Recherche de Sous-structure

CCOCC.Cl

C[C@@H](C(=O)N1CCOCC1)N1CC[C@H](NS(=O)(=O)/C=C/c2ccc(Cl)c(O)c2)C1=O
Reaction #7419
title compound
Rendement 83.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ncn(-c2cc(F)ccc2CNC(=O)c2nc3n(c(=O)c2O)CCOC3(CO)CCl)n1
Reaction #56658
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(c2ccc3c(=O)c(C(=O)O)cn(C4CC4)c3c2OC)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #72011
title compound
Rendement 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[Si](OCc1cc(C2(O)O[C@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)ccc1Cl)(C(C)C)C(C)C
Reaction #74464
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[Si](OCc1cc(C2O[C@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)ccc1Cl)(C(C)C)C(C)C
Reaction #74465
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCCOC1(c2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCN(C(=O)c3ccccc3)C2)CC1.Cl
Reaction #78350
expected product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cn(C(C[C@H]2CCCCO2)C(=O)O)c(=O)cc1-c1cc(Cl)ccc1OC(F)F
Reaction #85205
2-{4-[5-Chloro-2-(difluoromethoxy)phenyl]-5-methoxy-2-oxopyridin-1(2H)-yl}-3-[(2R)-tetrahydro-2H-pyran-2-yl]propanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1cn(C(C[C@H]2CCCCO2)C(=O)Nc2ccc(C(=O)OC(C)(C)C)cc2)c(=O)cc1-c1cc(Cl)ccc1OC(F)F
Reaction #85206
tert-Butyl 4-[(2-{4-[5-chloro-2-(difluoromethoxy)phenyl]-5-methoxy-2-oxopyridin-1(2H)-yl}-3-[(2R)-tetrahydro-2H-pyran-2-yl]propanoyl)amino]benzoate
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
Rendement 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=C(C(=O)OCC(Cl)(Cl)Cl)N1C(=O)C2N=C(COc3ccccc3)SC21)N1CCOCC1
Reaction #96108
2,2,2-trichloroethyl α-[3-phenoxymethyl-7-oxo-4-thia-2,6-diazabicyclo[3,2,0]hept-2-en-6-yl]-α-(1-morpholinoethylidene)acetate
Rendement 50.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC[C@H]1O[C@H](O[C@@H]2[C@H](OC(=O)c3ccccc3)[C@@H](O[C@@H]3[C@H](OC(=O)c4ccccc4)[C@@H](OCc4ccccc4)O[C@H](COC(=O)c4ccccc4)[C@H]3OC(=O)c3ccccc3)O[C@H](COC(=O)c3ccccc3)[C@H]2OC(=O)c2ccccc2)[C@@H](OC(=O)c2ccccc2)[C@@H](OC(=O)c2ccccc2)[C@@H]1OC(=O)c1ccccc1)c1ccccc1
Reaction #162021
trisaccharide
Rendement 60.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(CC=Cc1ccc(C2(O)CCOCC2)cc1)C(=O)O)c1c(Cl)cccc1Cl
Reaction #175872
DOI: 10.1039/C8SC04228D
C#Cc1ccc(Cc2cc(C3(O)OC(CO)C(O)C(O)C3O)ccc2Cl)cc1
Reaction #181164
DOI: 10.1039/C8SC04228D
COC1(c2ccc(Cl)c(Cc3ccc(OCCOC4CC4)cc3)c2)OC(C=O)C(OCc2ccccc2)C(OCc2ccccc2)C1OCc1ccccc1
Reaction #189706
DOI: 10.1039/C8SC04228D
COC1(c2ccc(Cl)c(Cc3ccc(OC(F)(F)F)cc3)c2)OC(CO)C(OCc2ccccc2)C(OCc2ccccc2)C1OCc1ccccc1
Reaction #191865
DOI: 10.1039/C8SC04228D
CCOc1ccc(Cc2cc(C3(OC)OC(CO)(CO)C(OCc4ccccc4)C(OCc4ccccc4)C3OCc3ccccc3)ccc2Cl)c(F)c1F
Reaction #198218
DOI: 10.1039/C8SC04228D
CCCCC(Oc1ccc(C=CC(=O)OCC)c(Cl)c1)c1cccc(-c2ccc(C(F)(F)F)cc2)n1
Reaction #210041
DOI: 10.1039/C8SC04228D
OCC1OC(O)(c2ccc(Cl)c(Cc3ccc(OC4CCCC4O)cc3)c2)C(O)C(O)C1O
Reaction #210930
DOI: 10.1039/C8SC04228D
CCOC(=O)c1ccc(COc2ccc(C(C)C(O)(c3ccnc(C)c3)C(F)(F)F)c(Cl)c2)cn1
Reaction #212796
DOI: 10.1039/C8SC04228D
CC(Nc1c(F)ccc(Cl)c1F)c1cc(C(=O)N(C)C)cc2c(=O)cc(N3CCOCC3)oc12
Reaction #231409
DOI: 10.1039/C8SC04228D
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