Substructure Search

226199

CCOC(=O)c1ccc(/C=C/c2cccc3c2C(Sc2ccccc2)=CCC3(C)C)cc1
Reaction #1466
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC[C@H](NC(=O)c1ccc(C(=Cn2cnc3nc(NC(=O)C(C)(C)C)cc-3c2O)COC2CCCCO2)cc1)C(=O)OCC
Reaction #6625
diethyl N-[4-{1-(tetrahydropyr-2-yloxy)-3-(4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidin-3-yl)prop-2-en-2yl}benzoyl]glutamate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC[C@H](NC(=O)c1ccc(C(COC2CCCCO2)Cn2cnc3nc(NC(=O)C(C)(C)C)cc-3c2O)cc1)C(=O)OCC
Reaction #6628
diethyl N-[4-{1-(tetrahydropyr-2-yloxy)-3-(4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidin-3-yl)prop--2-yl}benzoyl]glutamate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC2Cc3ccc(C(=CC(=O)O)c4cccnc4)cc3C2)cc1
Reaction #50404
3-(2-(4-Toluenesulphonylamino)indan-5-yl)-3-(3-pyridyl)-prop-2-enoic acid
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc(-c2c[nH]nc2C(F)(F)F)cc1SCC(F)(F)F
Reaction #53575
[2-ethenyl-5-(3-trifluoromethylpyrazolyl)phenyl] 2,2,2-trifluoroethyl sulfide
Yield 43.8%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)c1cc(C)c(C)cc1C1=CCN(C(=O)OC(C)(C)C)CC1
Reaction #58002
84
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)c1cc(C)c(C)cc1C1CCN(C(=O)OC(C)(C)C)CC1
Reaction #58003
85
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](O)c1cc(C)c(C)cc1C1=CCN(C(=O)OC(C)(C)C)CC1
Reaction #58005
azide
DOI: 10.6084/m9.figshare.5104873.v1
N=C(C=Cc1ccc(-c2ccc3[nH]ccc3c2)cc1)Nc1ccc(Cl)cc1
Reaction #58713
N-(4-chloro-phenyl)-3-[4-(1H -indol-5-yl)-phenyl]-acrylamidine
Yield 44.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc2cc(-c3ccc(C=CC(=N)Nc4ccc(Cl)cc4)cc3)ccc21
Reaction #58714
N-(4-chloro-phenyl)-3-[4-(1-methyl-1H-indol-5-yl)-phenyl]-acrylamidine
Yield 26.9%DOI: 10.6084/m9.figshare.5104873.v1
CON=C(C)c1ccc(-c2ccc(C=CC(=N)Nc3ccc(Cl)cc3)cc2)cc1
Reaction #58717
N-(4-chloro-phenyl)-3-[4′-(1-methoxyimino-ethyl)-biphenyl-4-yl]-acrylamidine
Yield 9.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)c1ccc(C(=O)OC)c(Cl)c1
Reaction #88839
2-chloro-4-isopropenyl-benzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C(C)C)cc1Cl
Reaction #88840
2-chloro-4-isopropyl-benzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CNCCOC(=O)C(C)(C)C)ccc1C=Cc1cccs1
Reaction #172492
2,2-dimethylpropionic acid 2-{[3-methoxy-4-(2-thiophene-2-ylvinyl)phenyl]methylamino}ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CNCCO)ccc1C=Cc1cccs1
Reaction #172493
2-{[3-methoxy-4-(2-thiophene-2-ylvinyl)phenyl]methylamino}ethanol
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(C(=O)O)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)OC)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172733
title compound
Yield 99.1%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(N=C=O)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)OC)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172734
title compound
Yield 86.4%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NCC3(NC(=O)OC(C)(C)C)CC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)OC)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172735
title compound
Yield 66.5%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NC(=O)NCC(C)(C)N3CCOCC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172739
title compound
Yield 20.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NC(=O)C(=O)N(C)C)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172754
title compound
Yield 13.0%DOI: 10.6084/m9.figshare.5104873.v1
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