-
1
-
-
0001891550
-
A rhodium-induced cyclization-cycloaddition sequence for the construction of conformationally rigid calcium channel modulators of the dihydropyrimidine type
-
Synthesis and Reactions of Biginelli Compounds, Part 15; for Part 14, see: Jauk B, Belaj F, Kappe CO. A rhodium-induced cyclization-cycloaddition sequence for the construction of conformationally rigid calcium channel modulators of the dihydropyrimidine type. J Chem Soc, Perkin Trans 1 1999;307-314.
-
(1999)
J Chem Soc, Perkin Trans 1
, vol.1
, pp. 307-314
-
-
Jauk, B.1
Belaj, F.2
Kappe, C.O.3
-
2
-
-
0027205552
-
100 years of the Biginelli Dihydropyrimidine synthesis
-
Review: Kappe CO. 100 Years of the Biginelli Dihydropyrimidine Synthesis. Tetrahedron 1993;49:6937-6963.
-
(1993)
Tetrahedron
, vol.49
, pp. 6937-6963
-
-
Kappe, C.O.1
-
3
-
-
0025105557
-
3-substituted-4-aryl-1,4-dihydro-6-methyl-5-pyrimidinecarboxylic acid esters as potent mimics of dihydropyridines
-
Atwal KS, Rovnyak GC, Kimball SD, Floyd DM, Moreland S, Swanson BN, Gougoutas JZ, Schwartz J, Smillie KM, Malley MF. 3-Substituted-4-aryl-1,4-dihydro-6-methyl-5-pyrimidinecarboxylic acid esters as potent mimics of dihydropyridines. J Med Chem 1990;33:2629-2635.
-
(1990)
J Med Chem
, vol.33
, pp. 2629-2635
-
-
Atwal, K.S.1
Rovnyak, G.C.2
Kimball, S.D.3
Floyd, D.M.4
Moreland, S.5
Swanson, B.N.6
Gougoutas, J.Z.7
Schwartz, J.8
Smillie, K.M.9
Malley, M.F.10
-
4
-
-
0026065919
-
3-carbamoyl-4-aryl-1,2,3,4-tetrahydro-6-methyl-5-pyrimidinecarboxylic acid esters as orally effective antihypertensive agents
-
Atwal KS, Swanson BN, Unger SE, Floyd DM, Moreland S, Hedberg A, O'Reilly BC. 3-Carbamoyl-4-aryl-1,2,3,4-tetrahydro-6-methyl-5-pyrimidinecarboxylic acid esters as orally effective antihypertensive agents. J Med Chem 1991;34:806-811.
-
(1991)
J Med Chem
, vol.34
, pp. 806-811
-
-
Atwal, K.S.1
Swanson, B.N.2
Unger, S.E.3
Floyd, D.M.4
Moreland, S.5
Hedberg, A.6
O'Reilly, B.C.7
-
5
-
-
0026759681
-
Basic 3-substituted-4-aryl-1,4-dihydropyrimidine-5-carboxylic acid esters. Potent antihypertensive agents
-
Rovnyak GC, Atwal KS, Hedberg A, Kimball SD, Moreland S, Gougoutas JZ, O'Reilly BC, Schwartz J, Malley MF. Basic 3-substituted-4-aryl-1,4-dihydropyrimidine-5-carboxylic acid esters. Potent antihypertensive agents. J Med Chem 1992;35:3254-3263.
-
(1992)
J Med Chem
, vol.35
, pp. 3254-3263
-
-
Rovnyak, G.C.1
Atwal, K.S.2
Hedberg, A.3
Kimball, S.D.4
Moreland, S.5
Gougoutas, J.Z.6
O'Reilly, B.C.7
Schwartz, J.8
Malley, M.F.9
-
6
-
-
0029095690
-
Pharmacologic profile of the dihydropyrimidine calcium channel blockers SQ 32,547 and SQ 32,926
-
Grover GJ, Dzwonczyk S, McMullen DM, Normadinam CS, Sleph PG, Moreland S. Pharmacologic profile of the dihydropyrimidine calcium channel blockers SQ 32,547 and SQ 32,926. J Cardiovasc Pharmacol 1995;26:289-294.
-
(1995)
J Cardiovasc Pharmacol
, vol.26
, pp. 289-294
-
-
Grover, G.J.1
Dzwonczyk, S.2
McMullen, D.M.3
Normadinam, C.S.4
Sleph, P.G.5
Moreland, S.6
-
7
-
-
0029036894
-
Calcium channel blockers and activators: Conformational and structural determinants of dihydropyrimidine calcium channel modulators
-
Rovnyak GC, Kimball SD, Beyer B, Cucinotta G, DiMarco JD, Gougoutas J, Hedberg A, Malley M, McCarthy JP, Zhang R, Moreland S. Calcium channel blockers and activators: Conformational and structural determinants of dihydropyrimidine calcium channel modulators. J Med Chem 1995;38:119-129.
-
(1995)
J Med Chem
, vol.38
, pp. 119-129
-
-
Rovnyak, G.C.1
Kimball, S.D.2
Beyer, B.3
Cucinotta, G.4
DiMarco, J.D.5
Gougoutas, J.6
Hedberg, A.7
Malley, M.8
McCarthy, J.P.9
Zhang, R.10
Moreland, S.11
-
8
-
-
0026776479
-
Facile preparation and resolution of a stable dihydropyrimidinecarboxylic acid
-
Kappe CO, Uray G, Roschger P, Lindner W, Kratky C, Keller W. Facile preparation and resolution of a stable dihydropyrimidinecarboxylic acid. Tetrahedron 1992;48:5473-5480.
