2-acetylfuran

Cc1ncsc1C(C)(O)c1ccco1
Reaction #2913
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1nn(C)c(C)c1C(C)(O)c1ccco1
Reaction #2925
1-(2-Furyl)-1-(1,3,5-trimethyl-4-pyrazolyl)ethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc(C(CC(=O)c2ccco2)CC(=O)c2ccco2)c(OC)c1
Reaction #5645
1,5-Di(2-furyl)-3-(2,4-dimethoxyphenyl)-1,5-pentanedione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O[C@H](CCl)c1ccco1
Reaction #51984
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOC(=O)C(=O)CC(=O)c1ccco1
Reaction #61525
4-Furan-2-yl-2,4-dioxo-butyric acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC1(c2ccco2)OCCO1
Reaction #71023
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(O)C=CC(=O)c1ccco1
Reaction #214169
title compound
収率 21.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
O=C(CC(=O)C(F)(F)C(F)(F)C(F)(F)F)c1ccco1
Reaction #217478
4,4,5,5,6,6,6-Heptafluoro-1-(2-furyl)-1,3-hexanedione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCOC(=O)CC(=O)c1ccco1
Reaction #238791
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)C=Cc1ccc(C(C)=O)o1
Reaction #241033
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(C=Cc1ccncc1)c1ccco1
Reaction #253237
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(c1ccco1)N1CCOCC1
Reaction #265127
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(=O)c1ccc(Cc2ccc(F)cc2)o1
Reaction #283288
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(=O)c1ccc(Cc2ccc(F)cc2)o1
Reaction #286623
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=CC(=O)c1ccco1
Reaction #335661
α-oxo-2-furanacetaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CN(C)CCC(=O)c1ccco1.Cl
Reaction #360843
crystals
収率 13.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
CCOC(=O)C(=O)CC(=O)c1ccco1
Reaction #377220
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1nn(C)c(C)c1C(C)(O)c1ccco1
Reaction #392461
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(=O)c1ccc(Cc2ccc(F)cc2)o1
Reaction #394048
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(C)OC(=S)CC(=O)c1ccco1
Reaction #394397
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
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