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945223

COc1ccc(C=O)cc1-c1ccnc(Cl)n1
Reaction #43240
3-(2-chloropyrimidin-4-yl)4-methoxybenzaldehyde
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OC)c(-c2cc(C(F)(F)F)cc3[nH]ncc23)c1
Reaction #86368
title compound
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C=O)cc1-c1ccc(F)c(S(C)(=O)=O)c1
Reaction #155790
3-(4-fluoro-3-(methylsulfonyl)phenyl)-4-methoxybenzaldehyde
Ausbeute 108.1%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1c(-c2ccc(F)cc2)oc2ccc(-c3cc(C(=O)O)ccc3OC)c(F)c12
Reaction #205048
DOI: 10.1039/C8SC04228D
COC(=O)c1cc2c(c(-c3ccc(OC)c(Cl)c3)c1)OC(F)(F)O2
Reaction #210140
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c[nH]c2c(-c3cc(C(C)=O)c(C)cc3OCC3CC3)ncnc12
Reaction #230322
DOI: 10.1039/C8SC04228D
CCN1C(=O)CC(C)(C)c2cc(C)c(-c3cc(C=O)ccc3OC)cc21
Reaction #274873
DOI: 10.1039/C8SC04228D
COc1ccc(C=O)cc1-c1c(C)cccc1C
Reaction #394923
DOI: 10.1039/C8SC04228D
COc1ccc(C=O)cc1-c1ccc2oc(C)nc2c1
Reaction #547307
title compound
Ausbeute 89.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1cncc(-c2cc(C=O)ccc2OC)c1
Reaction #547339
title compound
Ausbeute 88.6%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)c1cc(-c2cc(C=O)ccc2OC(F)(F)F)c2c(c1)C(C)(C)CO2
Reaction #547475
3-(3,3-dimethyl-5-propionyl-2,3-dihydro-benzofuran-7-yl)-4-trifluoromethoxy-benzaldehyde
Ausbeute 73.6%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #576001
solid
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
COC1(c2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)C=CC=C(C=O)C1
Reaction #576016
3-(3,5-di-t-butyl-4-hydroxyphenyl)-3-methoxybenzaldehyde
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(-c2ccccn2)c(OC)cc1Cl
Reaction #609324
title compound
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1c(-c2ccc(F)cc2)oc2ccc(-c3cc(C(=O)O)ccc3OC)cc12
Reaction #642289
3-(2-(4-fluorophenyl)-3-(methylcarbamoyl)benzofuran-5-yl)-4-methoxy benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)O)cc1B(O)O
Reaction #691402
2-methoxy-5-carboxyphenylboronic acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)N(C)C)cc1B(O)O
Reaction #691403
2-methoxy-5-dimethylcarbamoylphenylboronic acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C=O)cc1-c1ccc(C(F)(F)F)cc1CN1C(=O)O[C@H](c2cc(C(F)(F)F)cc(C(F)(F)F)c2)[C@@H]1C
Reaction #694263
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cc2ccc(-n3cccn3)cc2)c(OC)cc1O
Reaction #716508
title compound
Ausbeute 54.6%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1c(-c2ccc(F)cc2)oc2ccc(-c3cc(C(=O)O)ccc3OC)cc12
Reaction #764804
DOI: 10.1039/C8SC04228D
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