Busqueda de Subestructura

3566

CCOC(=O)CCCOc1ccc(N2CCN(c3ccncc3)CC2)cc1
Reaction #2302
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCOc1ccc(N2CCN(c3ccncc3)CC2)cc1
Reaction #2305
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(O)CCCOc1ccc(N2CCN(c3ccncc3)CC2)cc1
Reaction #2337
title compound
Rendimiento 81.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(C)COc1ccc(N2CCN(c3ccncc3)CC2)cc1
Reaction #2339
ethyl 3-methyl-4-[4-[4-(4-pyridyl)piperazin-1-yl]phenoxy]butyrate
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(COc1ccc(N2CCN(c3ccncc3)CC2)cc1)CC(=O)OC
Reaction #2341
methyl 4-[4-[4-(4-pyridyl)piperazin-1-yl]-phenoxy]-3-vinylbutyrate
Rendimiento 19.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(N)CCOc1ccc(N2CCN(c3ccncc3)CC2)cc1
Reaction #2345
title compound
Rendimiento 74.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](COc1ccc(N2CCN(c3ccncc3)CC2)cc1)CC(=O)OC(C)(C)C
Reaction #2349
tert-butyl (3R)-3-methyl-4-[4-[4-(4-pyridyl)piperazin-1-yl]phenoxy]butyrate
Rendimiento 42.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC(COc1ccc(N2CCN(c3ccncc3)CC2)cc1)Cc1ccccc1
Reaction #232278
DOI: 10.1039/C8SC04228D
CCOC(=O)CCCOc1ccc(N2CCN(c3ccncc3)CC2)cc1
Reaction #353908
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCOc1ccc(N2CCN(c3ccncc3)CC2)cc1
Reaction #353911
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(O)CCCOc1ccc(N2CCN(c3ccncc3)CC2)cc1
Reaction #353943
title compound
Rendimiento 81.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(C)COc1ccc(N2CCN(c3ccncc3)CC2)cc1
Reaction #353945
ethyl 3-methyl-4-[4-[4-(4-pyridyl)piperazin-1-yl]phenoxy]butyrate
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(COc1ccc(N2CCN(c3ccncc3)CC2)cc1)CC(=O)OC
Reaction #353947
methyl 4-[4-[4-(4-pyridyl)piperazin-1-yl]-phenoxy]-3-vinylbutyrate
Rendimiento 19.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](COc1ccc(N2CCN(c3ccncc3)CC2)cc1)CC(=O)OC(C)(C)C
Reaction #353952
tert-butyl (3R)-3-methyl-4-[4-[4-(4-pyridyl)piperazin-1-yl]phenoxy]butyrate
Rendimiento 42.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCOc1ccc(N2CCN(c3ccncc3)CC2)cc1
Reaction #368715
DOI: 10.1039/C8SC04228D
CCOC(=O)CCCOc1ccc(N2CCN(c3ccncc3)CC2)cc1
Reaction #951975
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCOc1ccc(N2CCN(c3ccncc3)CC2)cc1
Reaction #951978
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(O)CCCOc1ccc(N2CCN(c3ccncc3)CC2)cc1
Reaction #952033
title compound
Rendimiento 81.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(C)COc1ccc(N2CCN(c3ccncc3)CC2)cc1
Reaction #952034
ethyl 3-methyl-4-[4-[4-(4-pyridyl)piperazin-1-yl]phenoxy]butyrate
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(COc1ccc(N2CCN(c3ccncc3)CC2)cc1)CC(=O)OC
Reaction #952036
methyl 4-[4-[4-(4-pyridyl)piperazin-1-yl]phenoxy]-3-vinylbutyrate
Rendimiento 19.6%DOI: 10.6084/m9.figshare.5104873.v1
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