C.L.2
Amdes, J.3
Husbands, S.4
Woods, J.H.5
Traynor, J.R.6
Lewis, J.W.7
-
24
-
-
0024334804
-
Recent developments in the design of receptor specific opioid peptides
-
Hruby, V. J.; Gehrig, C. A. Recent developments in the design of receptor specific opioid peptides. Med. Res. Rev. 1989, 9, 343-401.
-
(1989)
Med. Res. Rev.
, vol.9
, pp. 343-401
-
-
Hruby, V.J.1
Gehrig, C.A.2
-
25
-
-
0034000876
-
Novel ligands lacking a positive charge for the δ- and μ-opioid receptors
-
Schiller, P. W.; Berezowska, I.; Nguyen, T. M.-D.; Schmidt, R.; Lemieux, C.; Chung, N. N.; Falcone-Hindley, M. L.; Yao, W.; Liu, J.; Iwama, S.; Smith, A. B., III; Hirschmann, R. Novel ligands lacking a positive charge for the δ- and μ-opioid receptors. J. Med. Chem. 2000, 43, 551-559.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 551-559
-
-
Schiller, P.W.1
Berezowska, I.2
Nguyen, T.M.-D.3
Schmidt, R.4
Lemieux, C.5
Chung, N.N.6
Falcone-Hindley, M.L.7
Yao, W.8
Liu, J.9
Iwama, S.10
Smith A.B. III11
Hirschmann, R.12
-
26
-
-
0035913055
-
Novel C-terminus. Modifications of the Dmt-Tic motif: A new class of dipeptide analogues showing altered pharmacological profiles toward the opioid receptors
-
Pagé, D.; Naismith, A.; Schmidt, R.; Coupal, M.; Labarre, M.; Gosselin, M.; Bellemare, D.; Payza, K.; Brown, W. Novel C-Terminus. Modifications of the Dmt-Tic Motif: A New Class of Dipeptide Analogues Showing Altered Pharmacological Profiles toward the Opioid Receptors. J. Med. Chem. 2001, 44, 2387-2390.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 2387-2390
-
-
Pagé, D.1
Naismith, A.2
Schmidt, R.3
Coupal, M.4
Labarre, M.5
Gosselin, M.6
Bellemare, D.7
Payza, K.8
Brown, W.9
-
27
-
-
0034694363
-
Arylacetamides as peripherally restricted kappa opioid receptor agonists
-
Kumar, V.; Marello, M. A.; Cortes-Burgos, L.; Chang, A.-C.; Cassel, J. A.; Daubert, J. D.; DeHaven, R. N.; DeHaven-Hudkins, D. L.; Gottshall, S. L.; Mansson, E.; Maycock, A. L. Arylacetamides as peripherally restricted kappa opioid receptor agonists. Bioorg. Med. Chem. Lett. 2000, 10, 2567-2570.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 2567-2570
-
-
Kumar, V.1
Marello, M.A.2
Cortes-Burgos, L.3
Chang, A.-C.4
Cassel, J.A.5
Daubert, J.D.6
DeHaven, R.N.7
DeHaven-Hudkins, D.L.8
Gottshall, S.L.9
Mansson, E.10
Maycock, A.L.11
-
28
-
-
0032901479
-
Regulation of opioid receptor activities
-
Law, P. Y.; Loh, H. H. Regulation of opioid receptor activities. J. Pharmacol. Exp. Ther. 1999, 289, 607-624.
-
(1999)
J. Pharmacol. Exp. Ther.
, vol.289
, pp. 607-624
-
-
Law, P.Y.1
Loh, H.H.2
-
29
-
-
0032428284
-
Opiate tolerance and dependence: Receptors, G-proteins, and antiopiates
-
Harrison, L. M.; Kastin, A. J.; Zadina, J. E. Opiate tolerance and dependence: Receptors, G-proteins, and antiopiates. Peptides 1998, 9, 1603-1630.
-
(1998)
Peptides
, vol.9
, pp. 1603-1630
-
-
Harrison, L.M.1
Kastin, A.J.2
Zadina, J.E.3
-
30
-
-
0032241091
-
A molecular basis for opiate action
-
Massotte, D.; Keiffer, B. L. A molecular basis for opiate action. Essays Biochem. 1998, 33, 65-77.
-
(1998)
Essays Biochem.
