1-benzhydrylazetidin-3-ol

O=C1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #56751
title compound
Ausbeute 170.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cl.OC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #70357
1-(diphenylmethyl)-3-hydroxyazetidine hydrochloride
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CS(=O)(=O)OC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #170096
title compound
Ausbeute 96.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
c1ccc(C(c2ccccc2)N2CC(OCc3cccs3)C2)cc1
Reaction #170111
1-(Diphenylmethyl)-3-(2-thienylmethoxy)azetidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCCCOC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #170119
title compound
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
c1ccc(COC2CN(C(c3ccccc3)c3ccccc3)C2)cc1
Reaction #170124
product
Ausbeute 24.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=C(C)COC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #170131
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1c2ccccc2C(=O)N1OC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #170138
title compound
Ausbeute 37.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
—
Reaction #170162
solid
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
—
Reaction #170240
solid
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #170262
1-benzhydrylazetidin-3-one
Ausbeute 105.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Clc1ccc(COC2CN(C(c3ccccc3)c3ccccc3)C2)cc1Cl
Reaction #173600
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #188021
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CS(=O)(=O)OC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #188153
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CS(=O)(=O)OC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #192639
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cccc(Cl)c1OC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #197968
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(OCc1ccccc1)N1CC(O)C1
Reaction #203756
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Clc1ccc(OC2CN(C(c3ccccc3)c3ccccc3)C2)cc1Cl
Reaction #208457
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(C(=O)N2CC(O)C2)ncc1C(c1cc(F)ccc1F)S(=O)(=O)c1ccc(F)cc1
Reaction #222483
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Brc1ccc(OC2CN(C(c3ccccc3)c3ccccc3)C2)nc1
Reaction #222815
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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