27개 반응에 참여

37503

N#CC(CCC(=O)N1CCC(Oc2ccccc2)CC1)(c1ccccc1)c1ccccc1
Reaction #183582
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(CN1CCC(Oc2ccccc2)CC1)Nc1ccc2c(c1)OCC(=O)N2
Reaction #236685
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(NCCN1CCC(Oc2ccccc2)CC1)Nc1ccnc2ccccc12
Reaction #263657
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
N#CCN1CCC(Oc2ccccc2)CC1
Reaction #271685
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Nc1ncc(Br)c(N2CCC(Oc3ccccc3)CC2)c1[N+](=O)[O-]
Reaction #504052
product
수율 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
O=C(O)C(=O)O.O[C@H](COc1cccc2[nH]ccc12)CN1CCC(Oc2ccccc2)CC1
Reaction #568784
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_08
N#CCN1CCC(Oc2ccccc2)CC1
Reaction #642944
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
NCCc1ccccc1
Reaction #696852
benzylmethylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_12
NCCc1ccccc1
Reaction #930169
benzylmethylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_04
c1ccc(OC2CCNCC2)cc1
Reaction #951435
4-phenoxypiperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_10
O=C1COc2cc(NC(=O)C(=O)N3CCC(Oc4ccccc4)CC3)ccc2N1
Reaction #1037774
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
O=C(O)C(=O)O.O[C@H](COc1cccc2[nH]ccc12)CN1CCC(Oc2ccccc2)CC1
Reaction #1064508
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_03
CS(=O)(=O)Nc1ccc(NCC(=O)N2CCC(Oc3ccccc3)CC2)cc1
Reaction #1207737
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
O=C1CCC(N2Cc3c(OCc4ccc(CN5CCC(Oc6ccccc6)CC5)cc4)cccc3C2=O)C(=O)N1
Reaction #1226502
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
c1ccc(OC2CCNCC2)cc1
Reaction #1653699
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
O=C(O)C(=O)O.O[C@H](COc1cccc2[nH]ccc12)CN1CCC(Oc2ccccc2)CC1
Reaction #1686739
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_04
O=C(O)C(=O)O.O[C@H](COc1cccc2[nH]ccc12)CN1CCC(Oc2ccccc2)CC1
Reaction #1866769
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_05
NCCc1ccccc1
Reaction #1944041
benzylmethylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_11
O=C(O)C(=O)O.O[C@H](COc1cccc2[nH]ccc12)CN1CCC(Oc2ccccc2)CC1
Reaction #1988124
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_11
c1ccc(OC2CCNCC2)cc1
Reaction #2042358
4-phenoxypiperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_09
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