, vol.33
, pp. 65-77
-
-
Massotte, D.1
Keiffer, B.L.2
-
31
-
-
0001911108
-
Opioid receptors
-
Emmet, J. D., Ed.; Pergamon Press: New York
-
Rees, D. C.; Hunter, J. C. Opioid receptors. In Comprehensive Medicinal Chemistry; Emmet, J. D., Ed.; Pergamon Press: New York, 1990; pp 805-846.
-
(1990)
Comprehensive Medicinal Chemistry
, pp. 805-846
-
-
Rees, D.C.1
Hunter, J.C.2
-
32
-
-
0016724368
-
Oxilorphan and butorphamol. Potent narcotic antagonists and nonaddicting analgesics in the 3,14-dihydroxymorphinan series. Part V
-
Monkovic, I.; Wong, H.; Pircio, A. W.; Perron, Y. G.; Pachter, I. J.; Belleau, B. Oxilorphan and butorphamol. Potent narcotic antagonists and nonaddicting analgesics in the 3,14-dihydroxymorphinan series. Part V. Can. J. Chem. 1975, 53, 3094-3102.
-
(1975)
Can. J. Chem.
, vol.53
, pp. 3094-3102
-
-
Monkovic, I.1
Wong, H.2
Pircio, A.W.3
Perron, Y.G.4
Pachter, I.J.5
Belleau, B.6
-
33
-
-
0029957394
-
Cyclazocine revisited
-
Archer, S.; Glick, S. D.; Bidlack, J. M. Cyclazocine revisited. Neurochem. Res. 1996, 21, 1369-1373.
-
(1996)
Neurochem. Res.
, vol.21
, pp. 1369-1373
-
-
Archer, S.1
Glick, S.D.2
Bidlack, J.M.3
-
34
-
-
14444275713
-
-
Kosterlitz, H.W., Collier, H. O. J., Villareal, J. G., Eds.; Macmillan: New York
-
Fink, M.; Freedman, A. M.; Resnick, R.; Zaks, A. In Agonist and Antagonist Actions of Narcotic Analgesic Drugs; Kosterlitz, H. W., Collier, H. O. J., Villareal, J. G., Eds.; Macmillan: New York, 1971; pp 266-276.
-
(1971)
Agonist and Antagonist Actions of Narcotic Analgesic Drugs
, pp. 266-276
-
-
Fink, M.1
Freedman, A.M.2
Resnick, R.3
Zaks, A.4
-
35
-
-
0034677132
-
8-Aminocylclazocine analogues: Synthesis and structure activity relationships
-
Wentland, M. P.; Xu, G.; Cioffi, C. L.; Ye, Y.; Duan, W.; Cohen, D. J.; Colasurdo, A. M.; Bidlack, J. M. 8-Aminocylclazocine analogues: Synthesis and structure activity relationships. Bioorg. Med. Chem. Lett. 2000, 10, 183-187.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 183-187
-
-
Wentland, M.P.1
Xu, G.2
Cioffi, C.L.3
Ye, Y.4
Duan, W.5
Cohen, D.J.6
Colasurdo, A.M.7
Bidlack, J.M.8
-
36
-
-
0016701344
-
Identification of two pentapeptides from brain with potent opiate agonist activity
-
Hughes, J.; Smith, T. N.; Kosterlitz, H. W.; Fotthergill, L. A.; Morgen, B. A.; Morris, H. R. Identification of two pentapeptides from brain with potent opiate agonist activity. Nature 1976, 258, 577-579.
-
(1976)
Nature
, vol.258
, pp. 577-579
-
-
Hughes, J.1
Smith, T.N.2
Kosterlitz, H.W.3
Fotthergill, L.A.4
Morgen, B.A.5
Morris, H.R.6
-
37
-
-
0015789860
-
The search for a better analgesic
-
Eddy, N. B.; May, E. L. The search for a better analgesic. Science 1973, 181, 407-414.
-
(1973)
Science
, vol.181
, pp. 407-414
-
-
Eddy, N.B.1
May, E.L.2
-
38
-
-
0034687249
-
Synthesis and evaluation of N,N-Dialkyl enkephalin-based affinity labels for δ opioid receptors
-
Maeda, D. Y.; Ishmael, J. E.; Murray, T. F.; Aldrich, J. V. Synthesis and evaluation of N,N-Dialkyl enkephalin-based affinity labels for δ opioid receptors. J. Med. Chem. 2000, 43, 3941-3948.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 3941-3948
-
-
Maeda, D.Y.1
Ishmael, J.E.2
Murray, T.F.3
Aldrich, J.V.4
-
40
-
-
0017620408
-
ACTH: A short introductory review
-
Schwyzer, R. ACTH: A short introductory review. Ann. N.Y. Acad. Sci. 1977, 247, 3-26.
