部分構造検索

Oc1cccc(O)c1

COc1ccc(CNc2ccc(Cl)cc2C(O)c2ccccc2Cl)c(OC)c1
Reaction #1868
5-chloro-α-(2-chlorophenyl)-2-(2,4-dimethoxybenzyl)aminobenzyl alcohol
収率 96.1%DOI: 10.6084/m9.figshare.5104873.v1
COCCOc1cc2nncc(Oc3cc(O)c(C)cc3F)c2cc1OC
Reaction #7589
4-(2-fluoro-5-hydroxy-4-methylphenoxy)-6-methoxy-7-(2-methoxyethoxy)cinnoline
収率 46.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cncnc2)cc1/C=C/C(=O)c1ccc(C(=O)O)cc1
Reaction #10734
title compound
収率 26.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1nnn(-c2ccc(O)cc2O)c1-c1ccc(F)cc1
Reaction #40718
1-(2,4-Dihydroxy-phenyl)-5-(4-fluoro-phenyl)-1H-[1,2,3]triazole-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nnn(-c2ccc(O)cc2O)c1-c1ccc(F)cc1
Reaction #40719
1-(2,4-Dihydroxy-phenyl)-5-(4-fluoro-phenyl)-1H-[1,2,3]triazole-4-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #42023
crude crystals
収率 72.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CC(c3cccc(F)c3F)=CC[C@@H](NC(=O)OCc3ccccc3)C2=O)c(OC)c1
Reaction #42664
title compound
収率 57.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CC=C(c2cccc(F)c2F)CNC1=O)OCc1ccccc1
Reaction #42665
title compound
収率 66.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c2c(CNC(=O)OC(C)(C)C)ncc(C(=O)O)c2c1
Reaction #42906
1-(tert-butoxycarbonylamino-methyl)-6,8-dimethoxy-isoquinoline-4-carboxylic acid
収率 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2nnc3sc(-c4ccc(C)c([N+](=O)[O-])c4)nn23)cc(OC)c1OC
Reaction #43303
title compound
収率 87.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2nnc3sc(-c4ccc5nc[nH]c5c4)nn23)cc(OC)c1OC
Reaction #43305
title compound
収率 17.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2nnc3sc(-c4ccc(N5CCOCC5)cc4)nn23)cc(OC)c1OC
Reaction #43306
title compound
収率 24.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(OC2=CC(=O)N([C@@H](CC3CCCC3)C(=O)Nc3ccn(CC(C)(C)O)n3)C2)c1Cl
Reaction #47265
(S)-2-[4-(2-chloro-3-methoxy-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-3-cyclopentyl-N-[1-(2-hydroxy-2-methyl-propyl)-1H-pyrazol-3-yl]-propionamide
収率 54.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CC(c3cccc(F)c3F)=CC[C@@H](NC(=O)OCc3ccccc3)C2=O)c(OC)c1
Reaction #48408
title compound
収率 57.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CC=C(c2cccc(F)c2F)CNC1=O)OCc1ccccc1
Reaction #48409
title compound
収率 66.4%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #61881
crude crystals
収率 72.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(O)c1C(C)(C)O
Reaction #66669
2-(1-Hydroxy-1-methyl-ethyl)-3-methoxy-phenol
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(O)c1C(C)C
Reaction #66670
2-Isopropyl-3-methoxy-phenol
収率 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc(C(=O)OC(C)(C)C)cc(OCC)c1-c1ccc(C(=O)OC)cc1
Reaction #66760
4-tert-Butyl 4′-methyl 2,6-diethoxybiphenyl-4,4′-dicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc(C(=O)O)cc(OCC)c1-c1ccc(C(=O)OC)cc1
Reaction #66761
2,6-Diethoxy-4′-(methoxycarbonyl)biphenyl-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
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