Substructure Search

40472

O=C(NCC1CC(=O)N(Cc2ccccc2)C1)Nc1ccc(Cl)cc1
Reaction #62799
title compound
Yield 74.9%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #75284
12.4
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2CCCCC2C(=O)N1c1ccc(Br)cc1F
Reaction #75286
2-(4-bromo-2-fluorophenyl)-3a,4,5,6,7,7a-hexahydro-1H-isoindole-1,3(2H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N2C(=O)C3CCCCC3C2=O)c(F)c1
Reaction #75288
4-(1,3-dioxo-2,3,3a,4,5,6,7,7a-octahydro-1H-isoindol-2-yl)-3-fluorobenzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1C2C(=O)N(Cc3ccccc3)C(=O)C12
Reaction #82989
ethyl 3-benzyl-2,4-dioxo-3-azabicyclo[3.1.0]hexane-6-carboxylate
Yield 726.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1CCC(=O)N1Cc1ccc(C#N)cc1
Reaction #83394
N-(4-Cyanobenzyl)-L-pyroglutamic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(CN2C(=O)CC[C@H]2C(=O)O)cc1
Reaction #83395
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N2CCC(C(=O)O)C2=O)cc1C
Reaction #86875
1-(3,4-dimethylphenyl)-2-oxopyrrolidine-3-carboxylic acid
Yield 86.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCc1c[nH]c2ccc(Cl)cc12)C1CCN(c2ccc3c(c2)COC3)C1=O
Reaction #87004
N-(2-(5-chloro-1H-indol-3-yl)ethyl)-1-(1,3-dihydroisobenzofuran-5-yl)-2-oxopyrrolidine-3-carboxamide
Yield 36.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N2CCC(C(=O)NCCc3c[nH]c4ccc(Cl)cc34)C2=O)cc1C
Reaction #87007
N-(2-(5-chloro-1H-indol-3-yl)ethyl)-1-(3,4-dimethylphenyl)-2-oxopyrrolidine-3-carboxamide
Yield 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CC#CCC(C)C(O)/C=C/[C@H]1CC(F)(F)C(=O)N1CCCCCCC(=O)OC
Reaction #87986
title compound
Yield 87.6%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #93639
B7
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCNC(=O)C=Cc1cccc(N2CC(C(=O)OCCN(CC)CC)CC2=O)c1
Reaction #95076
N-Decyl-3-(3-[4-(2-[N,N-diethylamino]ethoxycarbonyl)-2-oxo-pyrrolidino]phenyl)propenamide
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #95079
material
Yield 21.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #170665
crude product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C[C@@H](C(=O)N3C(=O)OC[C@H]3Cc3ccccc3)[C@H](C)C2=O)c(OC)c1
Reaction #170666
titled compound
Yield 54.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C[C@@H](C(=O)O)[C@H](C)C2=O)c(OC)c1
Reaction #170667
titled compound
Yield 109.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1C(=O)NC[C@@H]1C(=O)O
Reaction #170668
titled compound
Yield 56.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1CC(Cc2ccc(-c3ccccc3)cc2)N(C(=O)C(C)(C)C)C1=O
Reaction #176907
DOI: 10.1039/C8SC04228D
COC(=O)C1CC(=O)N(C(C)c2ccccc2)C1
Reaction #181390
DOI: 10.1039/C8SC04228D
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