Recherche de Sous-structure

385555

CC(=O)Nc1ccccc1OC(C)C1CO1
Reaction #260550
DOI: 10.1039/C8SC04228D
C=C1c2cccc(NC(=O)c3c(Cl)cccc3Cl)c2OC1(C)OC
Reaction #429647
7-(2,6-dichlorobenzoylamino)-2,3-dihydro-2-methoxy-2-methyl-3-methylenebenzo[b]furan
Rendement 25.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccccc1OC1C=CCC1
Reaction #583369
subtitle compound
Rendement 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccccc1OC1CCC2OC12
Reaction #583370
subtitle compound
Rendement 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccccc1OC1C=CCCC1
Reaction #583371
title compound
Rendement 19.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccccc1OC1CCCC2OC12
Reaction #583372
title compound
Rendement 73.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(C)Oc1ccccc1NC(C)=O
Reaction #583403
compound
Rendement 40.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccccc1OC(C)C1CO1
Reaction #583404
N-{2-[1-(2-Oxiranyl)ethoxy]phenyl}acetamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccccc1OC1C=CCC1
Reaction #671791
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccccc1OC1CCC2OC12
Reaction #671792
subtitle compound
Rendement 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccccc1OC1CCCC2OC12
Reaction #671793
title compound
Rendement 73.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(C)Oc1ccccc1NC(C)=O
Reaction #671823
compound
Rendement 40.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccccc1OC(C)C1CO1
Reaction #671824
N-{2-[1-(2-Oxiranyl)ethoxy]phenyl}acetamide
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(C)Oc1ccccc1NC(C)=O
Reaction #776191
DOI: 10.1039/C8SC04228D
CC(=O)Nc1ccccc1OC1CCC2OC12
Reaction #923291
DOI: 10.1039/C8SC04228D
CC(=O)Nc1ccccc1OC1C=CCC1
Reaction #1053071
subtitle compound
Rendement 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccccc1OC1CCC2OC12
Reaction #1053072
subtitle compound
Rendement 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccccc1OC1C=CCCC1
Reaction #1053073
title compound
Rendement 19.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccccc1OC1CCCC2OC12
Reaction #1053074
title compound
Rendement 73.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(C)Oc1ccccc1NC(C)=O
Reaction #1053105
compound
Rendement 40.2%DOI: 10.6084/m9.figshare.5104873.v1
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