Recherche de Sous-structure

1091895

CCOC(=O)C1Nc2cc(Cl)cc(Cl)c2C2C=CCC12
Reaction #75639
Compound 1
Rendement 89.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1Nc2cc(Cl)cc(Cl)c2C2C=CCC12
Reaction #75640
7,9-dichloro-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinoline-4-carboxylic Acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Nc2ccc(Cl)cc2C2C=CCC12
Reaction #75641
Compound 3
Rendement 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Nc2cc(Cl)cc(Cl)c2C2c3ccccc3CCC12
Reaction #75646
Compound 12
Rendement 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Nc2cc(Cl)cc(Cl)c2C(c2ccccc2)C1C
Reaction #75674
Compound 42
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Nc2cc(Cl)cc(Cl)c2C(c2ccc(OC)cc2)C1c1ccccc1
Reaction #75675
Compound 43
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Nc2cc(Cl)cc(Cl)c2C(c2ccc(OC)cc2)C1c1ccc(OC)cc1
Reaction #75676
Compound 44
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Nc2cc(Cl)cc(Cl)c2C(c2ccc(OC)cc2)C1C
Reaction #75677
Compound 45
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Nc2cc(Cl)cc(Cl)c2C(c2ccc(OC)c(OC)c2)C1C
Reaction #75678
Compound 46
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Nc2cc(Cl)cc(Cl)c2C(c2cc(OC)c(OC)cc2OC)C1C
Reaction #75679
Compound 47
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Nc2cc(Cl)cc(Cl)c2C2CCCC12
Reaction #75690
Compound 59
Rendement 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Nc2ccccc2C2c3ccccc3CC12
Reaction #75691
Compound 61
Rendement 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Nc2ccc(OC(F)(F)F)cc2C2CCCCCCC12
Reaction #75698
Compound 76
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1Nc2ccccc2C[C@@H]1C
Reaction #80793
cis-2-methoxycarbonyl-3-methyltetrahydroquinoline
Rendement 78.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1Nc2ccccc2C[C@@H]1C
Reaction #80794
cis-2-methoxycarbonyl-3-methyltetrahydroquinoline
Rendement 47.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1Nc2cc(Cl)cc(Cl)c2C2C=CCC12
Reaction #264177
DOI: 10.1039/C8SC04228D
CCOC(=O)[C@H]1Nc2ccccc2[C@H]2[C@@H]1CCN2C(=O)OC(C)(C)C
Reaction #637436
title compound
Rendement 46.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC[C@@H]2[C@H](CO)Nc3ccccc3[C@@H]21
Reaction #637437
title compound
Rendement 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Nc2ccc(OC(F)(F)F)cc2C2CCCCCCC12
Reaction #769860
DOI: 10.1039/C8SC04228D
CCOC(=O)[C@H]1Nc2ccccc2[C@H]2[C@@H]1CCN2C(=O)OC(C)(C)C
Reaction #822899
title compound
Rendement 46.3%DOI: 10.6084/m9.figshare.5104873.v1
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