(3RS)-3-(N-tert-butyloxycarbonylaminoethyl) pyrrolidine

N=C(NC(=O)OCc1ccccc1)N1CCC(CCN)C1
Reaction #965
title compound
Ausbeute 67.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N=C(NC(=O)OCc1ccccc1)N1CCC(CCN)C1
Reaction #428990
title compound
Ausbeute 67529.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
N=C(NC(=O)OCc1ccccc1)N1CCC(CCN)C1
Reaction #1537895
title compound
Ausbeute 67529.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_02
CCOC(=O)c1cc(CC)c2c(OC)c(N3CCC(CCNC(=O)OC(C)(C)C)C3)ccn2c1=O
Reaction #1659646
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
N=C(NC(=O)OCc1ccccc1)N1CCC(CCN)C1
Reaction #1672676
title compound
Ausbeute 67529.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_08
N=C(NC(=O)OCc1ccccc1)N1CCC(CCN)C1
Reaction #1697993
title compound
Ausbeute 67529.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_01
CCOC(=O)c1cc(CC)c2c(OC)c(N3CCC(CCNC(=O)OC(C)(C)C)C3)ccn2c1=O
Reaction #1722276
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_01
COc1c(N2CCC(CCN)C2)ccn2c(=O)c(C(=O)O)cc(C3CC3)c12
Reaction #1722279
8-[3-aminoethyl-pyrrolidinyl]-1-cyclopropyl-9-methoxy-4-oxo-4H-quinolizine-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_01
N=C(NC(=O)OCc1ccccc1)N1CCC(CCN)C1
Reaction #2043980
title compound
Ausbeute 67529.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_07
N=C(NC(=O)OCc1ccccc1)N1CCC(CCN)C1
Reaction #2044332
title compound
Ausbeute 67529.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_07