子结构搜索

Cc1ccccc1O

CC(C)(C)OC(=O)N1CCCC1c1cc([N+](=O)[O-])c(N)cc1Oc1ccc(-c2ccccc2F)cc1
Reaction #41678
compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC1c1cc(N)c(N)cc1Oc1ccc(-c2ccccc2F)cc1
Reaction #41679
t-butyl 2-(4,5-diamino-2-((2′-fluorobiphenyl-4-yl)oxy)phenyl)pyrrolidine 1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C(C)C=CC(=O)c1cc(OC)ccc1OCC(C)C
Reaction #44923
ethyl 6-(2-isobutoxy-5-methoxyphenyl)-6-oxo-3-methylhexa-2,4-dienoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N(Cc1cc(C#N)cc(C(F)(F)F)c1)Cc1cc(C(F)(F)F)ccc1-c1cc(C(C)C)ccc1OC
Reaction #45349
methyl[3-cyano-5-(trifluoromethyl)benzyl]{[5′-isopropyl-2′-methoxy-4-(trifluoromethyl)biphenyl-2-yl]methyl}carbamate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N(Cc1cc(C(N)=O)cc(C(F)(F)F)c1)Cc1cc(C(F)(F)F)ccc1-c1cc(C(C)C)ccc1OC
Reaction #45352
methyl[3-(aminocarbonyl)-5-(trifluoromethyl)benzyl]{[5′-isopropyl-2′-methoxy-4-(trifluoromethyl)biphenyl-2-yl]methyl}carbamate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N(Cc1cc(C(=O)O)cc(C(F)(F)F)c1)Cc1cc(C(F)(F)F)ccc1-c1cc(C(C)C)ccc1OC
Reaction #45353
3-{[{[5′-isopropyl-2′-methoxy-4-(trifluoromethyl)biphenyl-2-yl]methyl}(methoxycarbonyl)amino]methyl}-5-(trifluoromethyl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cc(CN(Cc2cc(C(F)(F)F)ccc2-c2cc(C(C)C)ccc2OC)C(=O)OC)cc(C(F)(F)F)c1
Reaction #45354
methyl{[5′-isopropyl-2′-methoxy-4-(trifluoromethyl)biphenyl-2-yl]methyl}[3-(trifluoromethyl)-5-vinylbenzyl]carbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc(C(=O)N2Cc3ccc(C(=O)N4CCN(C(=O)OC(C)(C)C)CC4)cc3C2)c(O)cc1O
Reaction #69728
4-[2-(2,4-dihydroxy-5-isopropyl-benzoyl)-2,3-dihydro-1H-isoindole-5-carbonyl]-piperazine-1-carboxylic acid tert-butyl ester
收率 102.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C=Cc1ccc(-c2ccc(OCN3C(=O)c4ccccc4C3=O)c(C34CC5CC(CC(C5)C3)C4)c2)cc1
Reaction #70000
3-[3′-Adamantan-1-yl-4′-(1,3-dioxo-1,3-dihydroisoindol-2-ylmethoxy)-biphenyl-4-yl]acrylic acid tert-butyl ester
收率 55.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)/C=C/c1ccc(-c2ccc(OCN3C(=O)c4ccccc4C3=O)c(C34CC5CC(CC(C5)C3)C4)c2)cc1
Reaction #70001
(E)-3-[3′-Adamantan-1-yl-4′-(1,3-dioxo-1,3-dihydroisoindol-2-ylmethoxy)-biphenyl-4yl]-acrylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(c2cc(Cl)ccc2O)C1
Reaction #74589
title compound
收率 38.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(c2cc(Cl)ccc2O[Si](C)(C)C(C)(C)C)C1
Reaction #74590
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O.CCC[C@@H](NC(=O)N1C/C(=N/OCC)NC[C@H](Cc2cc(Cl)ccc2OC)C1=O)c1ccc(C(=O)O)c(N)c1
Reaction #167760
title compound
收率 175.8%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](NC(=O)N1CC(=NOc2ccccc2)NC[C@@H](Cc2cc(Cl)ccc2OC)C1=O)c1ccc(C(=O)O)c(N)c1.Cl
Reaction #167769
title compound
收率 161.7%DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@@H](NC(=O)N1CC(=NO)NC[C@H](Cc2cc(Cl)ccc2OC)C1=O)c1ccc(C(=O)O)c([N+](=O)[O-])c1.Cl
Reaction #167776
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@@H](NC(=O)N1CC(=NOCC)NC[C@@H](Cc2cc(Cl)ccc2OC)C1=O)c1ccc(C(=O)O)c(N)c1
Reaction #167778
title compound
收率 101.3%DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@@H](NC(=O)N1CC(=NOCC)NC[C@@H](Cc2cc(Cl)ccc2OC)C1=O)c1ccc(C(=O)O)c(N)c1.Cl.Cl
Reaction #167779
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(C)(C)CCC(=O)O)cc1C
Reaction #173249
DOI: 10.1039/C8SC04228D
CCOc1cc(C(C)(C)C)ccc1C1=NC(C)(c2ccc(Cl)cc2)C(C)(c2ccc(Cl)cc2)N1C(=O)c1ccco1
Reaction #176118
DOI: 10.1039/C8SC04228D
CCOC(=O)N1CCC(NC(=O)c2c[nH]c3c(-c4ccccc4OCC4CC4)ncnc23)CC1
Reaction #176134
DOI: 10.1039/C8SC04228D
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