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39974

Nc1n[nH]c(-c2cccnc2)c1-c1nc2ccccc2s1
Reaction #85548
desired product
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
Brc1cc(-c2cccnc2)cc(-c2nc3ccccc3s2)c1
Reaction #478682
2-(3-bromo-5-(pyridin-3-yl)phenyl)benzo[d]thiazole
DOI: 10.6084/m9.figshare.5104873.v1
Nc1n[nH]c(-c2cccnc2)c1-c1nc2ccccc2s1
Reaction #494511
desired product
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])c1ccc2cccc(O)c2n1.O=C([O-])c1ccc2cccc(O)c2n1.O=C([O-])c1ccc2cccc(O)c2n1.[Ir+3].c1ccc(-c2nc3ccccc3s2)cc1.c1ccc(-c2nc3ccccc3s2)cc1
Reaction #581072
Bis(2-phenylbenzothiazole) Iridium (8-hydroxyquinolate)
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])c1ccccn1.O=C([O-])c1ccccn1.O=C([O-])c1ccccn1.[Ir+3].c1ccc(-c2nc3ccccc3s2)cc1.c1ccc(-c2nc3ccccc3s2)cc1
Reaction #581073
impure product
Ausbeute 229.3%DOI: 10.6084/m9.figshare.5104873.v1
O=c1nc(-c2cccnc2)sc2ccccc12
Reaction #1094309
title compound
Ausbeute 43.4%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc2nc(-c3ccccc3)sc2c1
Reaction #1291826
DOI: 10.1039/C8SC04228D
S=C=Nc1ccc2sc(-c3cccnc3)nc2c1
Reaction #1301554
DOI: 10.1039/C8SC04228D
c1cncc(-c2nc3ccccc3s2)c1
Reaction #1375011
2-(3-Pyridinyl)benzothiazole
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2sc(-c3cccnc3)nc2c1
Reaction #1375013
product
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
S=C=Nc1ccc2sc(-c3cccnc3)nc2c1
Reaction #1375014
white solid
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])c1ccc2cccc(O)c2n1.O=C([O-])c1ccc2cccc(O)c2n1.O=C([O-])c1ccc2cccc(O)c2n1.[Ir+3].c1ccc(-c2nc3ccccc3s2)cc1.c1ccc(-c2nc3ccccc3s2)cc1
Reaction #1449970
Bis(2-phenylbenzothiazole) Iridium (8-hydroxyquinolate)
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])c1ccccn1.O=C([O-])c1ccccn1.O=C([O-])c1ccccn1.[Ir+3].c1ccc(-c2nc3ccccc3s2)cc1.c1ccc(-c2nc3ccccc3s2)cc1
Reaction #1449971
impure product
Ausbeute 229.3%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2nc3ccccc3s2)cc1
Reaction #1452774
2-phenylbenzothiazole
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2sc(-c3ccncc3)nc2c1
Reaction #1544995
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
C1=C(c2nc3ccccc3s2)CCN(Cc2ccccc2)C1
Reaction #1544996
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
Brc1cc(-c2cccnc2)cc(-c2nc3ccccc3s2)c1
Reaction #1708488
2-(3-bromo-5-(pyridin-3-yl)phenyl)benzo[d]thiazole
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(F)cc1
Reaction #1792034
DOI: 10.1021/acscatal.0c02247
CC(=O)c1ccc(F)cc1
Reaction #1792082
DOI: 10.1021/acscatal.0c02247
CCN(CC)c1ccc2oc(=O)c(-c3[nH+]c4ccccc4s3)cc2c1.[Br-]
Reaction #1792130
DOI: 10.1021/acscatal.0c02247
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