4-aminocyclohexan-1-ol

CC1=C(C)C(=O)N(C2CCC(O)CC2)C1=O
Reaction #74881
N-(4-hydroxycyclohexyl)-dimethyl-maleimide
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
CC(C)C(=O)NC1CCC(O)CC1
Reaction #172991
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(c1ccccc1)c1nc2cc(F)ccc2n1C(C(=O)NC1CCC(O)CC1)C1CCCCC1
Reaction #181622
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1CCCN1C1CCC(O)CC1
Reaction #181831
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OC1CCC(Nc2ncc3cccc(Br)c3n2)CC1
Reaction #186078
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1c2ccccc2C(=O)N1C1CCC(O)CC1
Reaction #197163
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OC1CCC(NCc2ccc(Cl)cc2)CC1
Reaction #198847
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1nn(-c2ccnc(NC3CCC(O)CC3)n2)c2ccccc12
Reaction #199299
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)[Si](C)(C)OC1CCC(N)CC1
Reaction #204109
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OC1CCC(NC2CCCCC2)CC1
Reaction #204161
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCN1C(=O)N(c2cc(OC)cc(OC)c2F)Cc2cnc(NC3CCC(O)CC3)nc21
Reaction #204374
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccc(CNC2CCC(O)CC2)cc1
Reaction #206705
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OC1CCC(NC(c2ccccc2)(c2ccccc2)c2ccccc2)CC1
Reaction #227503
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(NC1CCC(O)CC1)OCc1ccccc1
Reaction #228249
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
NC1CCC(OC(=O)c2ccccc2)CC1
Reaction #235432
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C[Si](C)(C)OC1CCC(N)CC1
Reaction #235528
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(NCc1ccc2c(c1)OCO2)c1cc([N+](=O)[O-])ccc1NC1CCC(O)CC1
Reaction #237497
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#Cc1cnc(NC2CCC(O)CC2)c([N+](=O)[O-])c1
Reaction #244390
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
OC1CCC(Nc2ncc3cccc(OC4CCOCC4)c3n2)CC1
Reaction #245546
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=S(=O)(NC1CCC(O)CC1)c1ccc(C(F)(F)F)cc1
Reaction #245648
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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