2.5 to 4.5 K
5 Methyl 2 (4 methylbenzoyloxy)acetophenone
8
trans 3 Acetyl 5 benzoyl 2 methyl 4 phenyl 4,5 dihydrofuran at 150 K
10
2 Amino 5 phenyl 1,3,4 thiadiazole at 110 K
6
4 {5 [3,4 Dimethyl 5 (3,4,5 trimethoxyphenyl)thiophen 2 yl] 2 methoxyphenyl}morpholine
9
2 Amino 5 chloropyridinium 4 aminobenzoate
7
(4R,5R) 2 (N Methyl benzylamino) 3 nitro 4 (1′,2′,3′,4′,5′ penta O acetyl D manno pentitol 1 yl) 5 phenyl 5 phenylcarbamoyl 4,5 dihydrothiophene at 150 K
11
4-Ammonio-5-methoxy-2-methylbenzenesulfonate
6
5 (4 Methoxyphenyl) 4 methyl 2 thioxo 2,3 dihydro 1,3 thiazol 3 yl benzoate at 100 K
8
5 Bromo 2 chloropyrimidin 4 amine
6
4 (4 Bromo 5 methylthiophen 2 yl)pyridine
5
5 Formyl 2 furanboronic acid at 100 K
8
4 (4 Bromophenylhydrazono) 1 (5 bromopyrimidin 2 yl) 3 methyl 2 pyrazolin 5 one
13
4 Hydroxy 5 (4 methoxyphenyl)pyrrolidin 2 one
8
5 (4 Methoxyphenyl) 4 methylthiazole 2(3H) thione
7
5 Isopropyl 5 methyl 2 sulfanylideneimidazolidin 4 one
7
An econometric analysis of the Australian Country Party, 1922-1928
209
5��4���D�6� 5��� ������6� 5� ����6�
6
SYNTHESIS OF 1 SUBSTITUTED 2 [2 (4, 5/5, 6/5, 7 DIMETHYL) 2 OXOINDOLIN 3 YLIDENE) HYDRAZINYL] 3 PHENYLQUINAZOLIN 4(3H) ONES AS ANTIFUNGAL AGENTS
8
(±) 5 Ethyl 2 (4 isopropyl 4 methyl 5 oxo 4,5 dihydro 1H imidazol 2 yl)nicotinic acid
7
2 Amino 5 methylpyridinium 4 chlorobenzoate
9