Ähnlichkeitssuche

25449

Fc1ccc(CC[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1.[Br-]
Reaction #40647
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(Nc3c(Cl)cncc3Cl)cc(=O)oc2c1OCCc1ccccc1
Reaction #48943
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#CC(c1ccccc1)(c1ccccc1)[C@H]1CCCN(CCc2ccc(Cl)cc2)C1
Reaction #49663
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#CC(c1ccccc1)(c1ccccc1)[C@H]1CCCN(CCc2ccccc2)C1
Reaction #49664
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#CC(c1ccccc1)(c1ccccc1)[C@H]1CCCN(CCc2ccc(CO)cc2)C1
Reaction #49665
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CCN2CCC[C@H](C(C#N)(c3ccccc3)c3ccccc3)C2)cc1
Reaction #49667
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#CC(c1ccccc1)(c1ccccc1)C1CCCN(CCc2ccc(O)cc2)C1
Reaction #49670
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CCN2CCCC(C(C(N)=O)(c3ccccc3)c3ccccc3)C2)cc1
Reaction #49674
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C(c1ccccc1)(c1ccccc1)C1CCCN(CCc2ccccc2)C1
Reaction #49675
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C(c1ccccc1)(c1ccccc1)C1CCCN(CCc2ccc(Cl)cc2)C1
Reaction #49676
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C(c1ccccc1)(c1ccccc1)C1CCCN(CCc2ccc(O)cc2)C1
Reaction #49677
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C/C=C/COC(C)C1=CC(C)(C)Nc2ccc(-c3ccccc3OC)cc21
Reaction #54069
title compound
Ausbeute 140.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc([C@@]23CCCC[C@@H]2C(=O)N(CCc2ccccc2)C(=O)C3)c1
Reaction #54757
N-Phenethyl-4a-(m-methoxyphenyl)-1,3-diketo-cis-decahydroisoquinoline
DOI: 10.6084/m9.figshare.5104873.v1
N#CC(CCc1ccccc1)c1ccc(Cl)cc1Cl
Reaction #56543
α-phenethyl-2,4-dichlorobenzyl cyanide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CCN(C)CCC(=O)N2c3ccccc3NC(=O)c3ccccc32)cc1
Reaction #65132
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN(CCc2ccccc2)c2ccc3[nH]cnc3c2)cc1
Reaction #74249
N-(4-Methoxybenzyl)-N-phenethyl-1H-benzo[d]imidazol-5-amine
DOI: 10.6084/m9.figshare.5104873.v1
Br.COc1ccc(CCNCCc2ccccc2)cc1OC
Reaction #75051
N-phenethyl-3,4-dimethoxyphenethylamine hydrobromide
Ausbeute 44.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2CN(CCc3ccc(Br)cc3)CCN2C(=O)N1c1cc(Cl)cc(Cl)c1
Reaction #78262
7-[2-(4-bromophenyl)ethyl]-2-(3,5-dichlorophenyl)-tetrahydro-imidazo[1,5-a]pyrazine-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(CCBr)cc1
Reaction #79556
2-(4-fluorophenyl)ethyl bromide
Ausbeute 64.8%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cn(CCc2ccccc2)cn1
Reaction #79576
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter