#2585

Cc1nn(C)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(C#N)cn1
Reaction #132
Ausbeute 54.9%750 AstraZeneca ELN dataset
Clc1ccnc(Nc2ncco2)c1
Reaction #415
Ausbeute 0.5%750 AstraZeneca ELN dataset
Clc1ccnc(Nc2ncco2)c1
Reaction #459
Ausbeute 3.0%750 AstraZeneca ELN dataset
Clc1ccnc(Nc2ncco2)c1
Reaction #462
Ausbeute 2.5%750 AstraZeneca ELN dataset
N#Cc1cccc(Oc2ccccc2)c1C#N
Reaction #2727
1,2-dicyano-3-phenoxybenzene
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1ccc(Oc2ccccc2)cc1C#N
Reaction #2728
1,2-Dicyano-4-phenoxybenzene
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1c(-c2ccc(F)cc2)c(-c2ccnc(Oc3ccccc3)n2)n2n1CC(O)C2
Reaction #7756
desired product
Ausbeute 21.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
[O-]c1ccccc1
Reaction #42696
phenoxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=CC(Oc1ccccc1)c1ccccc1
Reaction #42718
1-phenyl-1-phenoxy-2-propene
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=CC(Oc1ccccc1)c1ccccc1
Reaction #42719
title compound
Ausbeute 81.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=c1c(-c2ccc(F)cc2)c(-c2ccnc(Oc3ccccc3)n2)n2n1CC(O)C2
Reaction #50964
desired product
Ausbeute 21.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(Cl)c(Oc2c(COc3ccccc3)nc(N3CCOCC3)nc2NS(=O)(=O)c2ccc(C(C)(C)C)cc2)c1
Reaction #65380
4-tert.-butyl-N-[5-(2-chloro-5-methoxy-phenoxy)-2-morpholin-4-yl-6-phenoxymethyl-pyrimidin-4-yl]benzenesulphonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(C=NO)Oc1ccccc1
Reaction #93765
α-phenoxy propionaldehyde oxime
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
Clc1nccnc1Oc1ccccc1
Reaction #95012
2-chloro-3-phenoxypyrazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
Nc1ncc(Oc2ccccc2)nc1N1CCOCC1
Reaction #95036
2-amino-3-morpholino-5-phenoxypyrazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
Nc1nnc2ccc(Oc3ccccc3)nn12
Reaction #304854
title compound
Ausbeute 20.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CCCC[N+](CCCC)(CCCC)CCCC.O=S(=O)([O-])CCCCOc1ccccc1
Reaction #326379
tetrabutylammonium 4-phenoxybutylsulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
C=CCCC(=O)Oc1ccccc1
Reaction #327417
ester
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CN(C)c1cc(-c2ccccc2)[n+](C)n1C.[I-]
Reaction #354537
1,2-Dimethyl-3-dimethylamino-5-phenylpyrazolium Iodide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1976_03
Clc1nccnc1Oc1ccccc1
Reaction #355115
2-chloro-3-phenoxypyrazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1976_03
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