furfural

CCC(C)C(NCc1ccco1)C(=O)OC
Reaction #280936
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
NC(C(=O)O)C(O)c1ccco1
Reaction #285966
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
N#CC(N)c1ccco1
Reaction #290849
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C(=Cc1ccco1)c1cccnc1
Reaction #294316
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Nc1cc(NCc2ccco2)cc(C(=O)O)c1
Reaction #322972
3-amino-5-(N-furfurylamino)benzoic Acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
CC(C)(C)[S@](=O)/N=C/c1ccco1
Reaction #333127
(S)-2-methyl-propane-2-sulfinic acid 1-furan-2-yl-meth-(E)-ylideneamide
Ausbeute 89.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
NC(C(=O)O)C(O)c1ccco1
Reaction #345406
α-Amino-β-hydroxy-β-(2-furyl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
CC(C#N)C(=O)c1ccco1
Reaction #346125
α-furoylpropionitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
O=C(c1ccccc1)C1(c2ccccc2)COC(c2ccco2)O1
Reaction #346532
2-furyl-4-benzoyl-4-phenyl-1, 3-dioxolane
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
O=C(c1ccccc1)C1(c2ccccc2)COC(c2ccco2)O1
Reaction #354885
2-furyl-4-benzoyl-4-phenyl-1,3-dioxolane
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1976_03
O=Cc1ccc(-c2ccc(OCc3ccccc3)cc2)o1
Reaction #355269
5-(p-Benzyloxyphenyl)-2-furaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1976_03
COc1ccc(-c2ccc(C=O)o2)cc1
Reaction #355278
black semi-solid
Ausbeute 23.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1976_03
O=C(O)C=Cc1ccco1
Reaction #360849
2-furanacrylic acid
Ausbeute 18.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
CCCCC(O)c1ccco1
Reaction #361607
Racemic 1-(2-furyl)-1-pentanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
CC(C)(C)OC(=O)NCc1cccc(C(O)c2cc(Cl)ccc2NCc2ccco2)c1
Reaction #363056
5-chloro-2-(furan-2-ylmethyl)amino-α-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol
Ausbeute 98.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Nc1cc(Br)cc2nc(-c3ccco3)nn12
Reaction #364240
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CC(C)C(=O)C=Cc1ccco1
Reaction #392402
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C1NC(=O)C(N2Cc3c(NCc4ccco4)cccc3C2=O)CC1O
Reaction #393786
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C1NC(=O)c2ccc(I)cc2C1=CNc1ccc(N2CCN(Cc3ccco3)CC2)cc1
Reaction #398481
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1cc(N=Cc2ccco2)c(C(=O)O)cc1S(C)(=O)=O
Reaction #405818
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
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