Ähnlichkeitssuche

1069213

COC(=O)Cc1ccc(Nc2ncc3cc(-c4c(Cl)cccc4Cl)c(=O)n(C)c3n2)cc1
Reaction #3309
{4-[6-(2,6-Dichlorophenyl)-8-methyl-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidin-2-ylamino]phenyl}-acetic acid, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Br)c1ccccc1
Reaction #4069
title compound
Ausbeute 93.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(c1ccc(F)cc1)C(O)c1ccnc(SC)n1
Reaction #7732
desired product
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C(=O)OC)c1ccc(Cl)cc1
Reaction #8706
2-(4-chloro-phenyl)-malonic acid dimethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1ccc(OC(C)C)cc1
Reaction #9347
methyl (4-(1-methylethoxy)phenyl)acetate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1)NO
Reaction #10026
N-hydroxy-2-phenylacetamide
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1cnc(Cl)nc1Cl)c1ccc(OC)cc1
Reaction #11858
3-(2,4-dichloro-pyrimidin-5-yl)-2-(4-methoxy-phenyl)-propionic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1cnc(Cl)nc1Cl)c1ccccc1
Reaction #11868
3-(2,4-dichloro-pyrimidin-5-yl)-2-phenyl-propionic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1ccc(Cl)cc1
Reaction #40576
methyl 2-(4-chlorophenyl)acetate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1ccc(I)cc1
Reaction #42728
title compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CC#N)c1ccc(Cl)cc1
Reaction #51209
title product
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1ccc(C#Cc2ccc3c(c2)C(C)(C)CN(C2CC2)C3)cc1
Reaction #52360
title compound
Ausbeute 23.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1ccc(C#Cc2ccc3c(c2)C(C)(C)CC(C)(C)O3)cc1
Reaction #52364
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1ccc(C#Cc2cc(C3CC3)c3c(c2)C(C)(C)CC(C)(C)O3)cc1
Reaction #52380
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(C#Cc2ccc(CC(=O)OC)cc2)cc2c1OC(C)(C)CC2(C)C
Reaction #52400
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1ccc(C#Cc2ccc3c(c2)C(C)(C)CCN3C2CC2)cc1
Reaction #52411
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1ccc(C#Cc2ccc(C3(OC)CC3)cc2)cc1
Reaction #52418
title compound
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1ccc(C#Cc2ccc(C3(OC(C)C)CC3)cc2)cc1
Reaction #52425
title compound
Ausbeute 70.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1ccc(C#Cc2ccc(C3(OCc4ccccc4)CC3)cc2)cc1
Reaction #52431
title compound
Ausbeute 161.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1ccc(C#Cc2ccc(C3(OCc4ccccc4)CC3)c(C)c2)cc1
Reaction #52438
title compound
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
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