An 65 Reaktionen beteiligt

628

COc1ccccc1N1CCN(C(=O)OC(C)(C)C)CC1
Reaction #751
Ausbeute 11.2%750 AstraZeneca ELN dataset
COc1ccccc1C1CC(C)CCC1=O
Reaction #54760
2-Methoxyphenyl-4-methylcyclohexanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CCCCOc1ccccc1OC
Reaction #166169
1-Butoxy-2-methoxybenzene
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1ccc(C(=O)CCCCCBr)cc1Cl
Reaction #375632
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1ccccc1-c1ccc2ccccc2c1
Reaction #383389
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1ccc(C(=O)C=CC(=O)O)cc1Cl
Reaction #398056
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1ccccc1Cl
Reaction #406387
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1ccc(C(C)=O)cc1Cl
Reaction #430249
3-chloro-4-methoxyacetophenone
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
COc1ccc(C(=O)CCCCCBr)cc1Cl
Reaction #431442
6-bromo-1-(3-chloro-4-methoxyphenyl)-1-hexanone
Ausbeute 32.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CCCCCCNc1ccccc1OC
Reaction #499961
title compound
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
CCOC(=O)C(C#N)c1ccccc1OC
Reaction #500017
desired product
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
COc1cccc(C2CCCCNC2=O)c1
Reaction #516248
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
CCC1(c2cccc(OC)c2)CCCCNC1=O
Reaction #516249
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
COc1ccc(-c2ccc(C)cc2)cc1
Reaction #554426
4'-methoxy-4-methylbiphenyl
Ausbeute 42.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_10
COc1ccccc1C(C)C(=O)c1ccccc1
Reaction #682534
2-(2′-Methoxyphenyl)-1-phenyl-1-propanone
Ausbeute 82.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
COc1ccccc1CC(C)=O
Reaction #682547
1-(2′-Methoxyphenyl)-2-propanone
Ausbeute 179.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
COc1ccc(C23CC4CC(CC(C4)C2)C3)cc1Cl
Reaction #716733
1-(3-chloro-4-methoxyphenyl)adamantane
Ausbeute 84.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
CCOC(=O)C(C#N)c1ccccc1OC
Reaction #789553
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COc1ccc(S(=O)(=O)Cl)cc1Cl
Reaction #903110
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCC1(c2cccc(OC)c2)CCCCN(C)C1=O
Reaction #935591
3-ethylhexahydro-3-(3 -methoxyphenyl)-1-methyl-2H-azepin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_10
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