部分構造検索

1276954

O=c1cc(O)c2ccc(O)cc2o1
Reaction #1816
4,7-Dihydroxy-coumarin
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(O)c2ccc(O)cc2o1
Reaction #1819
4,7-Dihydroxy-coumarin
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(O)cc(=O)oc2c1OC1CCCC1
Reaction #48904
8-(cyclopentyloxy)-4-hydroxy-7-methoxy-2H-chromen-2-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(OS(=O)(=O)c3ccc(C)cc3)cc(=O)oc2c1OC1CCCC1
Reaction #48905
8-(cyclopentyloxy)-7-methoxy-2-oxo-2H-chromen-4-yl 4-methylbenzenesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(N)cc(=O)oc2c1OC1CCCC1
Reaction #48908
4-amino-8-(cyclopentyloxy)-7-methoxy-2H-chromen-2-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(Cl)cc(=O)oc2c1OC1CCCC1
Reaction #48912
4-chloro-8-(cyclopentyloxy)-7-methoxy-2H-chromen-2-one
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(=O)oc2ccccc12
Reaction #54315
4-aminocoumarin
収率 99.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(OC(F)(F)F)cc1)c1c(O)c2ccccc2oc1=O
Reaction #63545
4-hydroxy-3-(4-trifluoromethyloxyphenyl-carbamoyl)-coumarin
収率 45.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C=Cc1ccc(OC(F)(F)F)c(Cl)c1)c1c(O)c2ccccc2oc1=O
Reaction #66579
4-hydroxy-3-[3-[3-chloro-4-(trifluoromethoxy)phenyl]-1-oxo-2-propenyl]-2H-1-benzopyran-2-one
収率 36.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)c2c(Cc3c(S(=O)(=O)c4ccc(C)cc4)c4ccccc4oc3=O)c(=O)oc3ccccc23)cc1
Reaction #76808
3,3′-methylenebis[4-tosylcoumarin]
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(O)ccc2c(O)c(C(=O)Nc3cccc(F)c3)c(=O)oc12
Reaction #83610
title product
収率 27.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1C(F)(F)F)c1c(O)c2ccccc2oc1=O
Reaction #83611
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OCc2ccccc2)ccc2c(O)c(C(=O)Nc3cccc(Br)c3)c(=O)oc12
Reaction #83612
title compound
収率 15.2%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)NCCCOc1cc(=O)oc2ccc(Cl)cc12
Reaction #174604
DOI: 10.1039/C8SC04228D
COCCOC(=O)Nc1cccc(C=CC(=O)c2c(O)c3ccccc3oc2=O)c1
Reaction #178874
DOI: 10.1039/C8SC04228D
CCCc1c(OCC(O)COc2ccc3c(O)cc(=O)oc3c2)ccc(C(C)=O)c1O
Reaction #187348
DOI: 10.1039/C8SC04228D
CN(C)CCCOc1c(-c2ccccc2)c(=O)oc2ccccc12
Reaction #196070
DOI: 10.1039/C8SC04228D
O=c1oc2cc(O)ccc2c(OCCN2CCOCC2)c1-c1ccccc1
Reaction #207360
DOI: 10.1039/C8SC04228D
CCOC1Oc2c(c(=O)oc3ccc(C)cc23)C1c1c(O)c2cc(C)ccc2oc1=O
Reaction #218841
title compound
収率 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COC1Oc2c(c(=O)oc3cc(O)cc(C)c23)C1c1c(O)c2c(C)cc(O)cc2oc1=O
Reaction #218842
title compound
収率 92.0%DOI: 10.6084/m9.figshare.5104873.v1
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