Substructure Search

5481

COc1ccccc1N(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)C(=O)c1ccc(N)cc1
Reaction #2572
title compound
Yield 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
Yield 84.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1
Reaction #2583
title compound
Yield 95.6%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
Yield 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
Yield 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
Yield 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
Yield 77.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccc(O)c2)cc1
Reaction #2612
title compound
Yield 76.7%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1.NC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1.O=C(O)/C=C/C(=O)O
Reaction #2630
title compound
Yield 56.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(N2CCN(C(=O)c3cc(C#N)ccc3N3CCOCC3)CC2)c(F)c1
Reaction #61002
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Cc1ccc(C(C)(CCCCC(=O)CCCCC(C)(C(=O)O)c2ccc(CC(C)C)cc2)C(=O)O)cc1
Reaction #76265
2,12-bis-(4-isobutyl-phenyl)-2,12-dimethyl-7-oxo-tridecanedioic acid
Yield 86.2%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc(C2C=C(C(F)(F)F)NC3=C2C(=O)CCC3)c1
Reaction #82736
title compound
Yield 55.2%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc(C2C=C(C(F)(F)F)NC3=C2C(=O)CCC3)c1
Reaction #82739
title compound
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #84822
foam
Yield 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cc(-c2ccc(F)cc2F)cc(-n2cnc3cc(-c4cnc(N)s4)ccc32)c1
Reaction #92432
crude residue
Yield 14.7%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(=O)CC(C)(C)P1c1ccccc1-c1ccccc1
Reaction #166163
title compound
Yield 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1ccc(C2(C(=O)Nc3ccc(N4CCC(NCC(C)=O)C4)cc3)CC2)cc1
Reaction #173250
DOI: 10.1039/C8SC04228D
CCCC(=O)c1cnc2c(C(O)CN(C)C)cccc2c1Nc1ccccc1C
Reaction #173902
DOI: 10.1039/C8SC04228D
CC(=O)c1ccc(Nc2nc3ccc(C(=O)N(CCC(C)C)CCC(C)C)cc3n2CCC=O)cc1
Reaction #177181
DOI: 10.1039/C8SC04228D
CC(=O)c1ccc(OCc2ccc(Cc3cccc(-c4nn[nH]n4)c3)cc2)c(C(C)C)c1O
Reaction #189991
DOI: 10.1039/C8SC04228D
Page 1Next