cyclobutane carboxylic acid

Clc1cc(C2CCC2)c(Cl)nn1
Reaction #11321
title compound
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCCC1(C(=O)O)CCC1
Reaction #55575
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCCCC1(C(=O)O)CCC1
Reaction #57060
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(=O)C1CCC1
Reaction #70753
ethyl cyclobutanecarboxylate
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)C1CCC1
Reaction #90652
ethyl cyclobutanecarboxylate
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
C=C(C)[C@@H]1CC[C@]2(NCCN3CCN(C(=O)C4CCC4)CC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172935
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)c1cc(NC(=O)C2CCC2)n[nH]1
Reaction #186992
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC1(C(=O)O)CCC1
Reaction #188592
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Nc1c[nH]c2ncc(Br)c(F)c12)C1CCC1
Reaction #206729
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)Cc1ccc(NC(=O)C2CCC2)cc1
Reaction #209957
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cccc(C)c1-c1cc(C2CCC2)c(Cl)nn1
Reaction #229760
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=O)C=CC1CCC1
Reaction #234712
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1nnc2ccc(-c3cccc(NC(=O)C4CCC4)c3)nn12
Reaction #237950
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
NC(N)=Nc1nc(-c2cccc(CNC(=O)C3CCC3)n2)cs1
Reaction #239797
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(NC1CCC(CCN2CCC(Oc3c(Cl)cc(F)cc3Cl)CC2)CC1)C1CCC1
Reaction #241727
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Clc1cc(C2CCC2)c(Cl)nn1
Reaction #242003
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)C(CS)NC(=O)C1CCC1
Reaction #267949
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(Nc1nc2ccc(OS(=O)(=O)c3ccc(F)cc3)cc2s1)C1CCC1
Reaction #275030
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCC1(C(=O)O)CCC1
Reaction #285926
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cn1c(S)nnc1C1CCC1
Reaction #306898
crude title product
Ausbeute 61.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
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