tetronic acid

O=C(CCCCCOc1ccc(Cl)cc1)C1=C(O)COC1=O
Reaction #5341
4-hydroxy-3-[6-(4-chlorophenoxy)-1-oxohexyl]-2(5H)-furanone
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCC/C=C\CCCCCCCC(=O)C1=C(O)COC1=O
Reaction #5342
4-hydroxy-3-((Z)-1-oxo-9-tetradecenyl)-2(5H)-furanone
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCCCC/C=C\CCCCCCCC(=O)C1=C(O)COC1=O
Reaction #5343
4-hydroxy-3-((Z)-1-oxo-9-hexadecenyl)-2(5H)-furanone
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCCCCCCC#CCCCCCCCC(=O)C1=C(O)COC1=O
Reaction #5344
4-hydroxy-3-(1-oxo-9-octadecynyl)-2(5H)-furanone
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCCCCCCCCCCCCCCCC(=O)C1=C(O)COC1=O
Reaction #5345
4-hydroxy-3-(1-oxooctadecyl)-2(5H)-furanone
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(CCCCCCCCOc1ccc(Cl)cc1)C1=C(O)COC1=O
Reaction #5346
3-[9-(4-chlorophenoxy)-1-oxononyl]4-hydroxy-2(5H)-furanone
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCCCCCc1ccc(OCCCCCC(=O)C2=C(O)COC2=O)cc1
Reaction #5347
3-[6-(4-heptylphenoxy)-1-oxohexyl]-4-hydroxy-2(5H)-furanone
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(CCCCCCCC=Cc1ccc(Cl)cc1)C1=C(O)COC1=O
Reaction #5355
4-hydroxy-3-[10-(4-chlorophenyl)-1-oxodec-9-enyl] -2(5H)-furanone
Ausbeute 58.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCCCCCCCCCCCCCC(=O)C1=C(O)COC1=O
Reaction #5367
4-hydroxy-3-[1-oxohexadecyl]-2(5H)-furanone
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(CCC1CCCCCCCCCCC1)C1=C(O)COC1=O
Reaction #65579
3-(3-Cyclododecyl-1-oxopropyl)-4-hydroxy-2(5H)-furanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
O=C(NCCC1CCCCCCCCCCC1)C1=C(O)COC1=O
Reaction #65588
4-Hydroxy-2-oxo-2.5-dihydro-furan-3-carboxylic acid-2-cyclododecyl-ethylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
O=C(CCC1CCCCC1)C1=C(O)COC1=O
Reaction #216718
3-(3-cyclohexyl-1-oxopropyl)-4-hydroxy-2(5H)-furanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
O=C(CCCC1CCCCC1)C1=C(O)COC1=O
Reaction #216719
3-(4-cyclohexyl-1-oxobutyl)-4-hydroxy-2(5H)-furanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
O=C(NCCC1CCCCCCCCCCC1)C1=C(O)COC1=O
Reaction #216721
4-Hydroxy-2-oxo-2,5-dihydro-furan-3-carboxylic acid-2-cyclododecyl-ethylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
O=C1OCC(O)=C1N=Nc1ccccc1
Reaction #319622
3-phenylazo-4-hydroxyfuran-2(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
CC(C)NC(=O)NC(C)C
Reaction #411106
diisopropyl urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
[N-]=[N+]=C1C(=O)COC1=O
Reaction #463545
title compound
Ausbeute 29.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
CCc1n[nH]c2ccc(C3C(C#N)=C(C)NC4=C3C(=O)OC4)cc12
Reaction #495728
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
Cc1n[nH]c2ccc(C3C(C#N)=C(C(F)(F)F)NC4=C3C(=O)OC4)cc12
Reaction #495737
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
O=C1C=C(N(Cc2ccc(Cl)nc2)CC(F)F)CO1
Reaction #512921
4-[[(6-chloropyridin-3-yl)methyl](2,2-difluoroethyl)amino]furan-2(5H)-one
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
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