Busqueda de Subestructura

COCOc1ccc(C=O)cc1

COCCOCOc1ccc(C(O)C(=O)O)c(Cl)c1OCOCCOC
Reaction #2669
[2-chloro-3,4-bis-[(2-methoxy-ethoxy)-methoxy]-phenyl]-hydroxy acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OCc2cc(C(=O)CBr)ccc2O1
Reaction #5306
title compound
Rendimiento 82.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(OC2CCCCO2)cc1
Reaction #7427
p-tetrahydropyranyloxy benzoic acid
Rendimiento 86.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(OCOC)c(C2CCCN2C(=O)OC(C)(C)C)c1
Reaction #41539
t-butyl 2-(5-ethoxycarbonyl-2-methoxymethoxy-phenyl)-pyrrolidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(O)c(C2CCCN2C(C)=O)c1
Reaction #41540
compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc2c(c1)COC(C)(C)O2
Reaction #42731
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OCc2cc(C(=O)CBr)ccc2O1
Reaction #42732
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OCc2cc([C@@H](O)CBr)ccc2O1
Reaction #42733
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(C=Cc1cccc(Br)c1)c1ccc(OC2CCCCO2)cc1
Reaction #44817
powder
Rendimiento 55.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C=Cc1cccc(Cl)c1Cl)c1ccc(OC2CCCCO2)cc1
Reaction #44818
powder
Rendimiento 87.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2c(c1)C(F)(F)OC(F)(F)O2
Reaction #46217
2,2,4,4-tetrafluoro-4H-benzo[1,3]dioxine-6-carboxylic acid methyl ester
Rendimiento 169.8%DOI: 10.6084/m9.figshare.5104873.v1
OCc1ccc2c(c1)C(F)(F)OC(F)(F)O2
Reaction #46218
(2,2,4,4-tetrafluoro-4H-benzo[1,3]dioxin-6-yl)-methanol
Rendimiento 96.8%DOI: 10.6084/m9.figshare.5104873.v1
COCOc1ccc2c(c1Cl)C(O)N(C(C)(C)c1ccccc1)C2=O
Reaction #49536
4-chloro-5-methoxymethoxy-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinone
Rendimiento 98.1%DOI: 10.6084/m9.figshare.5104873.v1
COCOc1cc(I)c2c(c1Cl)C(O)N(C(C)(C)c1ccccc1)C2=O
Reaction #49537
4-chloro-5-methoxymethoxy-3-hydroxy-7-iodo-2-(1-methyl-1-phenylethyl)isoindolinone
Rendimiento 96.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(c1ccccc1)N1Cc2c(Cl)c(O)cc(I)c2C1=O
Reaction #49538
4-chloro-5-hydroxy-7-iodo-2-(1-methyl-1-phenylethyl)isoindolinone
Rendimiento 108.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(OC2CCCCO2)cc1F
Reaction #58887
desired product
Rendimiento 74.0%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
O=C(CC(=O)c1snc(Cl)c1Cl)c1ccc(O)cc1
Reaction #77686
1-(3,4-dichloro-5-isothiazolyl)-3-(4-hydroxyphenyl)-1,3-propanedione
Rendimiento 88.8%DOI: 10.6084/m9.figshare.5104873.v1
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