4-bromo-3,5-dimethylisoxazole

Cc1noc(C)c1-c1ccccc1C=C1c2ccccc2CCc2ccccc21
Reaction #292366
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1noc(C)c1-c1ccnc(Cl)c1
Reaction #328879
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CCC(CC)c1cc(C)nn2c(-c3c(C)noc3C)c(C)nc12
Reaction #782663
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCOC(=O)Cc1cccc(Oc2ccc(-c3c(C)noc3C)cc2CN2C(=O)O[C@H](c3ccccc3)[C@@H]2C)c1
Reaction #972541
{3-[4-(3,5-Dimethyl-isoxazol-4-yl)-2-((4S,5R)-4-methyl-2-oxo-5-phenyl-oxazolidin-3-ylmethyl)-phenoxy]-phenyl}-acetic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
Cc1noc(C)c1B(O)O
Reaction #1009444
(3,5-Dimethyl-1,2-oxazol-4-yl) boronic acid
Ausbeute 12.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
CCOC(=O)Cc1cccc(Oc2ccc(-c3c(C)noc3C)cc2CN2C(=O)OC(c3ccccc3)C2C)c1
Reaction #1312830
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
Cc1noc(C)c1-c1ccnc(Cl)c1
Reaction #1321054
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
Cc1noc(C)c1-c1ccnc(Cl)c1
Reaction #1509595
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_01
CCC(CC)c1cc(C)nn2c(-c3c(C)noc3C)c(C)nc12
Reaction #1519902
title compound
Ausbeute 23.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_11
Cc1noc(C)c1-c1cc(C=O)c2occc2c1
Reaction #1671965
5-(3,5-Dimethyl-isoxazol-4-yl)-benzofuran-7-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_08
Cc1noc(C)c1-c1ccnc(Cl)c1
Reaction #2146844
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_10
Cc1noc(C)c1-c1ccccc1C=C1c2ccccc2CCc2ccccc21
Reaction #2305900
title compound
Ausbeute 2.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_08