Recherche de Sous-structure

788907

CCOC(=O)c1cc2c(Cl)ccc(Oc3ccc(N)cc3)c2n1C
Reaction #178739
DOI: 10.1039/C8SC04228D
CC1CNCc2cc3ccc(C(F)(F)F)cc3n21
Reaction #179857
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(Cl)nc1)c1cc2ccc(C(F)(F)F)nc2n1Cc1cccc(F)c1
Reaction #185327
DOI: 10.1039/C8SC04228D
Cc1cc(Cc2ccc(NS(C)(=O)=O)cc2F)n(C)c1C(=O)c1ccccc1
Reaction #188482
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc2cc([N+](=O)[O-])ccc2n1Cc1ccc(F)cc1F
Reaction #195094
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc2c(C)ccc([N+](=O)[O-])c2n1COC
Reaction #198168
DOI: 10.1039/C8SC04228D
CC(C)N1CCC(Oc2ccc3c(c2)cc2n3C(CO)CN(C)C2=O)CC1
Reaction #201018
DOI: 10.1039/C8SC04228D
Nc1cc(NC(=O)c2cc3cc(C(F)(F)F)cnc3n2Cc2cccc(F)c2)ccn1
Reaction #203793
DOI: 10.1039/C8SC04228D
CCn1c(C(=O)N(C2CC2)C2CC2)cc2c3c(ncn3C)c(Nc3cc(C)n(C)n3)nc21
Reaction #204686
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(-c2ccc(-c3ccccc3CO)cc2)c(C#N)cn1C
Reaction #210257
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)n1c(C(=O)N2CCOCC2)cc2cc(OC3CCN(C4CC4)CC3)cnc21
Reaction #212509
DOI: 10.1039/C8SC04228D
COC(=O)c1c(-c2ccccc2Cl)c2cc(C)cc(C)c2n1C
Reaction #216052
methyl 3-(2-chlorophenyl)-1,5,7-trimethylindole-2-carboxylate
Rendement 58.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(Cc1ccc2c(c1)cc(C(=O)OCc1ccccc1)n2Cc1ccc([N+](=O)[O-])cc1)NCC(O)COc1ccccc1
Reaction #221147
DOI: 10.1039/C8SC04228D
COC(=O)c1cc2cc(CBr)cc([N+](=O)[O-])c2n1C(=O)OC(C)(C)C
Reaction #224811
DOI: 10.1039/C8SC04228D
COC(=O)c1cccc(-n2c(C(=O)OC)c(CCSC(C)=O)c3ccccc32)c1
Reaction #229832
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(Cc2cccc3ccccc23)c2ccccc2n1CCOC
Reaction #233900
DOI: 10.1039/C8SC04228D
Cc1c2c(c(C(=O)O)n1-c1ccccc1)C(C)(C#N)CC2(C)C
Reaction #235968
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc2c(n1CCN)CCCC2
Reaction #240634
DOI: 10.1039/C8SC04228D
COC(=O)c1c(Oc2ccccc2[N+](=O)[O-])c2ccccc2n1C
Reaction #241265
DOI: 10.1039/C8SC04228D
CCN1CCn2c(cc3cc(OC4CCN(C(C)C)CC4)ccc32)C1=O
Reaction #242992
DOI: 10.1039/C8SC04228D
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