Busqueda de Subestructura

1382319

COC(=O)c1cc2ccc(Cl)cc2nc1C(=O)OC
Reaction #3212
solid
Rendimiento 134.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(Cl)cc(C(=O)O)nc2c1
Reaction #6780
2-carboxy-7-methyl-4-chloroquinoline
Rendimiento 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)c1cc(Oc2ccc(N)c([N+](=O)[O-])c2)ccn1
Reaction #41724
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cnc(C(=O)O)cc1Cl
Reaction #63219
4-chloro-5-methoxy-2-pyridinecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CN(S(=O)(=O)c2ccc(C(F)(F)F)cc2)CCN1C(=O)c1cc(Cl)ccn1
Reaction #69596
title compound
Rendimiento 39.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)ccn1
Reaction #72030
title compound
Rendimiento 32.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)cc(C)n1
Reaction #72044
title compound
Rendimiento 34.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Cl)c(Cl)c(Cl)n1
Reaction #87871
title compound
Rendimiento 35.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Cl)c(Cl)c(Cl)n1
Reaction #87872
title compound
Rendimiento 33.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Cl)c(Cl)c(Cl)n1
Reaction #87873
title compound
Rendimiento 35.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Cl)c(Cl)c(Cl)n1
Reaction #87874
title compound
Rendimiento 83.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Cl)c(Cl)c(Cl)n1
Reaction #87875
4,5,6-trichloropicolinic Acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Cl)c(Cl)c(Cl)n1
Reaction #87876
4,5,6-trichloropicolinic Acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Cl)c(Cl)c(Cl)n1
Reaction #87877
4,5,6-trichloropicolinic Acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Cl)c(Cl)c(Cl)n1
Reaction #87878
4,5,6-trichloropicolinic Acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Cl)c(Cl)c(Cl)n1
Reaction #87879
4,5,6-trichloropicolinic Acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Cl)c(Cl)c(Cl)n1
Reaction #87880
title compound
Rendimiento 133.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc(Cl)ccn1)N1CCc2cc(F)ccc21
Reaction #161691
(4-chloropyridin-2-yl)-(5-fluoro-2,3-dihydroindol-1-yl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc(Cl)ccn1)N1CCc2c1ccc(F)c2F
Reaction #161730
(4-chloro-pyridin-2-yl)-(4,5-difluoro-2,3-dihydro-indol-1-yl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CN(C(=O)c2cc(Cl)ccn2)c2ccc(F)cc21
Reaction #161764
(4-chloro-pyridin-2-yl)-(5-fluoro-3,3-dimethyl-2,3-dihydro-indol-1-yl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1
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