Recherche de Sous-structure

51488

CC(=O)c1cc2ccccc2cn1
Reaction #1027
3-acetyl-isoquinoline
Rendement 14.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1nc(Cl)c2ccccc2c1-c1ccccc1
Reaction #75091
3-tert.butyl-1-chloro-4-phenyl isoquinoline
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C(=O)NCC(=O)O)nc(Cl)c2ccccc12
Reaction #173044
DOI: 10.1039/C8SC04228D
CCCCOC(=O)c1nc(C#N)c2ccc(Oc3c(C)cccc3CC)cc2c1O
Reaction #174612
DOI: 10.1039/C8SC04228D
CC(C)Oc1ccc2c(O)c(C(=O)NCCN(C)C)nc(Cl)c2c1
Reaction #175773
DOI: 10.1039/C8SC04228D
Cn1c(C=CC(=O)Cl)c(-c2ccccc2)c2ccccc2c1=O
Reaction #180823
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #182320
DOI: 10.1039/C8SC04228D
COc1ccc2cnc(C#N)c(-c3ccccc3F)c2c1
Reaction #185301
DOI: 10.1039/C8SC04228D
CC(NC(=O)c1nc(Br)c2ccccc2c1O)C(=O)O
Reaction #204663
DOI: 10.1039/C8SC04228D
CC(C)Oc1cccc(NC(=O)OCc2c(-c3ccccc3)c3cc(Cl)ccc3c(=O)n2C)c1
Reaction #205255
DOI: 10.1039/C8SC04228D
CNC(=O)N1CCC(Cn2c(C(=O)OC)c(-c3ccccc3)c3cc(Br)ccc3c2=O)CC1
Reaction #208128
DOI: 10.1039/C8SC04228D
COC(=O)C(Cc1ccc(OCc2ccccc2)cc1)NC(=O)c1cc2cc(Oc3ccc(C(C)(C)C)cc3)ccc2cn1
Reaction #213192
DOI: 10.1039/C8SC04228D
N#Cc1c(NCc2cc3ccccc3cn2)nc(N)nc1-n1cccn1
Reaction #222864
DOI: 10.1039/C8SC04228D
N=C(c1ccc(Cl)cc1)c1cc2ccccc2cn1
Reaction #226795
DOI: 10.1039/C8SC04228D
COC(=O)CC(=O)CC(O)C=Cc1c(-c2ccc(F)cc2)n(CCc2ccccc2)c(=O)c2ccccc12
Reaction #233151
DOI: 10.1039/C8SC04228D
COCCc1cc2ccccc2cn1
Reaction #234236
DOI: 10.1039/C8SC04228D
CCOC(=O)NCCc1cc2ccccc2cn1
Reaction #236188
DOI: 10.1039/C8SC04228D
O=c1[nH]c2c(c3ccccc13)Cc1cc(S(=O)(=O)Cl)ccc1-2
Reaction #236830
DOI: 10.1039/C8SC04228D
CCCCOC(=O)c1nc(SCC)c2ccccc2c1O
Reaction #237326
DOI: 10.1039/C8SC04228D
CC(C)Oc1ccc2c(O)c(C(=O)NCCO)nc(Cl)c2c1
Reaction #242604
DOI: 10.1039/C8SC04228D
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