furfural

CCc1ccc(-c2ccc(Cl)cc2)cc1C(O)c1ccco1
Reaction #68748
(4′-chloro-4-ethylbiphen-3-yl)furan-2-ylmethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1ccnc(C(O)c2ccco2)c1C
Reaction #74947
2-furyl-(3,4-dimethyl-2-pyridyl)-carbinol
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
C(=Cc1ccco1)c1cccnc1
Reaction #80447
2-[2-{3-pyridyl}ethenyl]furan
Ausbeute 49.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
c1coc(-c2nc3cc(-c4nc5ccccc5o4)ccc3n2C2CCOCC2)c1
Reaction #161417
title compound
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)c1ccc(/C=C/c2ccco2)cc1
Reaction #165208
title compound
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=C(C)[C@@H]1CC[C@]2(NCc3ccco3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)OC)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172825
title compound
Ausbeute 90.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(=O)C(=Cc1ccco1)C(C)=O
Reaction #179765
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Fc1cccc(COc2cccc(CCNCc3ccco3)c2)c1
Reaction #180953
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Oc1cccc2ccc(C=Cc3ccco3)nc12
Reaction #186126
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCN(CC)C(=O)c1ccc(C(c2cccc(C#N)c2)N2CCN(Cc3ccco3)CC2)cc1
Reaction #193795
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])C=Cc1ccco1
Reaction #200718
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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Reaction #215840
product
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
COC(=O)c1cccc(NCc2ccco2)c1C(=O)OC
Reaction #226814
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(Cc1ccc(Cl)nc1)c1ccco1
Reaction #235303
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(N(C)c2ccco2)cc1O
Reaction #236538
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(O)CCCCCCCCCC=Cc1ccco1
Reaction #240189
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC1NC(=O)NN=C1c1ccc(N=Cc2ccco2)cc1
Reaction #245957
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)=CCCC(C)=CC=O
Reaction #257501
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)CCC(=O)c1ccco1
Reaction #263531
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
BrC(Br)=Cc1ccco1
Reaction #267440
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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