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474442

O=C([O-])c1cccnc1OC1CN(C2CCCCC2)C1.[Na+]
Reaction #4880
crude title compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
OC1(CSc2ccc(F)cc2)CN(C(c2ccccc2)c2ccccc2)C1
Reaction #10303
title product
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc([C@H](c2ccc(Cl)cc2)N2CC(=O)C2)cc1
Reaction #46334
1-{(R*)-(4-chlorophenyl)[4-(methoxycarbonyl)phenyl]methyl}azetidin-3-one
Ausbeute 83.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc([C@H](c2ccc(Cl)cc2)N2CC(O)C2)cc1
Reaction #46335
1-{(R*)-(4-chlorophenyl)[4-(methoxycarbonyl)-phenyl]methyl}azetidin-3-ol
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CN(C(c2cccs2)c2cccs2)C1
Reaction #53469
1-[bis(thien-2-yl)methyl]azetidin-3-one
Ausbeute 80.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #56751
title compound
Ausbeute 170.6%DOI: 10.6084/m9.figshare.5104873.v1
Cl.OC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #70357
1-(diphenylmethyl)-3-hydroxyazetidine hydrochloride
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1[C@H](OS(C)(=O)=O)CN1C(c1ccccc1)c1ccccc1
Reaction #72192
title compound
Ausbeute 90.9%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1[C@@H](O)CN1C(c1ccccc1)c1ccccc1
Reaction #72195
title compound
Ausbeute 29.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1[C@@H](OS(C)(=O)=O)CN1C(c1ccccc1)c1ccccc1
Reaction #72196
title compound
Ausbeute 32.3%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1[C@@H](N)CN1C(c1ccccc1)c1ccccc1
Reaction #72197
title compound
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(OC2CN(C(c3ccccc3)c3ccccc3)C2)cc1
Reaction #159581
title compound ( D20 )
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(OC2CN(C(c3ccccc3)c3ccccc3)C2)cc1
Reaction #159582
1-benzhydryl-3-(4-fluorophenoxy)azetidine
DOI: 10.6084/m9.figshare.5104873.v1
Fc1cccc(OC2CN(C(c3ccccc3)c3ccccc3)C2)c1
Reaction #159583
title compound
Ausbeute 80.9%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(NC2CN(C(c3ccccc3)c3ccccc3)C2)cc1
Reaction #159584
1-benzhydryl-N-(4-fluorophenyl)azetidin-3-amine
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(OC2CNC2)cc1
Reaction #159604
title compound ( D48 )
Ausbeute 37.1%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(OC2CNC2)cc1
Reaction #159605
title compound ( D49 )
Ausbeute 99.9%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CN(C(c2ccccc2)c2ccccc2)[C@H]1C
Reaction #168028
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(CCOc1cc2c(cc1F)CC(N1CC(C)(O)C1)C2Cc1ccccc1)S(=O)(=O)c1cn(C)cn1
Reaction #170078
N-(2-(3-benzyl-6-fluoro-2-(3-hydroxy-3-methylazetidin-1-yl)-2,3-dihydro-1H-inden-5-yloxy)ethyl)-N,1-dimethyl-1H-imidazole-4-sulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #170096
title compound
Ausbeute 96.5%DOI: 10.6084/m9.figshare.5104873.v1
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