phenylacetaldehyde

c1ccc(CC2SCCCS2)cc1
Reaction #6482
title compound
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)(C)OC(=O)N1CCC(CCO[Si](C)(C)C(C)(C)C)(C(=O)CC(O)Cc2ccccc2)CC1
Reaction #8867
tert-Butyl 4-(4-phenyl-3-hydroxy-1-oxobut-1-yl)-4-(2-(tert-butyldimethylsilyloxy)eth-1-yl)piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=CCc1ccccc1
Reaction #56123
phenylacetaldehyde
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
c1ccc(CCNCCc2ccccc2)cc1
Reaction #57343
compound D
Ausbeute 11.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(Nc1ccccc1)N1CCN(CCc2ccccc2)CC1
Reaction #68895
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
c1ccc(Cc2nc3cc(-c4nc5ccccc5o4)ccc3n2C2CCOCC2)cc1
Reaction #161416
title compound
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CN1CCN(C2CCC(n3nc(-c4ccc(C(NCCc5ccccc5)c5ccccc5)cc4)c4c(N)ncnc43)CC2)CC1
Reaction #176278
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Nc1ccccc1)N1CCN(CCc2ccccc2)CC1
Reaction #188947
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=c1[nH]c2ncnc(N3CCC(NCCc4ccccc4)CC3)c2[nH]1
Reaction #199558
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1ccc(CC2SCCCS2)cc1
Reaction #201936
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1ccc(CCN2CCCc3ccccc32)cc1
Reaction #202144
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])CC(O)Cc1ccccc1
Reaction #216166
desired product
Ausbeute 80.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CCOP(=O)(OCC)C(Cc1ccccc1)NS(=O)(=O)c1cccs1
Reaction #229037
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#CC(Cc1ccccc1)Nc1ccc(C(O)(C(F)(F)F)C(F)(F)F)cc1
Reaction #235589
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=CCc1ccccc1
Reaction #247941
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
NC(Cc1ccccc1)C(=O)O
Reaction #252399
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1nc(N2CCCC(CCc3ccccc3)C2=O)sc1C(=O)NCc1ccccc1
Reaction #265250
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1cccc2c1C(=O)NC1CN(CCc3ccccc3)CC21
Reaction #270801
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)C=Cc1ccc2c(c1)C(=O)NC1(CCN(CCc3ccccc3)CC1)O2
Reaction #273180
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C=C(Br)CC(O)Cc1ccccc1
Reaction #281165
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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