4-Bromomethylbenzophenone

O=C(c1ccccc1)c1ccc(CO)cc1
Reaction #68727
3
收率 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
NN=C(c1ccccc1)c1ccc(CO)cc1
Reaction #68728
4
收率 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C=CCOCc1ccc(C(=O)c2ccccc2)cc1
Reaction #68730
9
收率 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCN(CCOCc1ccc(C(=O)c2ccccc2)cc1)c1ccccc1
Reaction #75451
desired product
收率 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCOC(=O)C=Cc1ccc(N(C(=O)OC(C)(C)C)C2CCN(Cc3ccc(C(=O)c4ccccc4)cc3)C2)nc1
Reaction #180912
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(c1ccccc1)c1ccc(CO)cc1
Reaction #208705
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOP(=O)(Cc1ccc(C(=O)c2ccccc2)cc1)OCC
Reaction #250144
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)C(=O)Nc1cccc(C2CCN(Cc3ccc(C(=O)c4ccccc4)cc3)CC2)c1
Reaction #273689
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(c1ccccc1)c1ccc(CN2Cc3ccccc3C2=O)cc1
Reaction #276510
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CNCc1ccc(C(=O)c2ccccc2)cc1
Reaction #290595
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)/C=C/c1ccc(N(C(=O)OC(C)(C)C)[C@@H]2CCN(Cc3ccc(C(=O)c4ccccc4)cc3)C2)nc1
Reaction #313509
ethyl (2E)-3-{6-[[(3R)-1-(4-benzoylbenzyl)-3-pyrrolidinyl](tert-butoxycarbonyl)amino]-3-pyridyl}acrylate
收率 77.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CCN(CCOCc1ccc(C(=O)c2ccccc2)cc1)c1ccccc1
Reaction #390488
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CNCc1ccc(C(=O)c2ccccc2)cc1
Reaction #523014
4-benzoyl N-methyl benzyl amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_02
CCN(CCOCc1ccc(C(=O)c2ccccc2)cc1)c1ccccc1
Reaction #635023
desired product ( XIV )
收率 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
BrCc1ccc(Cc2ccccc2)cc1
Reaction #751313
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCc1nc2c(C)cc(C)nc2n1Cc1ccc(C(=O)c2ccccc2)cc1
Reaction #762366
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
C=CC(=O)OCC[N+](C)(C)Cc1ccc(C(=O)c2ccccc2)cc1
Reaction #913008
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
Cl.O=C(c1ccccc1)c1ccc(CSc2c(Cl)ccc3c2CCNCC3)cc1
Reaction #998692
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_09
CCOC(=O)C(Cc1ccc(C(=O)c2ccccc2)cc1)C(=O)OCC
Reaction #1018873
1,3-diethyl 2-[(4-benzoylphenyl)methyl]propanedioate
收率 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
C=CCOCc1ccc(C(=O)c2ccccc2)cc1
Reaction #1032917
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
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