Substructure Search

10012

CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@@H](OC(=N)C(Cl)(Cl)Cl)SC[C@H]1OC(C)=O
Reaction #6127
expected product
Yield 53.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OC(=N)C(Cl)(Cl)Cl)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40596
21
Yield 37.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cnc2ccc(C(F)(F)c3nnc4c(F)cc(-c5cnn(C)c5)cn34)cc2c1
Reaction #68626
6-(difluoro(8-fluoro-6-(1-methyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[4,3-a]pyridin-3-yl)methyl)-3-methoxyquinoline
Yield 44.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2cc(F)c3nnc(C(F)(F)c4ccc5ncccc5c4)n3c2)cn1
Reaction #68659
6-(Difluoro(8-fluoro-6-(1-methyl-1H-pyrazol-4-yl)-[1,2,4]-triazolo[4,3-a]pyridin-3-yl)methyl)quinoline
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ccc(-c2nc3cccnc3o2)cc1
Reaction #68993
dimethyl-(4-oxazolo[5,4-b]pyridin-2-yl-phenyl)-amine
Yield 6.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(OC(=N)C(Cl)(Cl)Cl)c1ccccc1
Reaction #70827
2-phenylpropan-2-yl 2,2,2-trichloroacetimidate
Yield 103.7%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=N)C(Cl)(Cl)Cl
Reaction #81082
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)CCC(=O)O[C@H]1[C@H](OC(=N)C(Cl)(Cl)Cl)O[C@@H](C)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #90566
212
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@H]1O[C@@H](O[C@H]2[C@H](OC(=N)C(Cl)(Cl)Cl)O[C@@H](C)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)[C@H](NC(=O)C(Cl)(Cl)Cl)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #90568
306
Yield 79.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@H]1[C@H](O[C@H]2[C@H](OC(=N)C(Cl)(Cl)Cl)O[C@@H](C)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #90570
307
Yield 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](C)O[C@@H](O[C@@H]2[C@@H](O)[C@H](C)O[C@](O)([C@H]3O[C@H](COCc4ccccc4)[C@@H](OCc4ccccc4)[C@H](OCc4ccccc4)[C@H]3OCc3ccccc3)[C@@H]2OC(=O)c2ccccc2)[C@@H]1OC(C)=O.N=C(O)C(Cl)(Cl)Cl
Reaction #90573
505
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
N=C(OC1O[C@H](COC(=O)c2ccccc2)[C@@H](OC(=O)c2ccccc2)[C@H](OC(=O)c2ccccc2)[C@@H]1O[C@H]1O[C@H](COC(=O)c2ccccc2)[C@@H](OC(=O)c2ccccc2)[C@H](OC(=O)c2ccccc2)[C@@H]1OC(=O)c1ccccc1)C(Cl)(Cl)Cl
Reaction #162017
trichloroacetimidate
Yield 77.0%DOI: 10.6084/m9.figshare.5104873.v1
N=C(OC1O[C@H](COC(=O)c2ccccc2)[C@@H](OC(=O)c2ccccc2)[C@H](O[C@H]2O[C@H](COC(=O)c3ccccc3)[C@@H](OC(=O)c3ccccc3)[C@H](O[C@H]3O[C@H](COC(=O)c4ccccc4)[C@@H](OC(=O)c4ccccc4)[C@H](OC(=O)c4ccccc4)[C@@H]3OC(=O)c3ccccc3)[C@@H]2OC(=O)c2ccccc2)[C@@H]1OC(=O)c1ccccc1)C(Cl)(Cl)Cl
Reaction #162023
trichloroacetimidate
Yield 72.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(OC(=N)C(Cl)(Cl)Cl)c1cc(C(F)(F)F)cc(C(F)(F)F)c1
Reaction #178658
DOI: 10.1039/C8SC04228D
CC(=O)OC1C(COCc2ccccc2)OC(OC(=N)C(Cl)(Cl)Cl)C(OC(C)=O)C1OC(C)=O
Reaction #179800
DOI: 10.1039/C8SC04228D
COc1ccc(COC(=N)C(Cl)(Cl)Cl)cc1
Reaction #180015
DOI: 10.1039/C8SC04228D
N=C(OC(c1ccccc1)c1ccc(Br)cc1)C(Cl)(Cl)Cl
Reaction #181471
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CC(OC(=N)C(Cl)(Cl)Cl)CC1CC
Reaction #195817
DOI: 10.1039/C8SC04228D
N=C(OC(c1ccc(Br)cc1)C1CCCCC1)C(Cl)(Cl)Cl
Reaction #198600
DOI: 10.1039/C8SC04228D
N=C(OCc1ccc(F)cc1F)C(Cl)(Cl)Cl
Reaction #225444
DOI: 10.1039/C8SC04228D
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