부분 구조 검색

6494

C[C@H](NC(=O)[C@@H]1CCCN1)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccc2c(c1)OCCO2
Reaction #41432
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OC)c2c1OCCCO2
Reaction #43297
intermediate 7
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
수율 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)O)ccc1OCc1ccccc1
Reaction #48269
4-benzyloxy-3-methoxy benzoic acid
수율 94.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)Nc2ccc(OC)c(OCc3ccccc3)c2)ccc1OCc1ccccc1
Reaction #48270
4-Benzyloxy-3-methoxy-N-(3-benzyloxy-4-methoxyphenyl)benzamide
수율 71.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(C)O)cc(Br)c1OC
Reaction #71254
1-(3-Bromo-4,5-dimethoxyphenyl)-1-ethanol
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(F)c(C(O)CN)cc1OC.Cl
Reaction #82963
α-(aminomethyl)-6-fluoro-3,4-dimethoxybenzyl alcohol hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc([C@@H]2c3cc4c(cc3[C@@H](O[C@@H]3O[C@@H]5CO[C@@H](C)O[C@H]5[C@H](O)[C@H]3O)[C@H]3COC(=O)[C@H]23)OCO4)cc(OC)c1O
Reaction #92883
Etoposide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)O)ccc1OC(C)C
Reaction #160173
4-isopropoxy-3-methoxy-benzoic acid
수율 90.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(O)c(C(=O)O)cc1OC
Reaction #165879
2-hydroxy-4,5-dimethoxybenzoic acid
수율 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(O)c(C(=O)O)cc1OC
Reaction #165880
compound ( 2a )
수율 133.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(O)c(C(=O)O)cc1OC
Reaction #165881
compound ( 2a )
수율 73.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(O)c(C(=O)O)cc1OC
Reaction #165882
compound ( 2a )
수율 96.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(O)c(C(=O)Oc2ccccc2)cc1OC
Reaction #165883
phenyl 2-hydroxy-4,5-dimethoxybenzoate
수율 64.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(COc2nn(Cc3ccccc3)cc2CC(=O)O)ccc1OCc1nc(-c2ccccc2)oc1C
Reaction #172990
DOI: 10.1039/C8SC04228D
COc1ccc(COc2cccc3c2CN(C2CCC(=O)NC2=O)C3=O)cc1OC
Reaction #177179
DOI: 10.1039/C8SC04228D
COc1ccc(C(O)CNC(C)CCc2ccccc2)cc1OCCOC1CCCCO1
Reaction #179823
DOI: 10.1039/C8SC04228D
COc1cc(COc2nn(-c3ccccc3)cc2C=Cc2csc(C(C)(C)C)n2)ccc1OCc1nc(-c2ccc(CC(=O)O)cc2)oc1C
Reaction #181816
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1cnccc1OCc1ccc2c(c1)OCO2
Reaction #184426
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc(OC)c(OCCCN2CCOCC2)cc1N
Reaction #187126
DOI: 10.1039/C8SC04228D
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