Recherche de Sous-structure

C1COCCC1CI

CCOC(=O)C(CC1CCOCC1)c1ccc2c(c1)N(C)c1ccccc1S2(=O)=O
Reaction #43265
Ethyl 2-(10-methyl-5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-3-(tetrahydropyran-4-yl)propionate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCC1(F)CCN(CC2(C(=O)OCc3ccccc3)CCOCC2)CC1
Reaction #44888
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)c2c(Nc3ccccc3)nn(CC3CCOCC3)c2N2C1=N[C@@H]1CCC[C@@H]12
Reaction #159876
(6aR,9aS)-5,6a,7,8,9,9a-hexahydro-5-methyl-3-(phenylamino)-1-((tetrahydro-2H-pyran-4-yl)methyl)-cyclopent[4,5]imidazo[1,2-a]pyrazolo[4,3-e]pyrimidin-4(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1C(=O)/N=c1\sc(C(C)(C)C)cn1CC1CCOCC1
Reaction #165681
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CC1CCOCC1)c1ccc(S(C)(=O)=O)cc1
Reaction #187804
DOI: 10.1039/C8SC04228D
COC(=O)C1(CSC(C)=O)CCOCC1
Reaction #198359
DOI: 10.1039/C8SC04228D
CON(C)C(=O)C(CC1CCOCC1)c1ccc(C(=O)OC(C)(C)C)cc1
Reaction #287355
DOI: 10.1039/C8SC04228D
COC(=O)C1(CSC(C)=O)CCOCC1
Reaction #292108
DOI: 10.1039/C8SC04228D
COC(=O)C1(CI)CCCCC1
Reaction #296018
DOI: 10.1039/C8SC04228D
[N-]=[N+]=NCC1CCOCC1
Reaction #327941
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1C(=O)/N=c1\sc(C(C)(C)C)cn1CC1CCOCC1
Reaction #341832
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(CI)CCOCC1
Reaction #406819
DOI: 10.1039/C8SC04228D
COC(=O)C1(CI)CCOCC1
Reaction #480871
title compound
Rendement 53.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(CSC(C)=O)CCOCC1
Reaction #480872
title compound
Rendement 97.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(CI)CCCCC1
Reaction #480917
title compound
Rendement 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1C(=O)/N=c1\sc(C(C)(C)C)cn1CC1CCOCC1
Reaction #625973
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(C2(CI)CCOCC2)cn1
Reaction #683111
2-fluoro-5-(4-(iodomethyl)tetrahydro-2H-pyran-4-yl)pyridine
Rendement 60.6%DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2ccc(F)nc2)CCOCC1
Reaction #683112
2-fluoro-5-(4-methyltetrahydro-2H-pyran-4-yl)pyridine
Rendement 54.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCC1(F)CCN(CC2(C(=O)OCc3ccccc3)CCOCC2)CC1
Reaction #733178
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(F)(F)F)nn1C(CC1CCOCC1)C(=O)N1CCCc2c1cnn2-c1ccc(F)cc1
Reaction #797848
desired product
Rendement 6.0%DOI: 10.6084/m9.figshare.5104873.v1
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