Phenyloxazoles and phenylthiazoles as benzamide bioisosteres: synthesis and dopamine receptor binding profiles
J Einsiedel, C Thomas, H Hübner, P Gmeiner
Index: Einsiedel, Juergen; Thomas, Christoph; Huebner, Harald; Gmeiner, Peter Bioorganic and Medicinal Chemistry Letters, 2000 , vol. 10, # 17 p. 2041 - 2044
Full Text: HTML
Citation Number: 31
Abstract
In order to recognize the essential structural features of the systems we were intrigued by the question whether oxazole or thiazole moieties could be employed as an alternative with substantially different electronic properties being, furthermore, devoid of a H-donating group. These deliberations led us to compounds of type 4 when we planned to incorporate N-phenylpiperazinylmethyl, N-benzylpiperazinylmethyl or N-benzylpiperidinylaminomethyl side chains. In order to ...
Related Articles:
The synthesis and activity of oxazole and thiazole analogues of urocanic acid
[Millan, David S.; Prager, Rolf H.; Brand, Catherine; Hart, Prue H. Tetrahedron, 2000 , vol. 56, # 5 p. 811 - 816]
[Bioorganic and Medicinal Chemistry Letters, , vol. 10, # 17 p. 2041 - 2044]
[Chemische Berichte, , vol. 101, # 11 p. 3872 - 3882]
[Archiv der Pharmazie, , vol. 343, # 7 p. 411 - 416]
[Chemische Berichte, , vol. 101, # 11 p. 3872 - 3882]