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4046

Cc1ccc(OC(=CC(=O)c2ccc(Br)cc2)C(=O)c2ccc(Br)cc2)cc1
Reaction #887
1-(4-tolyloxyl)-1,2-bis(4-bromobenzoyl)ethylene
DOI: 10.6084/m9.figshare.5104873.v1
COC(CC(=O)c1ccc(Br)cc1)C(=O)c1ccc(Br)cc1
Reaction #889
1,2-Bis(4-bromobenzoyl)-1-methoxyethane
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(-c2ccc([C@H]3CC[C@H](O)CC3)cc2)cc1
Reaction #5398
trans-4-(4'-cyano-4-biphenylyl)cyclohexanol
Ausbeute 34.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCC/C=C\C[C@H]1C(=O)C[C@@H](O)[C@@H]1c1ccc2c(c1)CCC2O
Reaction #9339
15-6
Ausbeute 434.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCC/C=C\C[C@H]1C(=O)C[C@@H](O)[C@@H]1c1ccc2c(c1)CCC2=O
Reaction #9340
15-8
Ausbeute 64.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H]1C[C@H]1C(=O)c1ccc(Br)cc1
Reaction #9639
trans-2-(4-bromobenzoyl)cyclopropanecarboxylic acid
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H]1C(=O)c1ccc(Br)cc1
Reaction #9640
methyl trans-2-(4-bromobenzoyl)cyclopropanecarboxylate
Ausbeute 83.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H]1C[C@H]1C(=O)c1ccc(Br)cc1
Reaction #59136
trans-2-(4-bromobenzoyl)cyclopropanecarboxylic acid
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H]1C(=O)c1ccc(Br)cc1
Reaction #59137
methyl trans-2-(4-bromobenzoyl)cyclopropanecarboxylate
Ausbeute 83.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1C(=O)Nc2ccc(Cl)cc2CC1c1ccc(OC)cc1
Reaction #63800
title compound
Ausbeute 91.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(=O)CC(O)(Cc1ccccc1)C(=O)O
Reaction #70129
4-phenylmethyl-4-hydroxy-2-oxoglutaric acid
DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc(-c2cc(-c3ccccc3)c(-c3ccccc3)s2)cc1
Reaction #74936
2,3-diphenyl-5-p-bromophenylthiophene
Ausbeute 117.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CC(c2ccccc2)c2c(Cl)cc(Cl)cc2N1
Reaction #75648
Compound 15
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(C2CC(C(=O)O)Nc3cc(Cl)cc(Cl)c32)c1
Reaction #75650
Compound 18
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CC(c2ccc(F)cc2)c2c(Cl)cc(Cl)cc2N1
Reaction #75663
Compound 31
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(c2ccc(Br)cc2)c2c(Cl)cc(Cl)cc2N1
Reaction #75671
Compound 39
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CC(c2ccc(Br)cc2)c2c(Cl)cc(Cl)cc2N1
Reaction #75672
Compound 40
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(c2ccccc2Cl)c2cc(Cl)ccc2N1
Reaction #75684
Compound 52
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Nc2ccccc2C2c3ccccc3CC12
Reaction #75691
Compound 61
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cc(C(=O)N[C@@H](CC(=O)O)Cc2ccccc2)nn1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #158836
title compound
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
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