Busqueda de Subestructura

O=Cc1cccc(Br)c1

CC(=O)c1cccc2c1NC(=O)C2
Reaction #4573
7-acetyloxindole
DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(CCCl)Oc2ccc(Br)cc2C1=O
Reaction #4898
brown solid
Rendimiento 60.2%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(CCCl)Oc2ccc(Br)cc2C1=S
Reaction #4904
yellow solid
Rendimiento 72.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(S(=O)(=O)Nc2ccc(Br)cc2C(=O)c2ccccc2)cc1
Reaction #47158
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C(F)(F)F)CC(=O)c2cc(Br)ccc2O1
Reaction #48332
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C(F)(F)F)C[C@@H](O)c2cc(Br)ccc2O1
Reaction #48333
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(NC(=O)OC(C)(C)C)cc(C)c1CNC(=O)c1cc(Br)cc2c1c(C)cn2C(C)C
Reaction #70707
tert-butyl (5-((6-bromo-1-isopropyl-3-methyl-1H-indole-4-carboxamido)methyl)-6-methoxy-4-methylpyridin-2-yl)carbamate
Rendimiento 99.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N)[nH]c(=O)c1CNC(=O)c1cc(Br)cc2c1c(C)cn2C(C)C
Reaction #70708
N-((6-amino-4-methyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-6-bromo-1-isopropyl-3-methyl-1H-indole-4-carboxamide
Rendimiento 28.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc2cc(Br)ccc2s1
Reaction #82231
2-acetyl-5-bromobenzo[b]thiophene
Rendimiento 40.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(NC(=O)OC(C)(C)C)cc(C)c1CNC(=O)c1cc(Br)cc2c1c(C)cn2C(C)C
Reaction #90606
tert-butyl (5-((6-bromo-1-isopropyl-3-methyl-1H-indole-4-carboxamido)methyl)-6-methoxy-4-methylpyridin-2-yl)carbamate
Rendimiento 99.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N)[nH]c(=O)c1CNC(=O)c1cc(Br)cc2c1c(C)cn2C(C)C
Reaction #90607
N-((6-amino-4-methyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-6-bromo-1-isopropyl-3-methyl-1H-indole-4-carboxamide
Rendimiento 28.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Br)cc(-c2ccc(C)cn2)c1
Reaction #164944
3-bromo-5-(5-methyl-pyridin-2-yl)-benzoic acid methyl ester
Rendimiento 51.2%DOI: 10.6084/m9.figshare.5104873.v1
COCCn1c(C)c(C)s/c1=N\C(=O)c1cc(Br)cc2c1OCC2
Reaction #165618
title compound
Rendimiento 36.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2cc(Br)ccc2OCCC1Br
Reaction #171816
4,7-dibromo-3,4-dihydro-2H-benzo[b]oxepin-5-one
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(O)CN(Cc1ccc(S(C)(=O)=O)cc1)C(=O)c1ccc(Br)cc1C(=O)c1ccccc1
Reaction #177045
DOI: 10.1039/C8SC04228D
COC(=O)C1CCSc2ccc(Br)cc2C1=O
Reaction #177734
DOI: 10.1039/C8SC04228D
C=C1CC(c2ccccc2)Oc2ccc(Br)cc21
Reaction #179782
DOI: 10.1039/C8SC04228D
COC(=O)C1=Cc2cc(Br)ccc2SCC1
Reaction #187471
DOI: 10.1039/C8SC04228D
CCOP(=O)(Cc1ccc(Nc2ncc(C(F)(F)F)c(Nc3ccc(-c4ccc(C(=O)O)cc4)c4c3C(=O)N(C)C4)n2)c(OC)c1)OCC
Reaction #189132
DOI: 10.1039/C8SC04228D
CCCCCC(=O)c1cc(Br)cc2c1OCC2(C)C
Reaction #189883
DOI: 10.1039/C8SC04228D
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