Recherche de Sous-structure

CNCc1ccccc1

COc1ccc2[nH]cc(C(c3ccccc3)N(C)C)c2c1
Reaction #9080
[(5-Methoxy-1H-indol-3-yl)-phenylmethyl]-dimethylamine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CC(c3cccc(F)c3F)=CC[C@@H](NC(=O)OCc3ccccc3)C2=O)c(OC)c1
Reaction #42664
title compound
Rendement 57.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CC=C(c2cccc(F)c2F)CNC1=O)OCc1ccccc1
Reaction #42665
title compound
Rendement 66.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CC(c3cccc(F)c3F)=CC[C@@H](NC(=O)OCc3ccccc3)C2=O)c(OC)c1
Reaction #48408
title compound
Rendement 57.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CC=C(c2cccc(F)c2F)CNC1=O)OCc1ccccc1
Reaction #48409
title compound
Rendement 66.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C=C2c3ccccc3C(=O)NC2C)cn1
Reaction #77512
rac. 4-[1-(6-methoxy-pyridin-3-yl)-methylidene]-3-methyl-3,4-dihydro-2H-isoquinolin-1-one
DOI: 10.6084/m9.figshare.5104873.v1
C=C(CCl)CN(Cc1ccccc1)[C@@H](CC(=O)OC(C)(C)C)C(=O)OCc1ccccc1
Reaction #89694
(2S)-[benzyl-(2-chloromethyl-allyl)-amino]-succinic acid 1-benzyl ester 4-tert-butyl ester
Rendement 58.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(/C(=C/[C@H]2CCC(=O)N2)c2ccc(C(C)(C)C)cc2)ccc1Br
Reaction #157737
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(OC)c(=O)[nH]2)c(OC)c1
Reaction #157822
6-{(E)-1-(4-tert-butylphenyl)-2-[(2R)-1-(2,4-dimethoxybenzyl)-5-oxopyrrolidin-2-yl]ethenyl}-3-methoxypyridin-2(1H)-one
Rendement 39.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(/C(=C/[C@H]2CCC(=O)N2)c2ccc(C(C)(C)C)cc2)[nH]c1=O
Reaction #157823
title compound
Rendement 62.9%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(/C(=C/[C@H]2CCC(=O)N2Cc2ccc(OC)cc2OC)c2ccc(C(C)(C)C)cc2)[nH]c1=O
Reaction #157838
6-{(E)-1-(4-tert-butylphenyl)-2-[(2R)-1-(2,4-dimethoxybenzyl)-5-oxopyrrolidin-2-yl]ethenyl}-3-ethylpyridin-2(1H)-one
Rendement 85.3%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(/C(=C/[C@H]2CCC(=O)N2)c2ccc(C(C)(C)C)cc2)[nH]c1=O
Reaction #157839
title compound
Rendement 57.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(/C=C/CCO[Si](C)(C)C(C)(C)C)c(OC)n2)c(OC)c1
Reaction #157843
(5R)-5-[(E)-2-{5-[(1E)-4-{[tert-butyl(dimethyl)silyl]oxy}but-1-en-1-yl]-6-methoxypyridin-2-yl}-2-(4-tert-butylphenyl)ethenyl]-1-(2,4-dimethoxybenzyl)pyrrolidin-2-one
Rendement 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(C#N)c(OC)n2)c(OC)c1
Reaction #157854
6-{(E)-1-(4-tert-butylphenyl)-2-[(2R)-1-(2,4-dimethoxybenzyl)-5-oxopyrrolidin-2-yl]ethenyl}-2-methoxypyridine-3-carbonitrile
Rendement 40.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CCC2C=C(c2ccc(C(C)(C)C)cc2)c2ccc(C3(O)CCC3)c(OC)n2)c(OC)c1
Reaction #157856
5-{2-(4-tert-butylphenyl)-2-[5-(1-hydroxycyclobutyl)-6-methoxypyridin-2-yl]ethenyl}-1-(2,4-dimethoxybenzyl)pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(SC)c(OC)n2)c(OC)c1
Reaction #157859
(5R)-5-{(E)-2-(4-tert-butylphenyl)-2-[6-methoxy-5-(methylsulfanyl)pyridin-2-yl]ethenyl}-1-(2,4-dimethoxybenzyl)pyrrolidin-2-one
Rendement 34.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(Cl)cc2)c2ccc(-c3cn[nH]c3)c(OC)n2)c(OC)c1
Reaction #157872
(5R)-5-{(E)-2-(4-chlorophenyl)-2-[6-methoxy-5-(1H-pyrazol-4-yl)pyridin-2-yl]ethenyl}-1-(2,4-dimethoxybenzyl)pyrrolidin-2-one
Rendement 63.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O[C@H]1CN2CCC1CC2)C(Nc1cccc(OC(F)(F)F)c1)c1ccccc1
Reaction #164166
title compound
Rendement 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(COc1ccc(C(N)=O)cn1)NCc1ccccc1
Reaction #173125
DOI: 10.1039/C8SC04228D
COc1ccccc1CNC(=O)C(N)Cc1c[nH]c2ccccc12
Reaction #175371
DOI: 10.1039/C8SC04228D
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