Busqueda de Subestructura

CCOC(=O)c1cncc(Br)c1

CCOC(=O)c1cncc(N2CCOCC2)c1
Reaction #334
Rendimiento 0.0%
CCOC(=O)c1cncc(N2CCOCC2)c1
Reaction #335
Rendimiento 0.0%
CC(C)(C)OC(=O)c1cncc(N2CCOCC2)c1
Reaction #336
Rendimiento 26.6%
CCOC(=O)c1cncc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)c1
Reaction #72033
title compound
Rendimiento 51.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(Br)c2ccccn2c1=O
Reaction #77185
ethyl 1-bromo-4-oxo-4H-quinolizine-3-carboxylate
Rendimiento 71.0%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@]1(C(=O)O)CN(c2cncc(C(=O)O)c2)C[C@@H]1CCCB(O)O
Reaction #89649
5-((3R,4S)-3-amino-4-(3-boronopropyl)-3-carboxypyrrolidin-1-yl)nicotinic acid
Rendimiento 48.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(Br)c(OCc2c(-c3ccccc3)noc2C)nc1C
Reaction #170356
title compound
Rendimiento 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cncc(-c2cnn3cc(-c4ccc(OC)cc4)cnc23)c1
Reaction #188450
DOI: 10.1039/C8SC04228D
Cc1c(Br)c(=O)c(C=O)c(C)n1Cc1c(F)cccc1F
Reaction #192900
DOI: 10.1039/C8SC04228D
Cc1nc(OCC2CC2)c(Br)cc1C(=O)O
Reaction #194518
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc(Br)c(=O)[nH]c1C(F)(F)F
Reaction #249337
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc(Br)c(OCC2CC2)nc1C(F)(F)F
Reaction #253168
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc(Br)c(OCC2CC2)nc1C
Reaction #282959
DOI: 10.1039/C8SC04228D
O=C1Nc2ccccc2C1=C1OC(c2ccccc2)c2c(Br)cncc21
Reaction #283361
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc(-c2ccc(Cl)cc2)c(OCC2CC2)nc1C(F)(F)F
Reaction #295540
DOI: 10.1039/C8SC04228D
O=C(OCCO)c1cnc(Cl)c(Br)c1
Reaction #299587
DOI: 10.1039/C8SC04228D
O=C(O)c1cc(Br)c(=O)[nH]c1C(F)(F)F
Reaction #300973
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cncc(N2C[C@H]3CN(C(=O)OC(C)(C)C)C[C@H]3C2)c1
Reaction #327685
title compound
Rendimiento 94.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #328609
solid
Rendimiento 93.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(C#N)cnc1C(F)F
Reaction #328610
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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