Recherche de Sous-structure

NCCc1ccccc1

COC(=O)[C@@H](Cc1ccccc1)N=Cc1ccccc1
Reaction #6020
N-benzylidene-D-phenylalanine methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H](O)Cc1ccccc1
Reaction #11018
(2S)-2-hydroxy-3-phenylpropionic acid
Rendement 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CNCCc1c(Cl)cccc1Cl
Reaction #46110
[2-(2,6-dichlorophenyl)ethyl]methylamine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(NCc2ccc(F)cc2)=N[C@@H](c2ccccc2)[C@H]1c1ccccc1
Reaction #47011
product 85
Rendement 41.6%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Fc1ccc(CNC2=N[C@@H](c3ccccc3)[C@@H](c3ccccc3)N2)cc1
Reaction #47012
product 86
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(NCc2cccc(F)c2)=N[C@@H](c2ccccc2)[C@H]1c1ccccc1
Reaction #47013
product 87
Rendement 62.1%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Fc1cccc(CNC2=N[C@@H](c3ccccc3)[C@@H](c3ccccc3)N2)c1
Reaction #47014
product 88
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(NCCc2ccccc2F)=N[C@@H](c2ccccc2)[C@H]1c1ccccc1
Reaction #47016
product 91
Rendement 43.2%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Fc1ccccc1CCNC1=N[C@@H](c2ccccc2)[C@@H](c2ccccc2)N1
Reaction #47017
product 92
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(NCCc2ccccc2)=N[C@@H](c2ccccc2)[C@H]1c1ccccc1
Reaction #47018
product 93
Rendement 44.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Oc1ccccc1)N1C(NCc2ccc(F)cc2)=N[C@@H](c2ccccc2)[C@H]1c1ccccc1
Reaction #47019
product 123
Rendement 82.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N=C(NC2CCCCCC2)SC1Cc1ccc(O)c(O)c1
Reaction #74336
2-(cycloheptylamino)-5-(3,4-dihydroxybenzyl)-1,3-thiazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(-c2ccc(Cl)cc2Cl)cn2ccnc12
Reaction #85941
6-(2,4-Dichlorophenyl)imidazo[1,2-a]pyrazin-8(7H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C[C@@H](Nc1nnnc2c(C(N)=O)cccc12)c1ccc(Cl)c(C#N)c1
Reaction #88253
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccnc(COc2ccc(C(C)=O)cc2-c2ccc3c(c2)CCN(C(=O)OC(C)(C)C)CC3)c1
Reaction #91558
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(OCc2cc(C)ccn2)c(-c2ccc3c(c2)CCNCC3)c1
Reaction #91563
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(OCc2ccccn2)c(-c2ccc3c(c2)CNCC3)c1
Reaction #91569
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1C(c2c(OC)cc(OC)cc2OC)CC(=O)N1C
Reaction #180024
DOI: 10.1039/C8SC04228D
CC(C)N1CCN(c2ccc(NC=C3C(=O)NC(=O)c4ccc(I)cc43)cc2)CC1
Reaction #195353
DOI: 10.1039/C8SC04228D
CNC(=O)Cc1ccc(Oc2ccnc3cc(C(=O)N4CCC(O)C4)sc23)cc1Cl
Reaction #198078
DOI: 10.1039/C8SC04228D
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