Participa en 36 reacciones

175698

O=C1C2CCCC2Nc2ccccc2N1Cc1ccccc1
Reaction #181397
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1Nc2ccccc2NC2CCCC12
Reaction #225717
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)C(C#N)Cc1cc(OC)c(OC)c2c1C=CCO2
Reaction #247616
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)c1nc2c(c(-c3ccc(F)cc3)n1)CCC(N1CCCC1)C2
Reaction #260213
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cl
Reaction #267001
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)C(Cc1cnc(N)s1)C(=O)OCC
Reaction #267697
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CSCCCOc1cccc(Br)c1C
Reaction #324681
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CCOC(=O)C1C(c2ccc3c(c2)OCO3)CNC1c1ccc(OC)cc1
Reaction #373520
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cl
Reaction #384364
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1c(Br)cccc1OC12CC3CC(CC(C3)C1)C2
Reaction #423771
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
Cc1c(Br)cccc1OC12CC3CC(CC(C3)C1)C2
Reaction #675848
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
Cc1c(O)cccc1C#N
Reaction #716550
title compound
Rendimiento 49.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
NC(Cc1nccs1)c1ccc(Cl)cc1
Reaction #915318
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
COC(=O)C12CCC(C(=O)Cl)(CC1)CC2
Reaction #920597
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CC(C)(C)OC(=O)NCC1(CC(=O)O)CCCCC1
Reaction #1022073
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
COc1ccc(C(=O)c2ccc3ccccc3c2)c(Br)c1
Reaction #1153548
title compound
Rendimiento 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_06
Cc1c(C)c2c(c(C)c1NC(=O)OC(C)(C)C)CC(C)(CN1CCC(CCNC(c3ccccc3)c3ccccc3)CC1)O2
Reaction #1308400
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CCOC(=O)/C=C/c1cccc(O)c1C
Reaction #1337288
trans-3-(3-hydroxy-2-methylphenyl)acrylic acid ethyl ester
Rendimiento 43.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_01
Cc1c(Br)cccc1OCC(=O)OC(C)(C)C
Reaction #1337289
(3-bromo-2-methylphenoxy)acetic acid tert-butyl ester
Rendimiento 101.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_01
Cc1c(Br)cccc1OCC1CCCCC1
Reaction #1517434
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_01
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