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523087

C=C1CCCCCCCCCCC(C(=O)O)NC1=O
Reaction #5508
3-methylidene-2-oxo-1-azacyclotetradecane-14-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CC1CC2CCC1C2)N1CC(Oc2c(F)cccc2F)=CC1=O
Reaction #47633
3-bicyclo[2.2.1]hept-2-yl-2-[4-(2,6-difluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid methyl ester
المردود 21.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(CC1CC2CCC1C2)N1CC(Oc2c(F)cccc2F)=CC1=O
Reaction #47634
3-bicyclo[2.2.1]hept-2-yl-2-[4-(2,6-difluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid
المردود 87.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)Cn1ccc(NC(=O)C(CC2CC3CCC2C3)N2CC(Oc3c(F)cccc3F)=CC2=O)n1
Reaction #47635
3-bicyclo[2.2.1]hept-2-yl-2-[4-(2,6-difluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-N-[1-(2-hydroxy-2-methyl-propyl)-1H-pyrazol-3-yl]-propionamide
المردود 40.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CC1C2CCC1CC2)N1CC(Oc2ccccc2Cl)=CC1=O
Reaction #47642
3-bicyclo[2.2.1]hept-7-yl-2-[4-(2-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid methyl ester
المردود 47.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(CC1C2CCC1CC2)N1CC(Oc2ccccc2Cl)=CC1=O
Reaction #47643
3-bicyclo[2.2.1]hept-7-yl-2-[4-(2-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid
المردود 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)Cn1ccc(NC(=O)C(CC2C3CCC2CC3)N2CC(Oc3ccccc3Cl)=CC2=O)n1
Reaction #47644
3-bicyclo[2.2.1]hept-7-yl-2-[4-(2-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-N-[1-(2-hydroxy-2-methyl-propyl)-1H-pyrazol-3-yl]-propionamide
المردود 61.9%DOI: 10.6084/m9.figshare.5104873.v1
C=C1CCCCCCCCCCC(C(=O)O)NC1=O
Reaction #50263
3-methylidene-2-oxo-1-azacyclotetradecane-14-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCC(C)NC(=O)C=C(c1ccccc1)c1ccc([N+](=O)[O-])cc1
Reaction #94898
title compound
المردود 51.0%DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #94899
oil
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCC(C)NC(=O)C=C(c1ccccc1)c1ccc(N)cc1
Reaction #94902
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCC(C)NC(=O)C=C(c1ccccc1)c1cccc(N)c1
Reaction #94903
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCC(C)NC(=O)C=Cc1cccc([N+](=O)[O-])c1
Reaction #95086
title product
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCC(C)NC(=O)C=C(C)c1cccc([N+](=O)[O-])c1
Reaction #95088
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCC(C)NC(=O)C=C(C)c1cccc([N+](=O)[O-])c1
Reaction #95089
title product
المردود 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCC(C)NC(=O)C=C(C)c1cccc(N)c1
Reaction #95091
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCC(C)NC(=O)C=C(C)c1cccc([N+](=O)[O-])c1
Reaction #185277
DOI: 10.1039/C8SC04228D
CCCCCCCCCC(C)NC(=O)C=C(C)c1cccc(NC(=O)CCCC(=O)O)c1
Reaction #243594
DOI: 10.1039/C8SC04228D
CC(OC(=O)C(C)(C)C)C1CCC2C3CCC4NC(=O)C=CC4(C)C3CCC12C
Reaction #299816
DOI: 10.1039/C8SC04228D
CCCCCCCCCC(C)NC(=O)C=C(c1ccccc1)c1cccc(N)c1
Reaction #302815
DOI: 10.1039/C8SC04228D
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