coumarin

C=Cc1ccccc1O
Reaction #174714
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCC(=O)Oc1cc2oc(=O)c(C(=O)NCC(=O)O)cc2cc1Cl
Reaction #385976
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCN=[N+]=[N-]
Reaction #400851
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=c1ccc2cc([N+](=O)[O-])ccc2o1
Reaction #468394
6-nitrocoumarin
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
—
Reaction #610523
adduct
Ausbeute 92.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1cc(=O)oc2cc(OC(=O)c3ccccc3)ccc12
Reaction #644333
7-benzoyloxy-4-methyl-coumarin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
O=C1Oc2ccccc2C2CN(Cc3ccccc3)CC12
Reaction #645111
desired product
Ausbeute 70.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
CCCC(=O)Oc1cc2oc(=O)c(C(=O)NCC(=O)O)cc2cc1Cl
Reaction #705980
7-Butyryloxy-3-carboxymethylaminocarbonyl-6-chlorocoumarin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_09
Nc1cc2ccccc2oc1=O.c1ccncc1
Reaction #955147
pyridine aminocoumarin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_10
F[P-](F)(F)(F)(F)F
Reaction #1031384
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
O=C1Oc2ccccc2C2CN(Cc3ccccc3)CC12
Reaction #1056375
desired product
Ausbeute 70.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_12
CCCC(=O)Oc1cc2oc(=O)c(C(=O)NCC(=O)O)cc2cc1Cl
Reaction #1080017
7-Butyryloxy-3-carboxymethylaminocarbonyl-6-chlorocoumarin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_10
CCCCCCCCCCCCCCCCC=O
Reaction #1108148
heptadecanal
Ausbeute 21.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_05
O=S(=O)([O-])C(F)(F)F.O=c1ccc2ccc([S+](c3ccccc3)c3ccccc3)cc2o1
Reaction #1259210
diphenyl(coumarin-7-yl)sulfonium trifluoromethanesulfonate
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_11
F[P-](F)(F)(F)(F)F.O=c1ccc2ccc([I+]c3ccccc3)cc2o1
Reaction #1259213
crystal
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_11
O=C(Cc1cc(=O)oc2cc(OC3OC(CO)C(O)C(O)C3O)ccc12)NCCO
Reaction #1313987
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CCCC(=O)Oc1cc2oc(=O)c(C(=O)NCC(=O)O)cc2cc1Cl
Reaction #1328409
7-Butyryloxy-3-carboxymethylaminocarbonyl-6-chlorocoumarin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_10
O=C1CCc2ccccc2O1
Reaction #1349756
dihydrocoumarin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_06
CCCC(=O)Oc1cc2oc(=O)c(C(=O)NCC(=O)O)cc2cc1Cl
Reaction #1445360
7-Butyryloxy-3-carboxymethylaminocarbonyl-6-chlorocoumarin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_07
COc1ccc(C(=O)Nc2cc3ccc(O[C@@H]4OC(C)(C)[C@H](OC)[C@@H](O)[C@H]4O)c(C)c3oc2=O)cc1-c1ccccc1
Reaction #1598432
28
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_07
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