-
(1977)
Ann. N.Y. Acad. Sci.
, vol.247
, pp. 3-26
-
-
Schwyzer, R.1
-
41
-
-
0029994263
-
Application of the message-address concept to the docking of naltrexone and selective naltrexone-derived opioid antagonists into opioid receptor models
-
Metzger, T. G.; Paterlini, M. G.; Portoghese, P. S.; Ferguson, D. M. Application of the message-address concept to the docking of naltrexone and selective naltrexone-derived opioid antagonists into opioid receptor models. Neurochem. Res. 1996, 21, 1287-1294.
-
(1996)
Neurochem. Res.
, vol.21
, pp. 1287-1294
-
-
Metzger, T.G.1
Paterlini, M.G.2
Portoghese, P.S.3
Ferguson, D.M.4
-
42
-
-
0035811447
-
From models to molecules: Opioid receptor dimers, bivalent ligands, and selective opioid receptor probes
-
Portoghese, P. S. From models to molecules: Opioid receptor dimers, bivalent ligands, and selective opioid receptor probes. J. Med. Chem. 2001, 44, 2259-2269.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 2259-2269
-
-
Portoghese, P.S.1
-
44
-
-
0027329030
-
Synthesis and κ-opioid antagonist selectivity of a norbinaltrophimine congener. Identification of the address moiety required for κ-antagonist activity
-
Lin, C. E.; Takemori, A. E.; Portoghese, P. S. Synthesis and κ-opioid antagonist selectivity of a norbinaltrophimine congener. Identification of the address moiety required for κ-antagonist activity. J. Med. Chem. 1993, 36, 2412-2415.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 2412-2415
-
-
Lin, C.E.1
Takemori, A.E.2
Portoghese, P.S.3
-
45
-
-
0028275934
-
Structure-activity relationship of N17′-substituted norbinaltorphimine congeners. Role of the N17′ basic group in the interaction with a putative address substite on the ′-opioid receptor
-
Portoghese, P. S.; Lin, C.-E.; Farouz-Grant, F.; Takemori, A. E. Structure-activity relationship of N17′-substituted norbinaltorphimine congeners. Role of the N17′ basic group in the interaction with a putative address substite on the ′-opioid receptor. J. Med. Chem. 1994, 37, 1495-1500.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 1495-1500
-
-
Portoghese, P.S.1
Lin, C.-E.2
Farouz-Grant, F.3
Takemori, A.E.4
-
46
-
-
0029875344
-
Opioid antagonist activity of naltrexone-derived bivalent ligands: Importance of a properly oriented molecular scaffold to guide "address" recognition at ′ opioid receptors
-
Bolognesi, M. L.; Ojala, W. H.; Gleason, W. B.; Griffin, J. F.; Farouz-Grant, F.; Larson, D. L.; Takemori, A. E.; Portoghese, P. S. Opioid antagonist activity of naltrexone-derived bivalent ligands: Importance of a properly oriented molecular scaffold to guide "address" recognition at ′ opioid receptors. J. Med. Chem. 1996, 39, 1816-1822.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 1816-1822
-
-
Bolognesi, M.L.1
Ojala, W.H.2
Gleason, W.B.3
Griffin, J.F.4
Farouz-Grant, F.5
Larson, D.L.6
Takemori, A.E.7
Portoghese, P.S.8
-
47
-
-
0016195292
-
Importance of the nitrogen lone electron pair orientation in stereospecific opiates
-
Belleau, B.; Conway, T.; Ahmed, F. R.; Hardy, A. D. Importance of the nitrogen lone electron pair orientation in stereospecific opiates. J. Med. Chem. 1974, 17, 907-908.
-
(1974)
J. Med. Chem.
, vol.17
, pp. 907-908
-
-
Belleau, B.1
Conway, T.2
Ahmed, F.R.3
Hardy, A.D.4
-
48
-
-
0012310934
-
Stereoelectronic regulation of the opiate receptor: Some conceptual problems
-
Burlington House, London
-
Belleau, B. Stereoelectronic regulation of the opiate receptor: Some conceptual problems. In Chemical Regulation of Biological Mechanisms; Burlington House, London, 1982; pp 201-221.
-
(1982)
Chemical Regulation of Biological Mechanisms
, pp. 201-221
-
-
Belleau, B.1
-
49
-
-
84950084793
-
The psychobiological basis of heuristic synthesis planning-man, machine and the Chiron approach
-
Hanessian, S.; Franco, J.; Larouche, B. The psychobiological basis of heuristic synthesis planning-man, machine and the Chiron approach. Pure Appl. Chem. 1990, 62, 1887-1910.
