Teilstruktursuche

1162857

CC(C)CS(=O)(=O)c1ccc2cc(N)c(N)cc2c1
Reaction #236349
DOI: 10.1039/C8SC04228D
O=c1[nH]c2cc3ccccc3cc2nc1-c1cc(O)c(O)c([N+](=O)[O-])c1
Reaction #361643
3-(3,4-dihydroxy-5-nitrophenyl)-benzo[g]quinoxalin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N(c2ccc(C)cc2)c2cc3c4cccc5cc6ccccc6c(c6cccc(c2N(c2ccc(C)cc2)c2ccc(C)cc2)c36)c54)cc1
Reaction #440595
bis(di-p-tolylamino)benzo[a]perylene
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2nc3cc4ccccc4cc3nc2cc1C
Reaction #463735
2,3-dimethylbenzo(B)phenazine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2nc3cc4ccccc4cc3nc2cc1C
Reaction #697960
2,3-dimethylbenzo(B)phenazine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CSc1ccc2cc([N+](=O)[O-])c(N)cc2c1
Reaction #772940
DOI: 10.1039/C8SC04228D
O=c1[nH]c2cc3ccccc3cc2nc1-c1cc(O)c(O)c([N+](=O)[O-])c1
Reaction #812508
3-(3,4-dihydroxy-5-nitrophenyl)benzo[g]quinoxalin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
BrCc1nc2cc3ccccc3cc2nc1CBr
Reaction #979594
2,3-bis(bromomethyl)benzo[g]quinoxaline
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2c(c1)Nc1cc3ccccc3cc1N2
Reaction #983146
5,12-dihydro-benzo[b]phenazine
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(cc1C)Nc1cc3ccccc3cc1N2
Reaction #983147
5,12-dihydro-2,3-dimethyl-benzo[b]phenazine
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCNc1cc2ccccc2cc1N
Reaction #1034896
DOI: 10.1039/C8SC04228D
c1ccc2c(c1)Nc1cc3ccccc3cc1N2
Reaction #1071940
5,12-dihydro-benzo[b]phenazine
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(cc1C)Nc1cc3ccccc3cc1N2
Reaction #1071941
5,12-dihydro-2,3-dimethyl-benzo[b]phenazine
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc3ccccc3cc2[nH]c1=O
Reaction #1072026
title compound
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc2ccc(Cl)cc2cc1N
Reaction #1223769
DOI: 10.1039/C8SC04228D
O=c1[nH]c2cc3ccccc3cc2[nH]c1=O
Reaction #1273634
benzo[g]quinoxaline-2,3(1H,4H)-dione
Ausbeute 104.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N(c2ccc(C)cc2)c2cc3c4cccc5cc6ccccc6c(c6cccc(c2N(c2ccc(C)cc2)c2ccc(C)cc2)c36)c54)cc1
Reaction #1332434
bis(di-p-tolylamino)benzo[a]perylene
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc2ccccc2cc1NC(=O)c1cc2cc(Cl)ccc2[nH]1
Reaction #1441455
title compound
Ausbeute 24.1%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@H]1/C=C/O[C@@]2(C)Oc3c(C)c(O)c4c(O)c(c(N5CCC(C)CC5)c(O)c4c3C2=O)NC(=O)/C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C
Reaction #1502591
3-(4-methylpiperidino)-rifamycin
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCNc1cc2ccccc2cc1N
Reaction #1618944
product
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter