2.5 to 3.6 V
1 Ethyl 3 (4 hydroxy 3 methoxyphenyl) 6 methoxy 2 methylindan 5 ol
11
An Efficient and Facile Synthesis of 4 Aryl 2 Hydroxy 6 {[(3′ Difluoromethoxy) 5′ (3″ Methyl) 4″ (2‴, 2‴, 2‴ Trifluoroethoxy) Pyridin 2″ Yl] Methoxyphenyl} 1 6 Dihy Dropyrimidines
6
2 (6 Fluoro 5 hydroxy 2 methyl 1H 3 indenyl)acetic acid
6
Green Synthesis of Novel 5 Arylazo 2 [(2S, 3S, 4R, 5R) 3, 4, 5 Trihydroxy 6 (Hydroxymethyl) Tetrahydro 2H Pyran 2 Yloxy] 4, 6 Dimethyl 3 Nicotinonitrile
14
Methyl 5 hydroxy 2 (2 hydroxy 6 methoxy 4 methylbenzoyl) 3 methoxybenzoate
8
1′ Methyl 5′ phenyl 2′',3′',5′',6′′ tetrahydroindoline 3 spiro 3′ pyrrolidine 4′ spiro 2′' imidazo[2,1 b]thiazole 2,3′' dione
10
Diorthobenzenotetra(5′,2′ tetrazolo)[5′ (2) 2′ (6)]cyclophane
9
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
Synthesis and pharmacological screening of 5-methyl-3-[ P -(6'-aryl-2'-thioxo-1',2',5',6'-tetrahydro-pyrimidin-4'-yl)-phenyl]-3 H -2-oxo-D4-1,3,4-oxadiazoles
5
1 Methyl spiro[2 3′]oxindole spiro[3 2′′]5′′,6′′ dihydroimidazo[2′′,1′′ b]thiazol 3′′ one 4 (2 benzo[1,3]dioxol 5 yl)pyrrolidine
8
Complete V.6 No.2
394
SYNTHESIS AND ANTIFUNGAL ACTIVITY OF 1 SUBSTITUTED 3 (2 (6 CHLOROBENZOTHIAZOL 2 YL) HYDRAZONO) 4, 5/5, 6/5, 7 DIMETHYLINDOLIN 2 ONES
8
3 Benzylidene 3′,7′ diphenylcyclohexanespiro 6′ (perhydro 2 thiapyrrolizidine) 5′ spiro 3′′ 1H indole 2,2′′ dione
11
5 (2 Chlorobenzyl) 2 (2 hydroxyethyl) 6 methylpyridazin 3(2H) one
8
[1]; [2]; [3]; [4]; [5]; [6]; [7] . In regards to this, the
5
2′ (2 Chlorophenyl) 1′ nitro 2′,3′,4′,5′,6′,7′ hexahydro 1H indole 3 spiro 3′ 1′H pyrrolizin 2(3H) one
11
1′,5 Dinitro 2′ phenyl 2′,3′,5′,6′,7′,7a' hexahydrospiro[indoline 3,3′ 1′H pyrrolizin] 2 one
9
The implementation of OLASS: an assessment of its impact one year on
74
exo 7 Phenyl 3 n propyl 5 oxa 2 thia 6 azabicyclo[3 2 01,4]hept 6 ene 2,2 dioxide
7
Python Docs 2 5 2 (6) pdf
990