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10851

c1ccc2c(c1)OC(c1ccc(OCCN3CCCCC3)cc1)c1c-2sc2ccccc12
Reaction #1804
title compound
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC1CCN(c2cnc(C(=O)Nc3cc(CCc4cc(OC)cc(OC)c4)n[nH]3)cn2)C1
Reaction #45153
title compound
Ausbeute 39.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cc2cnc(N)nc2N)c2c(c1OC)OC(C)CC2=O
Reaction #62723
title compound
Ausbeute 29.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCc2ccccc2)cc(C2=Nc3cc4c(cc3C(=O)C2)OCO4)c1
Reaction #66937
2-(3-Benzyloxy-5-methoxyphenyl)-6,7-methylenedioxyquinolin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(O)cc(C2=Nc3cc4c(cc3C(=O)C2)OCO4)c1
Reaction #66938
166
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN(c2ncns2)S(=O)(=O)c2cc(F)c(Oc3ccc(Cl)cc3-c3ccnn3C3CN(C(=O)OC(C)(C)C)C3)cc2F)c(OC)c1
Reaction #74649
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN(c2ncns2)S(=O)(=O)c2ccc(Oc3ccc(C(F)(F)F)cc3-c3ccnn3C3CN(C(=O)OC(C)(C)C)C3)c(C#N)c2)c(OC)c1
Reaction #74674
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(N(COCC[Si](C)(C)C)C(=O)N(C)c2cc(Cl)ncn2)c1Cl
Reaction #86419
title compound
Ausbeute 28.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(N(COCC[Si](C)(C)C)C(=O)N(C)c2cc(Nc3ccc(C4CCN(C(=O)OC(C)(C)C)CC4)cc3N)ncn2)c1Cl
Reaction #86420
title compound
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(N(COCC[Si](C)(C)C)C(=O)N(C)c2cc(Nc3ccc(CN(C)C)cc3[N+](=O)[O-])ncn2)c1Cl
Reaction #86425
desired product
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(N(COCC[Si](C)(C)C)C(=O)N(C)c2cc(Nc3ccc(N4CCOCC4)cc3[N+](=O)[O-])ncn2)c1Cl
Reaction #86433
title compound
Ausbeute 51.7%DOI: 10.6084/m9.figshare.5104873.v1
CC#CC(=O)Nc1ccccc1Nc1cc(N(C)C(=O)Nc2c(Cl)c(OC)cc(OC)c2Cl)ncn1
Reaction #86438
title compound
Ausbeute 50.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(N(C(=O)OC(C)(C)C)C(=O)N(C)c2cc(N(C(=O)OC(C)(C)C)c3ccc(C(=O)O)cc3[N+](=O)[O-])ncn2)c1Cl
Reaction #86465
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(N(C(=O)OC(C)(C)C)C(=O)N(C)c2cc(N(C(=O)OC(C)(C)C)c3ccc(C(=O)N4CCN(C)CC4)cc3[N+](=O)[O-])ncn2)c1Cl
Reaction #86466
title compound
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(N(COCC[Si](C)(C)C)C(=O)N(C)c2cc(Nc3ccc(N4CCN(C(=O)OC(C)(C)C)CC4)cc3[N+](=O)[O-])ncn2)c1Cl
Reaction #86480
title compound
Ausbeute 45.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(N(COCC[Si](C)(C)C)C(=O)N(C)c2cc(N(C(=O)OC(C)(C)C)c3ccc(N4CCN(C(=O)OC(C)(C)C)CC4)cc3N)ncn2)c1Cl
Reaction #86481
crude title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)Nc1cc(N2CCN(CCN)CC2)ccc1Nc1cc(N(C)C(=O)Nc2c(Cl)c(OC)cc(OC)c2Cl)ncn1
Reaction #86488
title compound
Ausbeute 136.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(OC)c1-c1cncc(N2CC3CC4CC2CN(C4)C3)c1
Reaction #167607
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cncc(N3CC4CC5CC3CN(C5)C4)c2)c(OC)c1
Reaction #167623
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(Nc2ccc(C(=N)N)cc2)c2nn(-c3ccsc3C(=O)O)c(=O)[nH]2)c(F)c2c1OCC2
Reaction #174724
DOI: 10.1039/C8SC04228D
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