Impliqué dans 591 réactions

5137

COc1ccc2c(c1)CCc1c-2c(=O)oc2cc(O)ccc12
Reaction #1805
title compound
Rendement 70.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CC=C1c2ccc(O)cc2Oc2cc(O)ccc21
Reaction #4977
powder
Rendement 88.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOCC.Oc1cccc(O)c1
Reaction #5383
resorcinol ether
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Oc1cccc(OCCCCOc2cccc(O)c2)c1
Reaction #5630
1,4-BIS(3-HYDROXYPHENOXY)BUTANE
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Oc1cccc(OCCCCCCCCOc2cccc(O)c2)c1
Reaction #5633
product
Rendement 27.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(Cc1ccc(Cl)cc1)c1ccc(O)cc1O
Reaction #42772
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=c1cc(CCl)c2ccc(O)cc2o1
Reaction #43923
title compound
Rendement 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #46938
phenols
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCC(=O)c1ccc(O)cc1O
Reaction #49846
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
O=c1cc(-c2ccoc2)c2ccc(O)cc2o1
Reaction #49847
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
O=c1cc(-c2ccccc2)c2ccc(O)cc2o1
Reaction #49849
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
Oc1cc(O)c(C23CC4CC(CC(C4)C2)C3)cc1C12CC3CC(CC(C3)C1)C2
Reaction #51281
product
Rendement 66.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Oc1ccc(-c2nc(-c3ccc(Oc4ccccc4)cc3)nc(-c3ccc(Oc4ccccc4)cc3)n2)c(O)c1
Reaction #52127
2-(2,4-dihydroxyphenyl)-4,6-bis(4-phenoxyphenyl)-1,3,5-triazine
Rendement 74.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Oc1ccc(-c2nc(-c3ccc(Oc4ccccc4)cc3)nc(-c3ccc(O)cc3O)n2)c(O)c1
Reaction #52131
2,4-bis(2,4-dihyroxyphenyl)-6-(4-phenoxyphenyl)-1,3,5-triazine
Rendement 10.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCC1(C)C=C(c2cccc(C(F)(F)F)c2)c2ccc(O)cc2O1
Reaction #54570
chromene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
O=C1CC(c2cccc3ccccc23)c2ccc(O)cc2O1
Reaction #54571
dihydrocoumarin
Rendement 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
COc1ccc2cc(-c3cc(=O)oc4cc(O)ccc34)ccc2c1
Reaction #54575
7-hydroxy-4(6-methoxy-2-naphthyl)coumarin
Rendement 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
O=c1cc(-c2ccc3ccccc3c2)c2ccc(O)cc2o1
Reaction #54577
7-hydroxy-4-(2-naphthyl)coumarin
Rendement 26.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
Cc1cc(=O)oc2cc(O)ccc12
Reaction #54974
4-methyl-7-hydroxy-coumarin
Rendement 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CCOC(=O)c1cc(=O)oc2cc(O)ccc12
Reaction #54975
4-Carbethoxy-7-hydroxy-coumarin
Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
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