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32966

O=C(CBr)Nc1cccc(-c2cnc3ccccc3n2)c1
Reaction #226869
DOI: 10.1039/C8SC04228D
C=CC(=O)Nc1cccc(-c2cnc3ccccc3n2)c1
Reaction #233430
DOI: 10.1039/C8SC04228D
COc1ccc(CN2Cc3c(Oc4ccc(-c5cnc6ccccc6n5)cc4)ccnc3NC2=O)cc1
Reaction #292859
DOI: 10.1039/C8SC04228D
Brc1ccc(-c2cnc3ccccc3n2)cc1
Reaction #338940
2-(4-bromo-phenyl)-quinoxaline
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
Brc1c2ccccc2c(-c2ccc(-c3cnc4ccccc4n3)cc2)c2ccccc12
Reaction #338941
2-[4-(10-bromo-anthracen-9-yl)-phenyl]-quinoxaline
Ausbeute 520.9%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC(=O)Nc1cccc(-c2cnc3ccccc3n2)c1
Reaction #380360
DOI: 10.1039/C8SC04228D
O=C(Nc1cccc(-c2cnc3ccccc3n2)c1)C1CC1
Reaction #395046
DOI: 10.1039/C8SC04228D
c1ccc([C@@H]2CNc3ccccc3N2)cc1
Reaction #607967
(R)-1,2,3,4-tetrahydro-2-phenylquinoxaline
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCl)Nc1cccc(-c2cnc3ccccc3n2)c1
Reaction #765191
DOI: 10.1039/C8SC04228D
CC(Cl)C(=O)Nc1cccc(-c2cnc3ccccc3n2)c1
Reaction #785704
DOI: 10.1039/C8SC04228D
O=C(Nc1cccc(-c2cnc3ccccc3n2)c1)c1ccco1
Reaction #894179
DOI: 10.1039/C8SC04228D
CS(=O)(=O)Nc1cccc(-c2cnc3ccccc3n2)c1
Reaction #901648
DOI: 10.1039/C8SC04228D
NS(=O)(=O)CCC(=O)Nc1cccc(-c2cnc3ccccc3n2)c1
Reaction #909064
DOI: 10.1039/C8SC04228D
COc1ccc(CN2Cc3c(Oc4ccc(-c5cnc6ccccc6n5)cc4)ccnc3NC2=O)cc1
Reaction #1132690
280
Ausbeute 42.7%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2cnc3ccccc3n2)cc1
Reaction #1285094
phenylquinoxaline
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cccc(-c2cnc3ccccc3n2)c1
Reaction #1319923
DOI: 10.1039/C8SC04228D
CNC(=S)Nc1cccc(-c2cnc3ccccc3n2)c1
Reaction #1631390
DOI: 10.1039/C8SC04228D
CCC(=O)Nc1cccc(-c2cnc3ccccc3n2)c1
Reaction #1637268
DOI: 10.1039/C8SC04228D
Nc1cccc(-c2cnc3ccccc3n2)c1
Reaction #2133092
(3-quinoxalin-2-ylphenyl)amine
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCl)Nc1cccc(-c2cnc3ccccc3n2)c1
Reaction #2133093
2-chloro-N-(3-quinoxalin-2-ylphenyl)acetamide
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
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