4′,7-Dihydroxyisoflav-3-ene

Oc1ccc(C2=Cc3cc4c(cc3OC2)OCN(Cc2ccccc2)C4)cc1
Reaction #470410
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CC(c1ccccc1)N1COc2cc3c(cc2C1)C=C(c1ccc(O)cc1)CO3
Reaction #470411
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CCCN1COc2cc3c(cc2C1)C=C(c1ccc(O)cc1)CO3
Reaction #470412
title compound
Yield 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CN1COc2cc3c(cc2C1)C=C(c1ccc(O)cc1)CO3
Reaction #470413
title compound
Yield 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
Oc1ccc(C2=Cc3cc4c(cc3OC2)OCN(c2ccccc2)C4)cc1
Reaction #470414
title compound
Yield 7.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
Oc1ccc(C2=Cc3cc4c(cc3OC2)OCN(c2ccc(O)cc2)C4)cc1
Reaction #470415
title compound
Yield 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
Oc1ccc(C2=Cc3cc4c(cc3OC2)OCN(Cc2ccc(Cl)cc2)C4)cc1
Reaction #470419
title compound
Yield 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
Cc1ccc(N2COc3cc4c(cc3C2)C=C(c2ccc(O)cc2)CO4)cc1
Reaction #470420
title compound
Yield 22.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
Cc1cccc(N2COc3cc4c(cc3C2)C=C(c2ccc(O)cc2)CO4)c1
Reaction #470422
title compound
Yield 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
O=[N+]([O-])c1cccc(N2COc3cc4c(cc3C2)C=C(c2ccc(O)cc2)CO4)c1
Reaction #470423
title compound
Yield 4.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CC(C)(C)c1ccc(N2COc3cc4c(cc3C2)C=C(c2ccc(O)cc2)CO4)cc1
Reaction #470425
title compound
Yield 15.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
Oc1ccc(C2=Cc3cc4c(cc3OC2)OCN(Cc2cccc3ccccc23)C4)cc1
Reaction #470426
title compound
Yield 38.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
Cc1ccc(N2COc3cc4c(cc3C2)C=C(c2ccc(O)cc2)CO4)cc1C
Reaction #470427
title compound
Yield 21.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
Oc1cccc(C2=Cc3ccc(O)cc3OC2)c1
Reaction #690463
Isoflav-3-ene-3′,7-diol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
COc1cccc(C2=Cc3ccc(O)cc3OC2)c1
Reaction #690464
3′-MethoxyIsoflav-3-ene-7-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
Oc1ccc2c(c1)OCC(c1ccccc1)=C2
Reaction #690465
Isoflav-3-ene-7-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
Oc1ccc(C2COc3cc(O)ccc3C2)cc1
Reaction #1978612
3-(4-Hydroxy-phenyl)-chroman-7-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_08
Oc1ccc(C2COc3cc(O)ccc3C2)cc1
Reaction #2420909
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (10/10)