Impliqué dans 407 réactions

C1CNCCC12OCCO2

c1ccc(N2CCC3(CC2)OCCO3)nc1
Reaction #332
Rendement 66.6%750 AstraZeneca ELN dataset
COc1cncc(N2CCC3(CC2)OCCO3)c1
Reaction #550
Rendement 75.1%750 AstraZeneca ELN dataset
COc1cccc(N2CCC3(CC2)OCCO3)n1
Reaction #576
Rendement 69.1%750 AstraZeneca ELN dataset
Cc1ccc(C(=O)Nc2c(NC(=O)CN3CCC4(CC3)OCCO4)ccc3c2C(=O)c2ccccc2C3=O)cc1
Reaction #69054
1-(4-methylbenzamido)-2-[2-(1,4-dioxa-8-azaspiro[4.5]dec-8-yl)acetylamino]-anthraquinone
Rendement 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Brc1ccc(N2CCC3(CC2)OCCO3)cc1
Reaction #69978
8-(4-bromophenyl)-1,4-dioxa-8-azaspiro[4.5]decane
Rendement 58.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C1CC2(CCN1)OCCO2
Reaction #81439
8-aza-1,4-dioxaspiro-[4,5]decane
Rendement 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C(C(Cl)Cl)N1CCC2(CC1)OCCO2
Reaction #93665
N-dichloroacetylpiperid-4-one ethylene ketal
Rendement 49.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
Clc1cnc(N2CCC3(CC2)OCCO3)nc1
Reaction #155972
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Fc1cc(C(F)(F)F)cnc1N1CCC2(CC1)OCCO2
Reaction #155973
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCc1cnc(N2CCC3(CC2)OCCO3)nc1
Reaction #155974
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCc1nc(CC)n(-c2ccc(N3CCC4(CC3)OCCO4)cc2)c(=O)c1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #173934
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(N2CCC3(CC2)OCCO3)ccc1Cl
Reaction #174818
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Brc1ccc(N2CCC3(CC2)OCCO3)cc1
Reaction #183976
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(F)cc1S(=O)(=O)N1CCC2(CC1)OCCO2
Reaction #184842
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1ccc2nc(N3CCC4(CC3)OCCO4)ccc2c1
Reaction #193185
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)c1ccc(N2CCC3(CC2)OCCO3)cc1
Reaction #193931
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCN1CC(C)N(C(c2cccc(O)c2)c2cccc(C(=O)N3CCC4(CC3)OCCO4)c2)CC1C
Reaction #194055
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(N2CCC3(CC2)OCCO3)ccc1[N+](=O)[O-]
Reaction #194867
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1noc(N2CCC3(CC2)OCCO3)n1
Reaction #196779
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(C(Cl)Cl)N1CCC2(CC1)OCCO2
Reaction #198568
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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