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874522

CC1Cc2ccc(O)cc2C1=O
Reaction #65972
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccc(OC[C@H]3CCCO3)cc2CC1O
Reaction #156682
2-Hydroxy-5-[(R)-1-(tetrahydrofuran-2-yl)methoxy]-indan-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1Cc2cc(OC[C@H]3CCCO3)ccc2C1=O
Reaction #156683
Acetic acid 1-oxo-5-[(R)-1-(tetrahydrofuran-2-yl)methoxy]-indan-2-yl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)C12OC2c1ccccc1
Reaction #182831
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC(Oc2cc(Cl)ccc2OC2Cc3ccccc3C2=NO)C1
Reaction #324452
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)C12OC2c1ccc(Cl)c(Cl)c1
Reaction #404173
DOI: 10.1039/C8SC04228D
O=C(O)c1ccc(-c2n[nH]c3c2Cc2ccccc2-3)cc1
Reaction #466029
4-(1,4-dihydroindeno[1,2-c]pyrazol-3-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)ccc2c1CC(Oc1ccc([N+](=O)[O-])cc1)C2=O
Reaction #476503
desired product
Ausbeute 73.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)ccc2c1CC(Oc1ccc([N+](=O)[O-])cc1)C2
Reaction #476504
desired product
Ausbeute 70.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2ccc(O)cc2C1=O
Reaction #571423
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)C12OC2c1ccc(Cl)c(Cl)c1
Reaction #577969
3-(3,4-dichlorophenyl)-spiro (oxirane-2,2′-indan)-1′,3′-dione
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1cc(C)c(C)cc1C1(OC(C)=O)C(=O)c2ccccc2C1=O
Reaction #614288
title compound
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1cc(Cl)ccc1C1(OC(C)=O)C(=O)c2ccccc2C1=O
Reaction #614289
title compound
Ausbeute 19.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(C2(OC(C)=O)C(=O)c3ccccc3C2=O)c(OC(C)=O)c1
Reaction #614290
title compound
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1cc(-c2ccccc2)ccc1C1(OC(C)=O)C(=O)c2ccccc2C1=O
Reaction #614291
title compound
Ausbeute 11.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1ccc([N+](=O)[O-])cc1C1(OC(C)=O)C(=O)c2ccccc2C1=O
Reaction #614292
title compound
Ausbeute 11.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1ccc(OC(C)=O)c(C2(OC(C)=O)C(=O)c3ccccc3C2=O)c1
Reaction #614293
title compound
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(OC(C)=O)c(C2(OC(C)=O)C(=O)c3ccccc3C2=O)c1
Reaction #614294
title compound
Ausbeute 27.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)c1ccc(OC(C)=O)c(C2(OC(C)=O)C(=O)c3ccccc3C2=O)c1
Reaction #614295
title compound
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1ccc(C(C)(C)C)cc1C1(OC(C)=O)C(=O)c2ccccc2C1=O
Reaction #614296
title compound
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1
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