Teilstruktursuche

73193

CC(=O)Nc1ccc2c3c(cccc13)CC2
Reaction #2047
5-(N-acetylamino)acenaphthene
Ausbeute 96.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Nc2ccc3c4c(cccc24)CC3)cc1
Reaction #2048
5-[N-(4-tolyl)amino]acenaphthene
Ausbeute 72.3%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #50689
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #50690
title compound
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2c(c1)ccc1ccccc12
Reaction #50908
phenanthrene
Ausbeute 131.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2c(Cl)ccc3ccccc23)[n+]([O-])c1
Reaction #158000
2-(2-chloronaphthalen-1-yl)-5-methylpyridine-1-oxide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(C=O)c(-c3ccc(F)cc3F)ccc2c1
Reaction #183399
DOI: 10.1039/C8SC04228D
N#Cc1ccc(N2CCC(=NO)C2)c2ccccc12
Reaction #185377
DOI: 10.1039/C8SC04228D
COC(=O)CC(=O)CC(O)CCc1c(C)cc(Cl)c2ccc(Cl)cc12
Reaction #189038
DOI: 10.1039/C8SC04228D
CC1CCCCN1c1ccc(C#N)c2ccccc12
Reaction #193543
DOI: 10.1039/C8SC04228D
COc1ccc(C2=Cc3ccc4ccccc4c3C2)cc1
Reaction #194149
DOI: 10.1039/C8SC04228D
Cc1ccc2ccccc2c1-c1c(C)ccc2ccccc12
Reaction #196206
DOI: 10.1039/C8SC04228D
Cc1cc(Cl)c2ccc(Cl)cc2c1CCC=O
Reaction #197405
DOI: 10.1039/C8SC04228D
CC1=Cc2c(cccc2-c2cccc3ccccc23)C1
Reaction #199024
DOI: 10.1039/C8SC04228D
CC(C)c1cccc(C(C)C)c1N=Cc1cccc(-c2c(CNC(C)(C)C)ccc3ccccc23)n1
Reaction #201181
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C)(C)Oc1n[nH]c(C)c1-c1cccc2ccccc12
Reaction #209473
DOI: 10.1039/C8SC04228D
FC(F)(F)c1ccc(N2CCCCC2)c2ccccc12
Reaction #213491
DOI: 10.1039/C8SC04228D
COc1ccc2cccc(C=CN3C(=O)c4ccccc4C3=O)c2c1
Reaction #234119
DOI: 10.1039/C8SC04228D
CC1CN(c2ccc3c4c(cccc24)CC3)CCN1CCC1OCCc2cc(N3CCCS3(=O)=O)ccc21
Reaction #241175
DOI: 10.1039/C8SC04228D
N#Cc1ccc(N2C3CCC2CC(NC(=O)CCn2ccnc2)C3)c2ccccc12
Reaction #254210
DOI: 10.1039/C8SC04228D
Seite 1Weiter