部分構造検索

CC(=O)c1ccc2c(c1)CC(C)O2

CC1Cc2cc(C(=O)O)ccc2O1
Reaction #3155
5-carboxy-2-methylcoumaran
収率 57.4%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@H]1Cc2c(ccc3c2O[C@@H]2COc4cc(OC)c(OC)cc4[C@@H]2C3=O)O1
Reaction #71312
rotenone
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@H]1/C=C/O[C@@]2(C)Oc3c(C)c(O)c4c(O)c(c(/C=N/N5CCN(C)CC5)c(O)c4c3C2=O)NC(=O)/C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C
Reaction #74993
rifampicin
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@H]1/C=C/O[C@@]2(C)Oc3c(C)c(O)c4c(O)c(c(/C=N/N5CCN(C)CC5)c(O)c4c3C2=O)NC(=O)/C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C
Reaction #74994
rifampicin
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@H]1/C=C/O[C@@]2(C)Oc3c(C)c(O)c4c(O)c(c(/C=N/N5CCN(C)CC5)c(O)c4c3C2=O)NC(=O)/C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C
Reaction #74995
rifampicin
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Cc2cc(C(=NN)c3ccc(Cl)cc3)ccc2O1
Reaction #189732
DOI: 10.1039/C8SC04228D
CCC1(C(=O)OC)Cc2cc(O)ccc2O1
Reaction #202005
DOI: 10.1039/C8SC04228D
CC12CCC(C1)C1(C)Oc3ccc(C(=O)c4ccc(C(=O)O)cc4)cc3C21C
Reaction #259413
DOI: 10.1039/C8SC04228D
O=C(c1ccc([N+](=O)[O-])cc1)c1cc2c(c(Cl)c1Cl)OC(C(=O)O)C2
Reaction #295928
DOI: 10.1039/C8SC04228D
O=C(c1ccco1)c1cc2c(c(Cl)c1Cl)OC(C(=O)O)C2
Reaction #348211
(±)6,7-Dichloro-2,3-dihydro-5-(2-furoyl)benzofuran-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(N)c1ccccc1
Reaction #348213
(+)-α-methylbenzylamine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cccs1)c1cc2c(c(Cl)c1Cl)OC(C(=O)O)C2
Reaction #349571
6,7-Dichloro-2,3-dihydro-5-(2-thenoyl)benzofuran-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc2cc(C(=O)c3cccs3)c(Cl)c(Cl)c2o1
Reaction #349572
methyl 6,7-dichloro-5-(2-thenoyl)benzofuran-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccco1)c1cc2c(c(Cl)c1Cl)OC(C(=O)O)C2
Reaction #349573
6,7-Dichloro-2,3-dihydro-5-(2-furoyl)-benzofuran-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCC=C1Cc2c3c(c(C)c(C)c2C1=O)OC(C(=O)O)C3
Reaction #407034
DOI: 10.1039/C8SC04228D
CC1(C)Cc2cc(C(=O)c3ccc(OS(=O)(=O)C(F)(F)F)cc3)ccc2O1
Reaction #417506
(4-trifluoromethylsulfonyloxyphenyl)(2,3-dihydro-2,2-dimethylbenzofuran-5-yl) ketone
収率 77.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Cc2cc(C(=NN)c3ccc(OS(=O)(=O)C(F)(F)F)cc3)ccc2O1
Reaction #417507
(4-trifluoromethylsulfonyloxyphenyl)(2,3-dihydro-2,2-dimethylbenzofuran-5-yl) ketone hydrazone
収率 96.5%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Cc2cc(C(=NN)c3ccc(Cl)cc3)ccc2O1
Reaction #417508
(4-chlorophenyl) (2,3-dihydro-2,2-dimethylbenzofuran-5-yl) ketone hydrazone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cccs1)c1cc2c(c(Cl)c1Cl)OC(C(=O)O)C2
Reaction #458916
(±)6,7-Dichloro-2,3-dihydro-5-(2-thenoyl)benzofuran-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccco1)c1cc2c(c(Cl)c1Cl)OC(C(=O)O)C2
Reaction #458917
(±)6,7-Dichloro-2,3-dihydro-5-(2-furoyl)benzofuran-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
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