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CC(=O)C(C)C

COc1ccccc1N(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)C(=O)c1ccc(N)cc1
Reaction #2572
title compound
Выход 98.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1N(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)C(=O)c1ccc(NC(C)=O)cc1
Reaction #2573
title compound
Выход 84.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccc(C)c2)cc1
Reaction #2579
title compound
Выход 100.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)C(=O)c2ccccc2NC(C)=O)c1
Reaction #2584
title compound
Выход 65.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2ccccc2)c1
Reaction #2589
title compound
Выход 74.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2ccc(C)cc2)c1
Reaction #2590
title compound
Выход 97.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2ccc(F)cc2)c1
Reaction #2591
title compound
Выход 98.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cc(C)cc(C)c2)cc1
Reaction #2594
title compound
Выход 86.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1N(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)C(=O)c1ccc(NC(=O)C(C)(C)C)cc1
Reaction #2599
title compound
Выход 91.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1N(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)C(=O)c1ccc(NS(C)(=O)=O)cc1
Reaction #2601
title compound
Выход 50.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2ccccc2OC)cc1
Reaction #2604
title compound
Выход 37.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1N(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)C(=O)c1ccc(NC(=O)NC(C)(C)C)cc1
Reaction #2607
title compound
Выход 77.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1.CCCCC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1.O=C(O)/C=C/C(=O)O
Reaction #2626
title compound
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC=CCOc1ccc(C)c2c1C(=O)C(C)C2c1ccccc1
Reaction #5090
2,3-dihydro-2,4-dimethyl-3-phenyl-7-crotyloxy-1H-inden-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(=O)C(=Cc1ccccc1)C(=O)Nc1ccccc1
Reaction #5780
4-methyl-3-oxo-N-phenyl-2-(phenylmethylene)pentanamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(=O)C(=Cc1ccccc1)C(=O)Nc1ccccc1
Reaction #5786
4-methyl-3-oxo-N-phenyl-2-(phenylmethylene)pentanamide
Выход 84.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(=O)CC(=O)Nc1ccccc1
Reaction #5813
4-methyl-3-oxo-N-phenylpentanamide
Выход 157.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(=O)CC(=O)Nc1ccccc1
Reaction #6559
4-methyl-3-oxo-N-phenylpentanamide
Выход 157.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(Br)cc1)[C@H]1C[C@H]1C(=O)O
Reaction #9637
cis-2-(4-bromobenzoyl)cyclopropanecarboxylic acid
Выход 74.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@@H]1C(=O)c1ccc(Br)cc1
Reaction #9638
methyl cis-2-(4-bromobenzoyl)-cyclopropanecarboxylate
Выход 99.7%DOI: 10.6084/m9.figshare.5104873.v1
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