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COc1ccc([C@@H]2CC(=O)c3c(O)cc(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)cc3O2)cc1O.[Ag]
Reaction #89803
Hesperidin silver
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(c2ccc(O)cc2)Oc2cc(O)cc(O)c21
Reaction #203809
DOI: 10.1039/C8SC04228D
COc1cc(OC2CCCCO2)cc(Br)c1C=O
Reaction #272393
DOI: 10.1039/C8SC04228D
COc1cc(OC2CCCCO2)cc(C)c1C=O
Reaction #294449
DOI: 10.1039/C8SC04228D
COc1ccc(CCC(=O)c2c(O)cc(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)cc2O)cc1O
Reaction #355344
neohesperidin dihydrochalcone
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CCC(=O)c2c(O)cc(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)cc2O)cc1O
Reaction #355345
neohesperidin dihydrochalcone
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1O[C@@H](O[C@H]2[C@H](Oc3cc(O)c(C(=O)CCc4ccc(O)cc4)c(O)c3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O
Reaction #458934
dihydrochalcone
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CCC(O)c2c(O)cc(O)cc2O)cc1O
Reaction #586161
1-(2,4,6-trihydroxyphenyl)-3-(3′-hydroxy-4′-methoxyphenyl)-1-propanol
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OC2CCCCO2)ccc(C=O)c1O
Reaction #675091
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C[C@@H](c2ccc(O)cc2)Oc2cc(O)cc(O)c21
Reaction #935898
naringenin
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC2CCCCO2)cc(C)c1CN1CCCCC1
Reaction #1021275
DOI: 10.1039/C8SC04228D
COc1ccc(CCC(O)c2c(O)cc(O)cc2O)cc1O
Reaction #1113370
1-(2,4,6-trihydroxyphenyl)-3-(3′-hydroxy-4′-methoxyphenyl)-1-propanol
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C=O)ccc(O)c1C
Reaction #1122396
52A
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(O[C@@H]2O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]2OC(C)=O)ccc1C=O
Reaction #1144005
2-methoxy-4-[(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl) oxy]benzaldehyde
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](O)[C@H](O)[C@@H](O)[C@@H](O)C=O
Reaction #1172416
L-rhamnose
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC2CCCCO2)ccc1CNc1ccc(OCCN2CCCC2)cc1
Reaction #1211466
DOI: 10.1039/C8SC04228D
COc1ccc([C@@H]2CC(=O)c3c(O)cc(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)cc3O2)cc1O
Reaction #1535017
hesperidin
DOI: 10.6084/m9.figshare.5104873.v1
CC1(O)c2ccc(OC3CCCCO3)cc2OC(c2ccc(I)cc2)C1c1ccc(OC2CCCCO2)cc1
Reaction #1561677
2-(4-iodophenyl)-4-methyl-7-((tetrahydro-2H-pyran-2-yl)oxy)-3-(4-((tetrahydro-2H-pyran-2-yl)oxy)phenyl)chroman-4-ol
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC2CCCCO2)cc(C)c1CN1CCCCC1
Reaction #1593074
title compound
Ausbeute 101.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@@H]2CC(=O)c3c(O)cc(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)cc3O2)cc1O
Reaction #1612325
hesperidin
DOI: 10.6084/m9.figshare.5104873.v1
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