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1073058

COc1ccccc1[C@@H]1CN(Cc2ccccc2)C[C@H]1CO
Reaction #1166
expected product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(C)NC(CC)=C(C(=O)OCC)C1c1cc([N+](=O)[O-])ccc1OCCCCN
Reaction #4757
diethyl 4-[2-(4-aminobutoxy)-5-nitrophenyl]-2-ethyl-6-methyl-1,4-dihydropyridine-3,5-dicarboxylate
Ausbeute 65.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=C(C)NC(C)=C(C(=O)OC)C1c1cc([N+](=O)[O-])ccc1OCCCCNCC(O)COc1ccccc1
Reaction #4759
dimethyl 4-[2-[4-(2-hydroxy-3-phenoxypropylamino)butoxy]-5-nitrophenyl]-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate
Ausbeute 51.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(C)NC(CC)=C(C(=O)OCC)C1c1cc([N+](=O)[O-])ccc1OCCCCNCC(O)COc1ccccc1
Reaction #4763
diethyl 2-ethyl-4-[2-[4-(2-hydroxy-3-phenoxypropylamino)butoxy]-5-nitrophenyl]-6-methyl-1,4-dihydropyridine-3,5-dicarboxylate
Ausbeute 20.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(N)Cc1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11794
title compound
Ausbeute 100.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1CC(N)C(=O)O
Reaction #11795
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCSCCOc1cc(C)c(-c2cccc(COc3ccc4c(c3)OC[C@H]4CC(=O)OC)c2)c(C)c1
Reaction #43918
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)cc(OCCCS(C)(=O)=O)cc4COC(C)=O)c3)ccc21
Reaction #43930
title compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)cc(OC5CCS(=O)(=O)CC5)cc4C)c3)ccc21
Reaction #43943
title compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)c(C)c(OCCCS(C)(=O)=O)c(C)c4C)c3)ccc21
Reaction #43946
title compound
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)cc(OCCCS(C)(=O)=O)cc4C)c3)ccc21
Reaction #43948
title compound
Ausbeute 82.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)cc(OCCCS(C)(=O)=O)c(F)c4C)c3)ccc21
Reaction #43951
title compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H]1COc2cc(O)ccc21
Reaction #43957
Methyl[(3S)-6-hydroxy-2,3-dihydro-1-benzofuran-3-yl]acetate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)c(Cl)c(OCCCS(C)(=O)=O)c(Cl)c4C)c3)ccc21
Reaction #43960
title compound
Ausbeute 89.8%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(OCCCS(C)(=O)=O)cc(CC)c1-c1cccc(COc2ccc3c(c2)OC[C@H]3CC(=O)OC)c1
Reaction #43962
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(=O)c1cc(Cl)ccc1OC
Reaction #56832
3-(5-chloro-2-methoxy-phenyl)-3-oxopropionic acid ethyl ester
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1-c1cc(=O)[nH]c(C)n1
Reaction #56833
6-(5-chloro-2-methoxy-phenyl)-2-methyl-3H-pyrimidin-4-one
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C[C@@H]1COc2cc(OCc3cccnc3SC3CCCC3)ccc21
Reaction #91237
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(=O)c1cc(Cl)ccc1OC
Reaction #162713
title compound
Ausbeute 76.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C(\NCC(N)=O)c1cc(Cl)ccc1OC
Reaction #162714
title compound
Ausbeute 105.4%DOI: 10.6084/m9.figshare.5104873.v1
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