An 84 Reaktionen beteiligt

7969

Cc1oc(-c2ccccc2)nc1CCO
Reaction #4497
2-(5-methyl-2-phenyl-4-oxazolyl) ethanol
Ausbeute 96.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Cc1oc(-c2ccccc2)nc1CCOc1ccc(C#N)cc1
Reaction #4504
4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]benzonitrile
Ausbeute 77.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Cc1oc(-c2ccccc2)nc1CCO
Reaction #76187
compound [ 6 ]
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1oc(-c2ccccc2)nc1CCOc1cncc(N2CCNCC2)n1
Reaction #186842
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1oc(-c2ccccc2)nc1CCO
Reaction #191682
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1oc(-c2ccccc2)nc1CCOc1cccc(C=O)c1
Reaction #212427
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)c1ccc(OCCc2nc(-c3ccccc3)oc2C)cc1
Reaction #216705
solid
Ausbeute 77.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
Cc1oc(-c2ccccc2)nc1CCOc1ccc([N+](=O)[O-])cn1
Reaction #246913
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1oc(-c2ccccc2)nc1CCOc1ccc([N+](=O)[O-])cn1
Reaction #320454
2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]-5-nitropyridine
Ausbeute 49.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
Cc1oc(-c2ccccc2)nc1CCOc1ccc(C=O)cc1
Reaction #363266
4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cc1cccc(C)c1OCCc1nc(-c2ccccc2)oc1C
Reaction #390133
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1oc(-c2ccccc2)nc1CCOCCCCCBr
Reaction #403466
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1oc(-c2ccccc2)nc1CCOc1ccc(Cn2cc(CCC(=O)O)c(-c3ccccc3)c2)cc1
Reaction #437224
3-[1-[4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]benzyl]-4-phenyl-3-pyrrolyl]propionic acid
Ausbeute 66.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
Cc1oc(-c2ccccc2)nc1CCOc1ccc(NC(=O)OC(C)(C)C)cc1
Reaction #439623
title compound
Ausbeute 79.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
Cc1oc(-c2ccccc2)nc1CCOc1ccc(Nc2ccccc2)cc1
Reaction #439626
title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
Cc1oc(-c2ccccc2)nc1CCO
Reaction #440852
2-(5-Methyl-2-phenyl-4-oxazolyl)ethanol
Ausbeute 118.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
Cc1oc(-c2ccccc2)nc1CCOCCCCCBr
Reaction #520064
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12
Cc1cccc(C)c1OCCc1nc(-c2ccccc2)oc1C
Reaction #566311
title compound
Ausbeute 32.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_11
Cc1cccc(OCCc2nc(-c3ccccc3)oc2C)c1
Reaction #566331
title compound
Ausbeute 78.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_11
CCOC(=O)C(Cc1ccc(OCCc2nc(-c3ccccc3)oc2C)c(OC)c1)OCC
Reaction #566370
[rac]-2-ethoxy-3-{3-methoxy-4-[2-(5-methyl-2-phenyl-oxazol-4-yl)-ethoxy]-phenyl}-propionic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_11
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