Substructure Search

1198048

N#Cc1ccc(C(=O)C23CCCN2C(=O)N(c2cc(Cl)cc(Cl)c2)C3=O)cc1
Reaction #248634
DOI: 10.1039/C8SC04228D
CC(=O)NC1CN2C(=O)N(c3cc(Cl)cc(Cl)c3)C(=O)C2(Cc2ccc(C#N)cc2)C1
Reaction #255004
DOI: 10.1039/C8SC04228D
N#Cc1ccc(C(O)C23CCCN2C(=O)N(c2cc(Cl)cc(Cl)c2)C3=O)cc1
Reaction #297550
DOI: 10.1039/C8SC04228D
N#Cc1ccc(CC23CCCN2C(=O)N(c2cc(Cl)c(N)c(Cl)c2)C3=O)cc1
Reaction #381380
DOI: 10.1039/C8SC04228D
N#Cc1ccc(CC23CC(NC(=O)CCC(N)=O)CN2C(=O)N(c2cc(Cl)cc(Cl)c2)C3=O)cc1
Reaction #1227221
DOI: 10.1039/C8SC04228D
O=C1N(c2cc(Cl)cc(Cl)c2)C(=O)C2(Cc3ccc(-c4nnn[nH]4)cc3)CCCN12
Reaction #1479372
titled compound
Yield 17.8%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(CC23CCCN2C(=O)N(c2cc(Cl)c(N)c(Cl)c2)C3=O)cc1
Reaction #1479373
titled compound
Yield 68.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CC23CCCN2C(=O)N(c2cc(Cl)c(O)c(Cl)c2)C3=O)cc1
Reaction #1479375
5-(4-Methoxycarbonylbenzyl)-3-(3,5-dichloro-4-hydroxyphenyl)-1,3-diazabicyclo[3.3.0]octane-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C(O)C23CCCN2C(=O)N(c2cc(Cl)cc(Cl)c2)C3=O)cc1
Reaction #2269804
titled product
Yield 66.9%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C(=O)C23CCCN2C(=O)N(c2cc(Cl)cc(Cl)c2)C3=O)cc1
Reaction #2269805
titled compound
Yield 50.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(c2cc(Cl)cc(Cl)c2)C(=O)C2(Cc3ccc(-c4nnn[nH]4)cc3)CCCN12
Reaction #2269806
titled compound
Yield 17.8%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(CC23CCCN2C(=O)N(c2cc(Cl)c(N)c(Cl)c2)C3=O)cc1
Reaction #2269807
titled compound
Yield 68.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CC23CCCN2C(=O)N(c2cc(Cl)c(O)c(Cl)c2)C3=O)cc1
Reaction #2269810
5-(4-Methoxycarbonylbenzyl)-3-(3,5-dichloro-4-hydroxyphenyl)-1,3-diazabicyclo[3.3.0]octane-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H]1CN2C(=O)N(c3cc(Cl)cc(Cl)c3)C(=O)[C@]2(Cc2ccc(C#N)cc2)C1
Reaction #2310512
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C[C@@]23C[C@H](NC(=O)CCC(N)=O)CN2C(=O)N(c2cc(Cl)cc(Cl)c2)C3=O)cc1
Reaction #2310513
titled compound
Yield 70.3%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C[C@@]23C[C@H](NC(=O)CC(N)=O)CN2C(=O)N(c2cc(Cl)cc(Cl)c2)C3=O)cc1
Reaction #2310514
titled compound
Yield 88.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(CC23CC(NC(=O)CC(N)=O)CN2C(=O)N(c2cc(Cl)cc(Cl)c2)C3=O)cc1
Reaction #2436219
DOI: 10.1039/C8SC04228D