部分構造検索

Cc1ccc(O)cc1

$COc1cc(/C=C\c2ccc(Cl)c([N+](=O)[O-])c2)cc(OC)c1OC$

intended compound

収率 50.9%DOI: 10.6084/m9.figshare.5104873.v1

$COc1cc(/C=C\c2ccc(C)c([N+](=O)[O-])c2)cc(OC)c1OC$

intended compound

収率 49.6%DOI: 10.6084/m9.figshare.5104873.v1

COc1ccc(C(CC(=O)O)N2C(=O)c3ccccc3C2=O)cc1OC1CCCC1

3-(3-cyclopentyloxy-4-methoxy-phenyl)-3-phthalimidopropanoic acid

収率 68.0%DOI: 10.6084/m9.figshare.5104873.v1

CN1CCN(CC(c2ccc(OCc3ccc(C(F)(F)F)cc3)c(F)c2)C2(O)CCCCC2)CC1.Cl.Cl

Reaction #57124

1-[1-(3-fluoro-4-{[4-(trifluoromethyl)benzyl]oxy}phenyl)-2-(4-methylpiperazin-1-yl)ethyl]cyclohexanol Dihydrochloride

DOI: 10.6084/m9.figshare.5104873.v1

Cc1oc(-c2ccc(C(F)(F)F)cc2)nc1-c1ccc(-c2cc(Br)c(OCC(=O)O)c(Br)c2)cc1

Reaction #75937

DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)C(Cc1ccccc1)Oc1c(Br)cc(-c2ccc(-c3nc(-c4ccc(C(F)(F)F)cc4)oc3C)cc2)cc1Br

Reaction #75938

DOI: 10.6084/m9.figshare.5104873.v1

COc1ccccc1OCCCN(C)CCC(C#N)(c1cc(OC)c(OC)c(OC)c1)C(C)C

Reaction #93370

desired compound

DOI: 10.6084/m9.figshare.5104873.v1

COc1cc(C(C#N)(CCCN(C)CCCOc2cccc(CO)c2)C(C)C)cc(OC)c1OC

Reaction #93374

desired compound

収率 25.7%DOI: 10.6084/m9.figshare.5104873.v1

CCc1ccc(/C(=C/C2CCCC2)c2ccc(O)c(Cl)c2)nc1OC

Reaction #157771

2-chloro-4-[(E)-2-cyclopentyl-1-(5-ethyl-6-methoxypyridin-2-yl)ethenyl]phenol

収率 99.0%DOI: 10.6084/m9.figshare.5104873.v1

CC[C@@H](NC(=O)N1CC(=O)N(Cc2c(OC)cc(OC)cc2OC)C[C@@H](Cc2cc(Cl)ccc2OC)C1=O)c1cc(C(=O)OC(C)(C)C)ccn1

Reaction #167761

tert-butyl 2-[(1R)-1-({[(6R)-6-(5-chloro-2-methoxybenzyl)-3,7-dioxo-4-(2,4,6-trimethoxybenzyl)-1,4-diazepan-1-yl]carbonyl}amino)propyl]isonicotinate

収率 71.5%DOI: 10.6084/m9.figshare.5104873.v1

CC(C)Oc1cc2c(cc1Br)C(C)CNCC2

Reaction #171268

収率 76.6%DOI: 10.6084/m9.figshare.5104873.v1

CCCOc1ccc(CN2CCC(C(O)(c3ccc(Cl)cc3)c3ccc(OC(F)(F)F)cc3)CC2)cc1

Reaction #174959

DOI: 10.1039/C8SC04228D

CC1(C)CC(=C(c2ccc(O)cc2)c2ccc(C(=O)O)cc2)CC(C)(C)O1

Reaction #183394

DOI: 10.1039/C8SC04228D

COc1ccc(COC(c2ccccc2)(c2ccc(OC)cc2)C2CNCC2O)cc1

Reaction #185205

DOI: 10.1039/C8SC04228D

COc1ccc(Cn2ccc3c(O)c(CO)cnc3c2=O)cc1

Reaction #200244

DOI: 10.1039/C8SC04228D

N#Cc1ccc(Oc2ccc(C=C3SC(=S)NC3=O)cc2F)c(C(F)(F)F)c1

Reaction #209762

DOI: 10.1039/C8SC04228D

COc1cc(C(=O)OCCN(CCOC(=O)c2cc(OC)c(OC)c(OC)c2)CCS(=O)(=O)O)cc(OC)c1OC

Reaction #215390

N,N-di-[2-(3,4,5-trimethoxybenzoyloxy)ethyl]taurine

DOI: 10.6084/m9.figshare.5104873.v1

COCCOCOc1c(OC)cc(C=CC=CC(=O)NCCN2CCC(c3c[nH]c4ccccc34)CC2)cc1OC

Reaction #225040

DOI: 10.1039/C8SC04228D

N#Cc1ccc(N(Cc2ccc(O)cc2)c2ccncc2)cc1

Reaction #250122

DOI: 10.1039/C8SC04228D

Fc1cc(C2OCCCO2)ccc1-c1nc2ccc(C3(c4ccc(OCc5ccccc5)cc4)CC3)nc2s1

Reaction #250685

DOI: 10.1039/C8SC04228D

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