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873751

COc1cc2c(cc1OC)CN(c1c(C)c(C)c3c(c1C)[C@@H](c1ccc(C)cc1)C(C)(C)O3)C2
Reaction #57401
title compound
Ausbeute 75.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(OC)c(OC)cc1C1=NCCc2ccccc21
Reaction #93967
1-(4,5-Dimethoxy-2-methoxycarbonylphenyl)-3,4-dihydroisoquinoline
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1OC)C1(O)c3ccccc3CCN1C2=O
Reaction #93968
12b-Hydroxy-10,11-dimethoxy-5,6,8,12b-tetrahydro-isoindolo[1,2-a]isoquinol-8-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1OC)C(O)N(CCc1ccccc1)C2=O
Reaction #93969
3-Hydroxy-2-phenethyl-5,6-dimethoxy-2,3-dihydro-1H-isoindol-1-one
Ausbeute 96.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1OC)CNC2
Reaction #174003
DOI: 10.1039/C8SC04228D
COc1cc2c(cc1OC)CN(CCc1ccc(N)cc1)C2
Reaction #213085
DOI: 10.1039/C8SC04228D
Br.CCOc1cc2c(c(F)c1OCC)C(=N)N(CC(=O)c1cc(N3CCOCC3)c(OC)c(C(C)(C)C)c1)C2
Reaction #331519
captioned compound
Ausbeute 91.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1OC)CN(c1c(C)c(C)c3c(c1C)C(c1ccccc1)C(C)(C)O3)C2
Reaction #359508
title compound
Ausbeute 26.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1OC)CN(c1c(C)c(C)c3c(c1C)C(c1ccc(C)cc1)C(C)(C)O3)C2
Reaction #359510
title compound
Ausbeute 16.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1OC)C(=O)N(c1c(C)c(C)c3c(c1C)C(c1ccc(C)cc1)C(C)(C)O3)C2=O
Reaction #359520
(+)-5,6-dimethoxy-2-[2,2,4,6,7-pentamethyl-3-(4-methylphenyl)-2,3-dihydro-1-benzofuran-5-yl]-1H-isoindole-1,3(2H)-dione
Ausbeute 85.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1OC)CN(c1c(C)c(C)c3c(c1C)C(c1ccc(C)cc1)C(C)(C)O3)C2.Cl
Reaction #359521
titled compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(C2c3c(C)c(N4Cc5cc(OC)c(OC)cc5C4)c(C)c(C)c3OC2(C)C)cc1.Cl
Reaction #359522
title compound
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
Br.COc1cc2c(cc1OC)CN(c1c(C)c(C)c3c(c1C)C(c1ccc(C)cc1)C(C)(C)O3)C2
Reaction #359523
title compound
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(CCCCCCN2Cc3cc(OC)c(OC)cc3C2)Sc2ccc(C)cc2)cc1OC
Reaction #361183
desired product
Ausbeute 61.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(CCCCCCN2CCc3cc(OC)c(OC)c(OC)c3C2)Sc2ccc(C)cc2)cc1OC
Reaction #361189
desired product
Ausbeute 65.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1OCc1ccccc1)CN(Cc1ccccc1)C2
Reaction #361198
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1O)CNC2
Reaction #361199
desired product
Ausbeute 87.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1OC)CN(c1c(C)c(C)c3c(c1C)C(c1ccc(C)cc1)C(C)(C)O3)C2
Reaction #380087
DOI: 10.1039/C8SC04228D
COc1cc2c(cc1OC)C(=O)N(c1ccc(Cl)cc1)C2
Reaction #392676
DOI: 10.1039/C8SC04228D
COc1cc2c(cc1OC)CN(CCCCCCN(Cc1ccccn1)Cc1ccccc1OC(C)(C)C)C2
Reaction #490301
oil
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
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