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Cc1cc(O)cc(O)c1

COc1cc(C)cc(OC)c1N=C1CCCCC1
Reaction #3013
N-cyclohexylidene-2,6-dimethoxy-4-methylaniline
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C)cc(OC)c1NC1C2CC3CC(C2)CC1C3
Reaction #3016
N-(2-adamantyl)-2,6-dimethoxy-4-methylaniline
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CNc1c(OC)cc(C)cc1OC
Reaction #3017
N-methyl-2,6-dimethoxy-4-methylaniline
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C)cc(OC)c1NC(=O)CC(C)C
Reaction #3018
N-(2,6-dimethoxy-4-methylphenyl)isovaleramide
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #7832
desired intermediate
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #7833
desired intermediate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(/C=C\c2cc(OC)c(OC)c(OC)c2)cc1O
Reaction #8837
combretastatin A-4
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(COc2cc(NC(=O)c3ccc(N4CCN(C5CC5)CC4)cc3)[nH]n2)cc(OC)c1
Reaction #45096
title compound
Ausbeute 3.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Oc2ccc(S(C)(=O)=O)cc2)cc(O[C@@H](C)CO[Si](C)(C)C(C)(C)C)c1
Reaction #48767
title compound
Ausbeute 87.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(O)cc(Oc2ccc(S(C)(=O)=O)cc2)c1
Reaction #48768
title compound
Ausbeute 100.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C2OCCO2)cc(OC)c1Br
Reaction #52980
4-bromo-3,5-dimethoxybenzaldehyde ethylene acetal
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CCC(=O)O)cc(OC)c1OC
Reaction #64693
3-(3,4,5-trimethoxyphenyl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(OC)cc(OCc2ccccc2)c1
Reaction #66933
methyl 3-(benzyloxy)-5-methoxybenzoate
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCc2ccccc2)cc(C(=O)O)c1
Reaction #66934
162
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2ccc(NC(=O)c3ccc(-c4c(Cl)c(OC)cc(OC)c4Cl)c4cccnc34)cc2)CC1
Reaction #71469
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)Nc3cnc[nH]3)c3ncccc23)c1Cl
Reaction #71475
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)Nc3ccc(CN4CCN(C)CC4)cn3)c3ncccc23)c1Cl
Reaction #71476
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(Cc2ccc(NC(=O)c3ccc(-c4c(Cl)c(OC)cc(OC)c4Cl)c4cccnc34)nc2)CC1
Reaction #71477
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CCN(Cc3ccc(NC(=O)c4ccc(-c5c(Cl)c(OC)cc(OC)c5Cl)c5cccnc45)nc3)CC2)cc1
Reaction #71478
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)Nc3ccc(CN4CCN(C)CC4)nc3)c3ncccc23)c1Cl
Reaction #71480
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
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