1.6 to 5 s
(3aS,4S,5R,7aS,1′R,2a′S,6′S,6a′S) 5 (2′,5′ Dioxo 2a′ methyl 6′,6a′ epoxyperhydroinden 1′ yl) 3a,4 epoxy 5 hydroxy 7a methylperhydro 1H inden 1 one
7
Crystal structures of 4 phenylpiperazin 1 ium 6 chloro 5 ethyl 2,4 dioxopyrimidin 1 ide and 4 phenylpiperazin 1 ium 6 chloro 5 isopropyl 2,4 dioxopyrimidin 1 ide
17
On AdS(5) x S**5 String S matrix
11
The 1:1 adduct of antimony trifluoride with [1 5]dibenzothia 18 crown 6
9
(2S,3a'R,4′R,5′S,6′R) 4′,5′ Isoprolidenedioxy 6′ (trityloxymethyl) 2′ oxotetrahydro 1H spiro[pyrrolidine 2,3′ pyrrolo[1,2 b]isoxazole] 1 carbaldehyde
10
1 (5 Chloro 6 methoxynaphthalen 2 yl)propan 1 one
6
Methyl 8 hydroxy (S) 3 methyl 1 oxoisochromane 5 carboxylate (5 methoxycarbonylmellein)
8
1(5),6(7) Diepoxy 4 guaiol hemihydrate
13
5 Amino 6 methylquinolin 1 ium 3 carboxypropanoate
11
A 0 5 V, 1 2 GS/s, 6 Bit Flash ADC Using Temporarily Boosted Comparator
9
Kerklike tug volgens 1 Korintiërs 5 en 6
14
[1]; [2]; [3]; [4]; [5]; [6]; [7] . In regards to this, the
5
3 (4 Bromophenyl) 3 (4 hydroxy 6 oxo 1,6 dihydropyrimidin 5 yl) N [(S) 1 phenylethyl]propanamide
8
6. S. Jadhao and A. S. Bhuktar
10
2,2′,5′,6 Tetrachloro 4 [(1S) 1 methylpropoxy]biphenyl
7
1 Methoxymethyl 5 ethyl 6 (1 naphthylmethyl)uracil
10
SYNTHESIS AND ANTIFUNGAL ACTIVITY OF 1 SUBSTITUTED 3 (2 (6 CHLOROBENZOTHIAZOL 2 YL) HYDRAZONO) 4, 5/5, 6/5, 7 DIMETHYLINDOLIN 2 ONES
8
(2′′S,5′′R,7′′S) 2 [2′ (2′′ Methyl 1′′,6′′ dioxaspiro[4 5]dec 7′′ yl)ethylsulfonyl] 1,3 benzothiazole
7
Drie nuwe verklaringsopsies in die Jakobusbrief (Jak 2:1; 4:5; 5:6)
15
6(S) Methyl 3(S) (1 methylethyl)piperazin 2 one
9