-
(1990)
Pure Appl. Chem.
, vol.62
, pp. 1887-1910
-
-
Hanessian, S.1
Franco, J.2
Larouche, B.3
-
51
-
-
0035887408
-
Highly diastereoselective intramolecular [1,2]-stevens rearrangements-asymmetric syntheses of functionalized isopavines as morphinomimetics
-
Hanessian, S.; Mauduit, M. Highly diastereoselective intramolecular [1,2]-stevens rearrangements-asymmetric syntheses of functionalized isopavines as morphinomimetics. Angew. Chem., Int. Ed. 2001, 40, 3810-3813.
-
(2001)
Angew. Chem., Int. Ed.
, vol.40
, pp. 3810-3813
-
-
Hanessian, S.1
Mauduit, M.2
-
52
-
-
0037127854
-
Synthesis of desymmetrized, enantiopure dihydro-methano-diarylazocines-topologically interesting eyeteaser molecules
-
Hanessian, S.; Mauduit, M.; Demont, E.; Talbot, C. Synthesis of desymmetrized, enantiopure dihydro-methano-diarylazocines-topologically interesting eyeteaser molecules. Tetrahedron 2002, 58, 485-490.
-
(2002)
Tetrahedron
, vol.58
, pp. 485-490
-
-
Hanessian, S.1
Mauduit, M.2
Demont, E.3
Talbot, C.4
-
53
-
-
12444300549
-
Pavine and isopavine alkaloids
-
Academic Press: New York
-
Gözler, B. Pavine and isopavine alkaloids. In The Alkaloids; Academic Press: New York, 1987; Vol. 31, pp 317-389.
-
(1987)
The Alkaloids
, vol.31
, pp. 317-389
-
-
Gözler, B.1
-
54
-
-
0000033512
-
The stevens and related rearrangements
-
Trost, B. M., Fleming, I., Pattenden, I., Eds.; Pergamon: New York
-
Markó, I. E. The stevens and related rearrangements. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Pattenden, I., Eds.; Pergamon: New York, 1991; Vol. 3, pp 913-973.
-
(1991)
Comprehensive Organic Synthesis
, vol.3
, pp. 913-973
-
-
Markó, I.E.1
-
55
-
-
37049158339
-
Degradation of quaternary ammonium salts part I
-
Stevens, T. S.; Creighton, E. M.; Gordon, A. B.; Macnicol, M. Degradation of Quaternary Ammonium Salts Part I. J. Chem. Soc. 1928, 3193-3197.
-
(1928)
J. Chem. Soc.
, pp. 3193-3197
-
-
Stevens, T.S.1
Creighton, E.M.2
Gordon, A.B.3
Macnicol, M.4
-
56
-
-
0032489407
-
Diastereoselective synthesis of γ-hydroxy-β-amino alcohols and (2S,3S)-β-hydroxyleucine from chiral D-(N,N-dibenzylamino)serine (TBDMS) aldehyde
-
Laib, T.; Chastanet, J.; Zhu, J. Diastereoselective synthesis of γ-hydroxy-β-amino alcohols and (2S,3S)-β-hydroxyleucine from chiral D-(N,N-dibenzylamino)serine (TBDMS) aldehyde. J. Org. Chem. 1998, 63, 1709-1713.
-
(1998)
J. Org. Chem.
, vol.63
, pp. 1709-1713
-
-
Laib, T.1
Chastanet, J.2
Zhu, J.3
-
57
-
-
33947295106
-
Synthesis of isoquinolines. XI. Dibenzo [c,f]-1-azabicyclo[3.3.1]nonanes and 4-Phenyl-1,2,3,4-tetrahydroisoquinolines
-
Bobbitt, J. M.; Shibuya, S. Synthesis of isoquinolines. XI. Dibenzo [c,f]-1-azabicyclo[3.3.1]nonanes and 4-Phenyl-1,2,3,4-tetrahydroisoquinolines. J. Org. Chem. 1970, 35, 1181-1183.
-
(1970)
J. Org. Chem.
, vol.35
, pp. 1181-1183
-
-
Bobbitt, J.M.1
Shibuya, S.2
-
58
-
-
0000275145
-
A general synthesis of dibenz[c,f]-1-aza-bicyclo[3.3.1]-nonane and Its related compounds
-
Takayama, H.; Takamoto, M.; Okamoto, T. A General Synthesis of Dibenz[c,f]-1-aza-bicyclo[3.3.1]-nonane and Its Related Compounds. Tetrahedron Lett. 1978, 1307-1308.
