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CCOC(=O)CCCc1ccc(Br)cc1

CCOC(=O)CCCc1cccc(Br)c1
Reaction #1307
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCc1cccc(Br)c1
Reaction #1462
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCc1ccccc1)(CC(=O)c1ccc(Br)cc1)C(=O)OCC
Reaction #9619
diethyl 2-[2-(4-bromophenyl)-2-oxoethyl]-2-(2-phenylethyl)malonate
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCc1ccccc1)CC(=O)c1ccc(Br)cc1
Reaction #9620
ethyl 4-(4-bromophenyl)-4-oxo-2-(2-phenylethyl)butanoate
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCc1ccccc1)CC(=O)c1ccc(-c2ccc([N+](=O)[O-])cc2)cc1
Reaction #9621
ethyl 4-(4′-nitro-1,1′-biphenyl-4-yl)-4-oxo-2-(2-phenylethyl)butanoate
Ausbeute 75.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(CC(=O)c1ccc(Br)cc1)C(=O)OCC
Reaction #9623
ethyl 2-[2-(4-bromophenyl)-2-oxoethyl]pentanoate
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(CC(=O)c1ccc(-c2ccc([N+](=O)[O-])cc2)cc1)C(=O)OCC
Reaction #9624
ethyl 2-[2-(4′-nitro-1,1′-biphenyl-4-yl)-2-oxoethyl]pentanoate
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCOC)CC(=O)c1ccc(Br)cc1
Reaction #9625
ethyl 4-(4-bromophenyl)-2-(2-methoxyethyl)-4-oxobutanoate
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCOC)CC(=O)c1ccc(-c2ccc([N+](=O)[O-])cc2)cc1
Reaction #9626
ethyl 2-(2-methoxyethyl)-4-(4′-nitro-1,1′-biphenyl-4-yl)-4-oxobutanoate
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOC(=O)[C@@H]1CCCC[C@H]1C(=O)c1ccc(Br)cc1
Reaction #9636
trans-(trimethylsilyl)ethyl 2-(4-bromobenzoyl)cyclohexanecarboxylate
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2oc(Nc3ccc(-c4ccc(C(=O)[C@@H]5CCCC[C@H]5C(=O)OCC[Si](C)(C)C)cc4)cc3)nc2c1
Reaction #9715
trans-2-(trimethylsilyl)ethyl-2-({4′-[(5-methyl-1,3-benzoxazol-2-yl)amino]biphenyl-4-yl}carbonyl)cyclohexanecarboxylate
Ausbeute 50.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CC(=O)c1ccc(Br)cc1)C(C)=O
Reaction #46917
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(-c2ccc(Br)cc2)n(-c2ccc(S(N)(=O)=O)cc2)c1C
Reaction #46918
ethyl 1-[4-(aminosulfonyl)phenyl]-5-(4-bromophenyl)-2-methyl-1H-pyrrole-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCc1cccc(Br)c1
Reaction #52843
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCc1ccccc1)(CC(=O)c1ccc(Br)cc1)C(=O)OCC
Reaction #59113
diethyl 2-[2-(4-bromophenyl)-2-oxoethyl]-2-(2-phenylethyl)malonate
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCc1ccccc1)CC(=O)c1ccc(Br)cc1
Reaction #59114
ethyl 4-(4-bromophenyl)-4-oxo-2-(2-phenylethyl)butanoate
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCc1ccccc1)CC(=O)c1ccc(-c2ccc([N+](=O)[O-])cc2)cc1
Reaction #59115
ethyl 4-(4′-nitro-1,1′-biphenyl-4-yl)-4-oxo-2-(2-phenylethyl)butanoate
Ausbeute 75.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(CC(=O)c1ccc(Br)cc1)C(=O)OCC
Reaction #59117
ethyl 2-[2-(4-bromophenyl)-2-oxoethyl]pentanoate
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(CC(=O)c1ccc(-c2ccc([N+](=O)[O-])cc2)cc1)C(=O)OCC
Reaction #59118
ethyl 2-[2-(4′-nitro-1,1′-biphenyl-4-yl)-2-oxoethyl]pentanoate
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCOC)CC(=O)c1ccc(Br)cc1
Reaction #59119
ethyl 4-(4-bromophenyl)-2-(2-methoxyethyl)-4-oxobutanoate
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
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