-
(1992)
Tetrahedron
, vol.48
, pp. 5473-5480
-
-
Kappe, C.O.1
Uray, G.2
Roschger, P.3
Lindner, W.4
Kratky, C.5
Keller, W.6
-
9
-
-
0031008496
-
Separation of enantiomers of 4-aryldihydropyrimidines by direct enantioselective HPLC. A critical comparison of chiral stationary phases
-
Kleidernigg OP, Kappe CO. Separation of enantiomers of 4-aryldihydropyrimidines by direct enantioselective HPLC. A critical comparison of chiral stationary phases. Tetrahedron: Asymmetry 1997;8:2057-2067.
-
(1997)
Tetrahedron: Asymmetry
, vol.8
, pp. 2057-2067
-
-
Kleidernigg, O.P.1
Kappe, C.O.2
-
10
-
-
0001858454
-
Highly selective chiral recognition on polymer supports: Preparation of a combinatorial library of dihydropyrimidines and its screening for novel chiral HPLC ligands
-
Lewandowski K, Murer P, Svec F, Fréchet JMJ. Highly selective chiral recognition on polymer supports: Preparation of a combinatorial library of dihydropyrimidines and its screening for novel chiral HPLC ligands, Chem Commun 1998;2237-2238.
-
(1998)
Chem Commun
, pp. 2237-2238
-
-
Lewandowski, K.1
Murer, P.2
Svec, F.3
Fréchet, J.M.J.4
-
11
-
-
0001125059
-
On-line measurement of circular dichroism spectra Δε(λ) during stops of chromatographic flow
-
Brandl G, Kastner F, Fritsch R, Zinner H, Mannschreck A On-line measurement of circular dichroism spectra Δε(λ) during stops of chromatographic flow. Monatsh Chem 1992;123:1059-1069.
-
(1992)
Monatsh Chem
, vol.123
, pp. 1059-1069
-
-
Brandl, G.1
Kastner, F.2
Fritsch, R.3
Zinner, H.4
Mannschreck, A.5
-
12
-
-
0027159124
-
Online measurement of circular-dichroism spectra during enantioselective liquid-chromatography
-
Mannschreck A Online measurement of circular-dichroism spectra during enantioselective liquid-chromatography. Trends Anal Chem 1993;12:220-225.
-
(1993)
Trends Anal Chem
, vol.12
, pp. 220-225
-
-
Mannschreck, A.1
-
13
-
-
26844487901
-
Polyphosphate ester-mediated synthesis of dihydropyrimidines. Improved conditions for the Biginelli reaction
-
Kappe CO, Falsone FS. Polyphosphate ester-mediated synthesis of dihydropyrimidines. Improved conditions for the Biginelli reaction. Synlett 1998;718-720.
-
(1998)
Synlett
, pp. 718-720
-
-
Kappe, C.O.1
Falsone, F.S.2
-
14
-
-
0003145860
-
Die allylgruppe als mild und selektiv abspalt-bare carboxy-schutzgruppe zur synthese empfindlicher O-glycopeptide
-
Kunz H, Waldmann H. Die Allylgruppe als mild und selektiv abspalt-bare Carboxy-Schutzgruppe zur Synthese empfindlicher O-Glycopeptide. Angew Chem 1984;96:49-50.
-
(1984)
Angew Chem
, vol.96
, pp. 49-50
-
-
Kunz, H.1
Waldmann, H.2
-
15
-
-
0030950586
-
Lipase-catalyzed enantioselective hydrolysis of bis(acyloxymethyl) 1,4-dihydro-3,5-pyridinecarboxylates leading to optically active medicines
-
Ebiike H, Maruyama K, Yamazaki Y, Hirose Y, Kariya K, Sasaki I, Kurono Y, Terao Y, Achiwa K. Lipase-catalyzed enantioselective hydrolysis of bis(acyloxymethyl) 1,4-dihydro-3,5-pyridinecarboxylates leading to optically active medicines. Chem Pharm Bull 1997;45:863-868.
-
(1997)
Chem Pharm Bull
, vol.45
, pp. 863-868
-
-
Ebiike, H.1
Maruyama, K.2
Yamazaki, Y.3
Hirose, Y.4
Kariya, K.5
Sasaki, I.6
Kurono, Y.7
Terao, Y.8
Achiwa, K.9
-
16
-
-
4644248683
-
Use of enzymes in the preparation of enantiopure 1,4-dihydropyridines
-
Marchalin S, Chudik M, Masthuba V, Decroix B. Use of enzymes in the preparation of enantiopure 1,4-dihydropyridines. Heterocycles 1998;48:1943-1958.
-
(1998)
Heterocycles
, vol.48
, pp. 1943-1958
-
-
Marchalin, S.1
Chudik, M.2
Masthuba, V.3
Decroix, B.4
-
17
-
-
0027897680
-
A simple method to determine the enantiomeric ratio in enantioselective biocatalysis
-
Rakels JLL, Straathof AJJ, Heijnen JJ. A simple method to determine the enantiomeric ratio in enantioselective biocatalysis. Enzyme Microb Technol 1993;15:1051-1056.
-
(1993)
Enzyme Microb Technol
, vol.15
, pp. 1051-1056
-
-
Rakels, J.L.L.1
Straathof, A.J.J.2
Heijnen, J.J.3
|