-
1
-
-
85022929235
-
Racemic material, the resolved (+)-enantiomer showed twice the activity as compared to the racemic compound
-
Racemic material, the resolved (+)-enantiomer showed twice the activity as compared to the racemic compound.
-
-
-
-
2
-
-
85022920270
-
Preliminary results of this paper were presented
-
Los Angeles, CA, September MEDI 108
-
Preliminary results of this paper were presented: Sit, S. Y.; Parker, R. A.; Brown, P. J.; Balasubramanian, N.; Catt, J. D.; Harte, W. E.; Motoc, I. I.; Wright, J. J. The 196th National Meeting of the American Chemical Society, Los Angeles, CA, September 26–30, 1988, MEDI 108.
-
(1988)
The 196th National Meeting of the American Chemical Society
, pp. 26-30
-
-
Sit, S.Y.1
Parker, R.A.2
Brown, P.J.3
Balasubramanian, N.4
Catt, J.D.5
Harte, W.E.6
Motoc, I.I.7
Wright, J.J.8
-
4
-
-
85022951020
-
The 197th National Meeting of the American Chemical Society
-
Other analogues of BMY 21950 Dallas, TX, April 9-14 MEDI 16
-
Other analogues of BMY 21950: Brown, P. J.; Balasubramanian, N.; Catt, J. D.; Sit, S. Y.; Harte, W. E.; Parker, R. A.; Wright, J. J. The 197th National Meeting of the American Chemical Society, Dallas, TX, April 9-14, 1989, MEDI 16.
-
(1989)
-
-
Brown, P.J.1
Balasubramanian, N.2
Catt, J.D.3
Sit, S.Y.4
Harte, W.E.5
Parker, R.A.6
Wright, J.J.7
-
5
-
-
0024465415
-
-
Balasubramanian, N.; Brown, P. J.; Catt, J. D.; Han, W. T.; Parker, R. A.; Sit, S. Y.; Wright, J. J. J. Med. Chem. 1989, 32, 2038.
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Brown, P.J.2
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Sit, S.Y.6
Wright, J.J.7
-
6
-
-
0023121401
-
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Anderson, K. M.; Castelli, W. P.; Levy, D. JAMA, J. Am. Med. Assoc. 1987, 257 (16), 2176.
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Anderson, K.M.1
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10
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0003899587
-
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and references therein
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Lee, T.-J. Trends Pharm. Sci. 1987, 8, 443 and references therein.
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-
Lee, T.-J.1
-
11
-
-
85022967160
-
Stereospecific synthesis of the 3,5-dihydroxy side chain has been a subject of several publications, for example
-
and references therein
-
Stereospecific synthesis of the 3,5-dihydroxy side chain has been a subject of several publications, for example, Heathcock, C. H., Rosen, T. Tetrahedron 1986, 42 (18), 4909 and references therein.
-
(1986)
Tetrahedron
, vol.42
, Issue.18
, pp. 4909
-
-
Heathcock, C.H.1
Rosen, T.2
-
12
-
-
85022970716
-
Synthesis of 6 is described in Scheme I
-
Synthesis of 6 is described in Scheme I.
-
-
-
-
13
-
-
0022486908
-
-
Hoffman, W. F.; Alberts, A. W.; Anderson, P. S.; Chen, J. S.; Smith, R. L.; Willard, A. K. J. Med. Chem. 1986, 29, 849.
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Willard, A.K.6
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14
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0022512448
-
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Stokker, G. E.; Alberts, A. W.; Gilfillan, J. L.; Huff, J. W.; Smith, R. L. J. Med. Chem. 1986, 29, 852.
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-
15
-
-
0022648502
-
-
Stokker, G. E.; Alberts, A. W.; Anderson, P. S.; Cragoe, E. J., Jr.; Deana, A. A.; Gilfillan, J. L.; Hirshfield, J.; Holtz, W. J.; Hoffman, W. F.; Huff, J. W.; Lee, T. J.; Novello, F. C.; Prugh, J. D.; Rooney, C. S.; Smith, R. L.; Willard, A. K. J. Med. Chem. 1986, 29, 170.
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Novello, F.C.12
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Smith, R.L.15
Willard, A.K.16
-
16
-
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0021997673
-
-
Stokker, G. E.; Hoffman, W. F.; Alberts, A. W.; Cragoe, E. J., Jr.; Deana, A. A.; Gilfillan, J. L.; Huff, J. W.; Novello, F. C.; Prugh, J. D.; Smith, R. L.; Willard, A. K. J. Med. Chem. 1985, 28, 347.
