4-oxo-cyclohexane carboxylic acid ethyl ester

CCOC(=O)C1CCNC(=O)CC1
Reaction #7496
ester
Rendement 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)C1CCC(=O)C(Br)C1
Reaction #40322
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C1CCC2(CC1)OCCO2
Reaction #40917
1,4-dioxa-spiro[4.5]decane-8-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Br.CCOC(=O)C1CCc2nc(N)sc2C1
Reaction #46957
title product
Rendement 47.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
OCC1CCC2(CC1)OCCO2
Reaction #59985
title compound
Rendement 85.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
OCC1CCC(O)CC1
Reaction #69248
4-(Hydroxymethyl)cyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
OCC1CCC(O)CC1
Reaction #73279
4-(Hydroxymethyl)cyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)C1CCc2[nH]ncc2C1
Reaction #87162
ethyl 4,5,6,7-tetrahydro-1H-indazole-5-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)C1CCC(C)(O)CC1
Reaction #87169
ethyl 4-hydroxy-4-methylcyclohexanecarboxylate
Rendement 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
N[C@@]1(C(=O)O)CN(C2CCC(C(=O)O)CC2)C[C@@H]1CCCB(O)O
Reaction #89654
(3R,4S)-3-amino-4-(3-boronopropyl)-1-(4-carboxycyclohexyl)pyrrolidine-3-carboxylic acid
Rendement 78.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)C1CCC2(CC1)OCCO2
Reaction #164104
raw product
Rendement 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)C1CCC(N2CC(NC(=O)CNc3nn(C)c4ccc(C(O)C(F)(F)F)cc34)C2)CC1
Reaction #174933
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C1CCC(O)(c2ccc(Cl)cn2)CC1
Reaction #177601
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C1CCC(N2CC(NC(=O)CNc3nn(C)c4ccc(C(F)(F)F)cc34)C2)CC1
Reaction #179291
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C1CCC(Nc2nnc[nH]2)CC1
Reaction #190868
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C1CCC(=O)C(Br)C1
Reaction #204551
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C1CCC2(CC1)OCCO2
Reaction #229188
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)C1CCC2(CC1)OCCO2
Reaction #231571
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)C1CCC2(CC1)OCCO2
Reaction #236085
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)C1CCC2(CC1)OCCO2
Reaction #243345
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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