Busqueda de Subestructura

1345319

Cc1oc(-c2ccccc2)nc1COc1ccc2cc(CC3OC(=O)NC3=O)oc2c1
Reaction #1146
5-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranylmethyl]-2,4-oxazolidinedione
Rendimiento 6.6%DOI: 10.6084/m9.figshare.5104873.v1
CC1(I)OC(=O)N(c2ccc(Cl)cc2)C1=O
Reaction #54745
3-(4-Chlorophenyl)-5-iodo-5-methyl-oxazolidine-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
Cn1ncc(/C=C/C(=O)Nc2ccc(CC3OC(=O)NC3=O)cc2)c1-c1ccc(F)cc1
Reaction #58990
(2E)-N-{4-[(2,4-dioxo-1,3-oxazolidin-5-yl)methyl]phenyl}-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]acrylamide
Rendimiento 77.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)C(c2ccc(C(=O)c3ccccc3)s2)O1
Reaction #177011
DOI: 10.1039/C8SC04228D
Cl
Reaction #179453
DOI: 10.1039/C8SC04228D
CC1(I)OC(=O)N(c2ccc(Cl)cc2)C1=O
Reaction #181220
DOI: 10.1039/C8SC04228D
Cc1oc(-c2ccccc2)nc1CCOc1ccc(C=CC=CC=C2OC(=O)NC2=O)cc1
Reaction #182661
DOI: 10.1039/C8SC04228D
O=C1COC(=O)N1CCc1ccc(-c2ccc(Cl)cc2)cc1
Reaction #187109
DOI: 10.1039/C8SC04228D
CN(C(=O)N(C)C1CCN(C(=O)CN2C(=O)OC(C)(C)C2=O)CC1c1ccc(F)cc1)c1cc(C(F)(F)F)cc(C(F)(F)F)c1
Reaction #191292
DOI: 10.1039/C8SC04228D
C=CN1C(=O)OC(C)C1=O
Reaction #194087
DOI: 10.1039/C8SC04228D
COc1ccc(Cl)cc1C1OC(=O)N(C(C)=O)C1=O
Reaction #195633
DOI: 10.1039/C8SC04228D
CCOc1ccccc1C1OC(=O)NC1=O
Reaction #198978
DOI: 10.1039/C8SC04228D
COc1cc(CCCC2OC(=O)NC2=O)ccc1OCc1coc(CCc2ccccc2)n1
Reaction #200093
DOI: 10.1039/C8SC04228D
CC1(C)OC(=O)N(CCc2ccccc2Br)C1=O
Reaction #206857
DOI: 10.1039/C8SC04228D
CN(C(=O)N(C)C1CN(C(=O)CN2C(=O)OC(C)(C)C2=O)CC1c1ccc(F)cc1)c1cc(C(F)(F)F)cc(C(F)(F)F)c1
Reaction #210725
DOI: 10.1039/C8SC04228D
COc1ccc(Cl)cc1C1OC(=O)N(C(C)=O)C1=O
Reaction #228707
DOI: 10.1039/C8SC04228D
CC(C)C1OC(=O)N(c2cc(O)c(Cl)cc2F)C1=O
Reaction #230301
DOI: 10.1039/C8SC04228D
O=C1COC(=O)N1CC1CCN(c2nccc3ccccc23)CC1
Reaction #232450
DOI: 10.1039/C8SC04228D
Cc1oc(-c2ccccc2)nc1CCOc1ccc(CCCCC2OC(=O)NC2=O)cc1
Reaction #251767
DOI: 10.1039/C8SC04228D
CC1(C(F)(F)F)OC(=O)N(c2ccc(Cl)c(Cl)c2)C1=O
Reaction #262033
DOI: 10.1039/C8SC04228D
Página 1Siguiente