Поиск подструктуры

945928

COc1ccc(O)c(OC)c1OC
Reaction #3779
2,3,4-trimethoxyphenol
Выход 51.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C=O)c(O)c1O
Reaction #9403
purple solid
Выход 73.0%DOI: 10.6084/m9.figshare.5104873.v1
[Li][c]1cc(OC)c(OC)c(OC)c1
Reaction #9406
3,4,5-trimethoxyphenyllithum
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc([C@@H]2c3cc4c(cc3[C@H](OC(=O)CCC(=O)O)[C@H]3COC(=O)[C@H]23)OCO4)cc(OC)c1OC
Reaction #44940
succinylpodophyllotoxin
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C2CCC(OC)O2)cc(OC)c1OC
Reaction #50766
2-(3,4,5-trimethoxyphenyl)-5 -methoxytetrahydrofuran
Выход 27.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Br)cc(OC)c1OC
Reaction #52140
18
Выход 79.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(P(c2ccccc2)c2ccccc2)cc(OC)c1OC
Reaction #52141
19
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C=O)cc(OC)c1OC
Reaction #56125
3,4,5-trimethoxybenzaldehyde
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)CCCCC2(O)c1cc(OC)c(OC)c(OC)c1
Reaction #62224
32
Выход 49.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCC(=O)c1ccc(OC)c(OC)c1OC
Reaction #62236
55
Выход 72.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)CCC(=O)O)c(OC)c1OC
Reaction #62237
56
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cc2cnc(N)nc2N)c2c(c1OC)OCC=C2.O=C(O)/C=C\C(=O)O
Reaction #62720
title compound
Выход 94.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cc2cnc(N)nc2N)c2c(c1OC)OCC=C2.O=C(O)CC(O)(CC(=O)O)C(=O)O
Reaction #62721
title compound
Выход 99.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cc2cnc(N)nc2N)c2c(c1OC)OCC=C2.O=C1O[C@H]([C@@H](O)CO)C([O-])=C1O
Reaction #62722
title compound
Выход 97.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cc2cnc(N)nc2N)c2c(c1OC)OC(C)=CC2
Reaction #62726
title compound
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cc2cnc(N)nc2N)c2c(c1OC)OC(C)C=C2
Reaction #62731
title compound
Выход 37.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C=O)c2c(c1OC)OCC=C2
Reaction #62739
7,8-Dimethoxy-5-formyl-2H-1-benzopyran
Выход 100.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cc2c[n+]([O-])c(N)nc2N)c2c(c1OC)OCC=C2
Reaction #62743
2,4-Diamino-5-(7,8-dimethoxy-2H-1-benzopyran-5-ylmethyl)pyrimidine-1-oxide
DOI: 10.6084/m9.figshare.5104873.v1
COCC(C#N)=Cc1cc(OC)c(OC)c2c1C=CCO2
Reaction #62744
amber oil
Выход 73.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C#N)=Cc1cc(OC)c(OC)c2c1C=CCO2
Reaction #62747
orange solid
Выход 66.9%DOI: 10.6084/m9.figshare.5104873.v1
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