3-(N-tert-butyloxycarbonylaminomethyl)-1-benzhydryl azetidine

CC(C)(C)OC(=O)NCC1CNC1
Reaction #966
title compound
Rendimiento 67.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)NCCC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #969
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)NCC1CNC1
Reaction #386292
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(C)(C)OC(=O)NCC1CNC1
Reaction #428995
title compound
Rendimiento 67.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CC(C)(C)OC(=O)NCCC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #783788
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CC(C)(C)OC(=O)NCC1CNC1
Reaction #1537896
title compound
Rendimiento 67.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_02
CC(C)(C)OC(=O)NCCC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #1537899
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_02
CC(C)(C)OC(=O)NCC1CNC1
Reaction #1672682
title compound
Rendimiento 67.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_08
CC(C)(C)OC(=O)NCCC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #1672685
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_08
CC(C)(C)OC(=O)NCC1CNC1
Reaction #1697999
title compound
Rendimiento 67.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_01
CC(C)(C)OC(=O)NCCC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #1698002
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_01
CC(C)(C)OC(=O)NCC1CNC1
Reaction #2043981
title compound
Rendimiento 67.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_07
CC(C)(C)OC(=O)NCCC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #2043983
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_07
CC(C)(C)OC(=O)NCC1CNC1
Reaction #2044333
title compound
Rendimiento 67.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_07
CC(C)(C)OC(=O)NCCC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #2044336
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_07