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Huff, J.W.7
Novello, F.C.8
Prugh, J.D.9
Smith, R.L.10
Willard, A.K.11
-
17
-
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0022643559
-
-
Hoffman, W. F.; Alberts, A. W.; Cragoe, E. J., Jr.; Deana, A. A.; Evans, B. E.; Gilfillan, N. P.; Gould, J. L.; Huff, J. W.; Novello, F. C.; Prugh, J. D.; Rittle, K. E.; Smith, R. L.; Willard, A. K. J. Med. Chem. 1986, 29,159.
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Gould, J.L.7
Huff, J.W.8
Novello, F.C.9
Prugh, J.D.10
Rittle, K.E.11
Smith, R.L.12
Willard, A.K.13
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22
-
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0023845547
-
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Boader, E.; Baitmann, W.; Beck, G.; Bergmann, A.; Jendialla, H.; Kessler, K.; Wess, G.; Schnbert, W.; Granzer, E.; Kerekjarto, B. V.; Krause, R. Tetrahedron Lett. 1988, 29 (8), 929.
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84982064797
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0019236427
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Medicinal Chemistry of Tetrazoles
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85022622903
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0001755803
-
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Wiley: New York Collect.
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-
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Prout, F.S.1
-
30
-
-
85022925018
-
Rate of condensation was observed to be slow and was further retarded if higher boiling solvents (such as toluene, xylenes, ethylbenzene) were used
-
but a similar period of time was needed to achieve the stated yields
-
Rate of condensation was observed to be slow and was further retarded if higher boiling solvents (such as toluene, xylenes, ethylbenzene) were used. Large excess of ethyl cyanoacetate could speed up the reaction, but a similar period of time was needed to achieve the stated yields.
-
Large excess of ethyl cyanoacetate could speed up the reaction
-
-
-
31
-
-
85022919322
-
The strongly electron deficient olefin 5 can also be cleaved by primary amines such as 2,2-dimethoxyethylamine to give the following imine
-
The strongly electron deficient olefin 5 can also be cleaved by primary amines such as 2,2-dimethoxyethylamine to give the following imine.
-
-
-
-
32
-
-
85022925395
-
-
Los Angeles, CA, September MEDI 109
-
Balasubramanian, N.; Brown, P. J.; Catt, J. D.; Han, W. T.; Sit, S. Y.; Wright, J. J. 196th National Meeting of the American Chemical Society, Los Angeles, CA, September 26–30, 1988. MEDI 109.
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(1988)
196th National Meeting of the American Chemical Society
, pp. 26-30
-
-
Balasubramanian, N.1
Brown, P.J.2
Catt, J.D.3
Han, W.T.4
Sit, S.Y.5
Wright, J.J.6
-
34
-
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84987466985
-
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Kathawala, F. G.; Prager, B.; Prassad, K.; Repic, O.; Shapiro, M. J.; Stabler, R. S.; Widler, L. Helv. Chim. Acta 1986, 69, 803.
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Stabler, R.S.6
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-
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-
38
-
-
85022972304
-
The changes in the product ratio may be attributed to the intramolecular chelation of the countercation to the ester carbonyl group
-
The changes in the product ratio may be attributed to the intramolecular chelation of the countercation to the ester carbonyl group.
-
-
-
-
40
-
-
84942707172
-
1,5-Dimethyltetrazole was once commercially available from Aldrich Chemicals and is still commercially available from Dynamite Nobel on a custom-order basis
-
1,5-Dimethyltetrazole was once commercially available from Aldrich Chemicals and is still commercially available from Dynamite Nobel on a custom-order basis. Preparation: Condon, F. E.; Walfmann, R.; Kundu, N.; Trivedi, J. P. Org. Prep. Proc. 1974, 6 (3), 135.
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Condon, F.E.1
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-
41
-
-
85022984966
-
The primary purpose of performing this experiment was to establish the regiochemistry of 18a and 18b. In practice, a single fractional crystallization of the methylation crude product could provide over 50% yield of the desired product 18a
-
The primary purpose of performing this experiment was to establish the regiochemistry of 18a and 18b. In practice, a single fractional crystallization of the methylation crude product could provide over 50% yield of the desired product 18a.
-
-
-
-
43
-
-
85022974142
-
Product was contaminated by a small amount (2-4%) of 1-methyl-5-isopropyltetrazole arising from the bis-alkylation
-
Product was contaminated by a small amount (2-4%) of 1-methyl-5-isopropyltetrazole arising from the bis-alkylation.
