Teilstruktursuche

COC(=O)C(C)=O

CCOC(=O)C(=O)C(Cc1cc(OC)ccc1Br)C(=O)OCC
Reaction #5440
desired product
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)C(CCc1cc(OC)ccc1Br)C(=O)OCC
Reaction #5449
desired product
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)C(NC(=O)C1CCC1)c1cccc(OCc2ccccc2)c1
Reaction #46253
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)C1Cc1n[nH]c(=S)[nH]c1=O
Reaction #46259
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C(=O)Oc1c(C)cc(Nc2ccn(-c3ccccc3)n2)cc1C
Reaction #50556
2,6-Dimethyl-4-(1-phenyl-1H-pyrazol-3-yl)aminophenyl 2-oxopropanoate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccc(C(F)(F)CCC(=O)O)cc2)cc1
Reaction #52035
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)c1cc(Cl)c(C2CCCCC2)c(Cl)c1
Reaction #54824
ethyl 3,5-dichloro-4-cyclohexylphenylglyoxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc2ccccc2n1
Reaction #80821
2-acetylquinoline
Ausbeute 96.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)c1cc(Cl)cc2cccnc12
Reaction #94875
title product
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C(=O)OCC)c1cccc(Cl)c1
Reaction #173430
DOI: 10.1039/C8SC04228D
COC(=O)C1CCC2(CCN(C(=O)N(C)C(C)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)C(c3ccc(F)cc3C)C2)N1
Reaction #174113
DOI: 10.1039/C8SC04228D
COC(=O)C(=O)C(Cl)c1ccc(F)c(F)c1
Reaction #176765
DOI: 10.1039/C8SC04228D
CCOC(=O)C(=O)c1cc(F)cc2ccoc12
Reaction #177492
DOI: 10.1039/C8SC04228D
CCOC(=O)C(=O)c1ccc(SC2CC2)c(Br)c1
Reaction #178453
DOI: 10.1039/C8SC04228D
CCOC(=O)C(=O)CC(C)(C)c1cccc(C)c1OC
Reaction #183737
DOI: 10.1039/C8SC04228D
CCOC(=O)CC(=O)C(CC(C)C)C(=O)OCC
Reaction #194446
DOI: 10.1039/C8SC04228D
CCOC(=O)C(O)(CC1(c2cccc(F)c2OC)CC1)C(F)(F)F
Reaction #195661
DOI: 10.1039/C8SC04228D
CCOC(=O)C(=O)C(=NO)C(=O)c1c(Cl)cccc1Cl
Reaction #199242
DOI: 10.1039/C8SC04228D
O=C(O)C(=O)c1ccc(OCCCn2c(=O)ccc3ccccc32)cc1
Reaction #202029
DOI: 10.1039/C8SC04228D
C=C(C(=O)OC)c1cc2c(cc1OC)CCC(=O)N2C
Reaction #206589
DOI: 10.1039/C8SC04228D
Seite 1Weiter