-
(1978)
Tetrahedron Lett.
, pp. 1307-1308
-
-
Takayama, H.1
Takamoto, M.2
Okamoto, T.3
-
59
-
-
0014236620
-
Synthesis and pharmacological properties of N-derivatives of 5,6-dihydro-7h,12h-dibenz[c,f]azocine, a new tricyclic system
-
Casadio, S.; Pala, G.; Crescenzi, E.; Marazzi-Uberti, E.; Coppi, G.; Turba, C. Synthesis and pharmacological properties of N-derivatives of 5,6-dihydro-7H,12H-dibenz[c,f]azocine, a new tricyclic system. J. Med. Chem. 1968, 11, 97-100.
-
(1968)
J. Med. Chem.
, vol.11
, pp. 97-100
-
-
Casadio, S.1
Pala, G.2
Crescenzi, E.3
Marazzi-Uberti, E.4
Coppi, G.5
Turba, C.6
-
60
-
-
0001163453
-
Base-induced reactions of N-methyl quaternary salts of 1-Aza-dibenzo[c,f]bicyclo[3.3.1]nona-3,6-diene and related compounds
-
Takayama, H.; Nomoto, T.; Suzuki, T.; Takamoto, M.; Okamoto, T. Base-induced reactions of N-methyl quaternary salts of 1-Aza-dibenzo[c,f]bicyclo[3.3.1]nona-3,6-diene and related compounds. Heterocycles 1978, 9, 1545-1548.
-
(1978)
Heterocycles
, vol.9
, pp. 1545-1548
-
-
Takayama, H.1
Nomoto, T.2
Suzuki, T.3
Takamoto, M.4
Okamoto, T.5
-
61
-
-
0029017726
-
1A receptor interactions
-
1A receptor interactions. J. Med. Chem. 1995, 38, 647-658.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 647-658
-
-
Hedberg, M.H.1
Johansson, A.M.2
Nordvall, G.3
Yliniemelä, A.4
Li, H.B.5
Martin, A.R.6
Hjorth, S.7
Unelius, L.8
Sundell, S.9
Hacksell, U.10
-
62
-
-
0029743317
-
An improved catalyst system for aromartic carbon-nitrogen bond formation: The possible involvement of Bis(phosphine)palladium complexes as key intermediates
-
Wolfe, J. P.; Wagan, S.; Buchwald, S. L. An improved catalyst system for aromartic carbon-nitrogen bond formation: The possible involvement of Bis(phosphine)palladium complexes as key intermediates. J. Am. Chem. Soc. 1996, 118, 7215-7216.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 7215-7216
-
-
Wolfe, J.P.1
Wagan, S.2
Buchwald, S.L.3
-
63
-
-
0012344777
-
Catalytic N-dealkylation of tertiary amines: A biomimetic oxygenation reaction
-
Chaudhuri, N. K.; Servando, O.; Markus, B.; Galynker, I.; Sung, M. S. Catalytic N-dealkylation of tertiary amines: A biomimetic oxygenation reaction. J. Indian Chem. Soc. Soc. 1985, 62, 899-903.
-
(1985)
J. Indian Chem. Soc. Soc.
, vol.62
, pp. 899-903
-
-
Chaudhuri, N.K.1
Servando, O.2
Markus, B.3
Galynker, I.4
Sung, M.S.5
-
64
-
-
0012283569
-
Pavinane and isopavinane alkaloids. Correlation of absolute configurations by synthesis
-
Dyke, S. F.; Kinsman, R. G.; Warner, P.; White, A. W. C. Pavinane and isopavinane alkaloids. Correlation of absolute configurations by synthesis. Tetrahedron 1978, 34, 241-245.
-
(1978)
Tetrahedron
, vol.34
, pp. 241-245
-
-
Dyke, S.F.1
Kinsman, R.G.2
Warner, P.3
White, A.W.C.4
-
65
-
-
0023604655
-
Asymmetric synthesis of isoquinoline alkaloids
-
Meyers, A. I.; Dickman, D. A.; Boes, M. Asymmetric synthesis of isoquinoline alkaloids. Tetrahedron 1987, 43, 5095-5108.
