21개 반응에 참여

169355

O=C(O)c1ccc(Cl)cc1Br
Reaction #7064
title compound
수율 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Nc1ncc(C(F)(F)F)cc1C#Cc1ccccc1
Reaction #42694
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCN(CCC)C(=O)c1cccc(C(=O)O)c1
Reaction #49221
title compound
수율 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(CBr)c1cccc2ccccc12
Reaction #54817
bromomethyl 1-naphthyl ketone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
Cc1ccc(Br)cc1I
Reaction #56873
5-bromo-2-methyl-1-iodo-benzene
수율 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1c(Br)cnc(C=O)c1[N+](=O)[O-]
Reaction #158180
5-bromo-4-methyl-3-nitropyridine-2-carboxaldehyde
수율 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(N)(C#N)Cn1cc2ncc(Br)cc2n1
Reaction #158186
2-Amino-3-(6-bromo-2H-pyrazolo[4,3-b]pyridin-2-yl)-2-methylpropionitrile
수율 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(Cc1ccccc1Cl)c1cc2c(s1)-c1ccc(Br)cc1OCC2
Reaction #171741
1-(8-Bromo-4,5-dihydrobenzo[b]thieno[2,3-d]oxepin-2-yl)-2-(2-chlorophenyl)ethanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)c1csc(CC)c1
Reaction #194956
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccc(Oc2ccc3c(c2)C(C)(C)CCC3(C)C)cc1
Reaction #196280
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(CC(=O)N1C(=O)OCC1c1ccccc1)c1ccc(Br)cc1
Reaction #198065
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(C)C(C)C(=O)N1C(=O)OCC1c1ccccc1
Reaction #206474
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1c(C)cc(C)c2c1OC(C)(C)C2=O
Reaction #222403
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccnc2c1cc(-c1ccncc1)n2-c1ccc(F)cc1
Reaction #242516
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1ccc(C#N)c(Br)c1
Reaction #244555
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(O)c1ccc(Cl)cc1Br
Reaction #249166
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Brc1ccc2c(c1)oc1ccccc12
Reaction #263460
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cccc(CC2CCCCC2(O)c2nc(-c3ccccc3)c(-c3ccccc3)o2)c1
Reaction #270813
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C=COC(=O)c1ccccc1
Reaction #279351
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C1c2c(ccc(Cl)c2Cl)CC1Br
Reaction #281886
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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