-
-
-
-
44
-
-
85022932576
-
The versatile bromide 29 was also oxidized by 2-nitropropane (EtONa) to furnish over 95% of aldehyde 20a. This intermediate is useful for analogue synthesis
-
The versatile bromide 29 was also oxidized by 2-nitropropane (EtONa) to furnish over 95% of aldehyde 20a. This intermediate is useful for analogue synthesis.
-
-
-
-
47
-
-
85022920008
-
The lithium carboxylate salt (generated by adding a molar equivalent of n-BuLi into the free acid) was used in the coupling with the anion of phosphonate ester
-
The lithium carboxylate salt (generated by adding a molar equivalent of n-BuLi into the free acid) was used in the coupling with the anion of phosphonate ester.
-
-
-
-
48
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85022607862
-
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Being less relevant in the present context, these results are not reported here
-
Being less relevant in the present context, these results are not reported here.
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Naylor, C.B.3
Mayer, D.4
Dammkoehler, E.A.5
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79
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Motoc, I.; Marshall, G. R.; Labanowski, J. Z. Naturforsch. 1985, 40a, 1121.
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(1985)
Z. Naturforsch.
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, pp. 1121
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Motoc, I.1
Marshall, G.R.2
Labanowski, J.Z.3
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80
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0346165766
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Motoc, I.; Marshall, G. R.; Dammkoehler, R. A.; Labanowski, J. Naturforsch. 1985, 40a, 1108.
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(1985)
Naturforsch.
, vol.40a
, pp. 1108
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Motoc, I.1
Marshall, G.R.2
Dammkoehler, R.A.3
Labanowski, J.4
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84
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0007581116
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For recent reviews
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Burgen, A. S. V., Roberts, G. C. K., Tute, M. S., Eds.; Elsevier: Amsterdam Chapter 5
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For recent reviews: Marshall, G. R.; Motoc, I. In Molecular Graphics and Drug Design; Burgen, A. S. V., Roberts, G. C. K., Tute, M. S., Eds.; Elsevier: Amsterdam, 1986; Chapter 5.
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(1986)
Molecular Graphics and Drug Design
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Marshall, G.R.1
Motoc, I.2
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86
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85022914951
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The values of the atomic van der Waals radius (rw, Å) used in calculations are: 1.08 (H), 1.53 (C), 1.48 (N), 1.65 (Cl), 1.30 (F), 1.75 (P), 1.72 (S)
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The values of the atomic van der Waals radius (rw, Å) used in calculations are: 1.08 (H), 1.53 (C), 1.48 (N), 1.65 (Cl), 1.30 (F), 1.75 (P), 1.72 (S).
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88
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0023751431
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For previous use of cross-validation in regression models
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For previous use of cross-validation in regression models, see: Cramer, R. D.; Patterson, D. E.; Bunce, F. D. J. Am. Chem. Soc. 1988, 110, 5959.
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(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 5959
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Cramer, R.D.1
Patterson, D.E.2
Bunce, F.D.3
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89
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0004107550
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3rd ed.; Allyn and Bacon: Boston
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Levine, I. N. Quantum Chemistry, 3rd ed.; Allyn and Bacon: Boston, 1986; p 481.
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(1986)
Quantum Chemistry
, pp. 481
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Levine, I.N.1
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90
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84987151416
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Baader, E.; Bartman, W.; Bergmann, A.; Lendralla, H.; Kes-seller, K.; Wess, G.; Schubert, W. Actual. Chim. Ther. 1989, 16, 133.
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(1989)
Actual. Chim. Ther.
, vol.16
, pp. 133
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Baader, E.1
Bartman, W.2
Bergmann, A.3
Lendralla, H.4
Kes-seller, K.5
Wess, G.6
Schubert, W.7
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91
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85022960032
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S0, and its square, S02, in molecular shape analysis studies in combination with other parameters (e.g., partition coefficients, length of substituent) and has further utilized the conformation corresponding to one of the energy minima of a selected compound of the series under consideration as reference structure
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Hopfinger54 has utilized the overlapping volume descriptor, S0, and its square, S02, in molecular shape analysis studies in combination with other parameters (e.g., partition coefficients, length of substituent) and has further utilized the conformation corresponding to one of the energy minima of a selected compound of the series under consideration as reference structure.
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Hopfinger54 has utilized the overlapping volume descriptor
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