-
(1987)
Tetrahedron
, vol.43
, pp. 5095-5108
-
-
Meyers, A.I.1
Dickman, D.A.2
Boes, M.3
-
66
-
-
0030847794
-
A simple efficient synthetic route to chiral isopavines. Synthesis of (-)-O-Methylthalisopavine and (-)-Amurensinine
-
Canillo, L.; Badiá, D.; Dominguez, E.; Vicario, J. L.; Tellitu, I. A Simple and Efficient Synthetic Route to Chiral Isopavines. Synthesis of (-)-O-Methylthalisopavine and (-)-Amurensinine. J. Org. Chem. 1997, 62, 6716-6712,
-
(1997)
J. Org. Chem.
, vol.62
, pp. 6716-6712
-
-
Canillo, L.1
Badiá, D.2
Dominguez, E.3
Vicario, J.L.4
Tellitu, I.5
-
67
-
-
0001648333
-
Synthesis of an isopavine alkaloid. (±)-O-Methylthalisopavine
-
Elliott, I. W., Jr. Synthesis of an isopavine alkaloid. (±)-O-Methylthalisopavine. J. Org. Chem. 1979, 44, 1162-1163.
-
(1979)
J. Org. Chem.
, vol.44
, pp. 1162-1163
-
-
Elliott I.W., Jr.1
-
68
-
-
37049093541
-
Base catalyzed rearrangements involving ylid intermediates. Part 15. The mechanism of the stevens [1,2] rearrangement
-
Ollis, W. D.; Rey, M.; Sutherland, I. O. Base catalyzed rearrangements involving ylid intermediates. Part 15. The mechanism of the stevens [1,2] rearrangement. J. Chem. Soc., Perkin Trans. 1 1983, 1009-1027.
-
(1983)
J. Chem. Soc., Perkin Trans 1
, pp. 1009-1027
-
-
Ollis, W.D.1
Rey, M.2
Sutherland, I.O.3
-
69
-
-
0034687241
-
N,N-Diethyl-4-(phenylpiperidin-4-ylidenemethyl)benzamide; A novel exceptionally selective potent δ opioid receptor agonist with oral biovailability and its analogues
-
Wei, Z.-H.; Brown, W.; Takasaki, B.; Plobeck, N.; Delorme, D.; Zhou, F.; Yang, H.; Jones, P.; Gawell, L.; Gagnon, H.; Schmidt, R.; Yue, S.-Y.; Walpole, C.; Payza, K.; St-Onge, S.; Labarre, M.; Godbout, C.; Jakob, A.; Butterworth, J.; Kamassab, A.; Morin, P.-E.; Projean, D.; Ducharme, J.; Roberts, E. N,N-Diethyl-4-(phenylpiperidin-4-ylidenemethyl)benzamide; A novel exceptionally selective potent δ opioid receptor agonist with oral biovailability and its analogues. J. Med. Chem. 2000, 43, 3895-3905.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 3895-3905
-
-
Wei, Z.-H.1
Brown, W.2
Takasaki, B.3
Plobeck, N.4
Delorme, D.5
Zhou, F.6
Yang, H.7
Jones, P.8
Gawell, L.9
Gagnon, H.10
Schmidt, R.11
Yue, S.-Y.12
Walpole, C.13
Payza, K.14
St-Onge, S.15
Labarre, M.16
Godbout, C.17
Jakob, A.18
Butterworth, J.19
Kamassab, A.20
Morin, P.-E.21
Projean, D.22
Ducharme, J.23
Roberts, E.24
more..
-
71
-
-
0018764468
-
Deoxymorphines: Role of the phenolic hydroxyl group in the antinociceptive and opiate receptor interactions
-
Reiden, J.; Reich, M. F. Rice, K. C.; Jacobson, A. E.; Brossi, A. Deoxymorphines: Role of the phenolic hydroxyl group in the antinociceptive and opiate receptor interactions. J. Med. Chem. 1979, 22, 256-259.
-
(1979)
J. Med. Chem.
, vol.22
, pp. 256-259
-
-
Reiden, J.1
Reich, M.F.2
Rice, K.C.3
Jacobson, A.E.4
Brossi, A.5
-
72
-
-
0025830147
-
Mu receptor binding of some commonly used opioids and their metabolites
-
Chen, Z. R.; Irvine, R. J.; Somogyi, A. A.; Bochner, F. Mu receptor binding of some commonly used opioids and their metabolites. Life Sci. 1991, 48, 2165-2171.
-
(1991)
Life Sci
, vol.48
, pp. 2165-2171
-
-
Chen, Z.R.1
Irvine, R.J.2
Somogyi, A.A.3
Bochner, F.4
|