部分構造検索

228205

C/C=C/c1cc(F)c(F)c(F)c1

Reaction #44599

収率 84.1%DOI: 10.6084/m9.figshare.5104873.v1

C[C@H](O)[C@@H](O)c1cc(F)c(F)c(F)c1

Reaction #44600

DOI: 10.6084/m9.figshare.5104873.v1

C/C=C/c1cc(F)c(F)c(F)c1

Reaction #44631

収率 84.1%DOI: 10.6084/m9.figshare.5104873.v1

C[C@H](O)[C@@H](O)c1cc(F)c(F)c(F)c1

Reaction #44632

DOI: 10.6084/m9.figshare.5104873.v1

N#CC=Cc1ccc(Cl)c(F)c1

Reaction #51193

DOI: 10.6084/m9.figshare.5104873.v1

COc1c(C(=O)NNC(=O)OC(C)(C)C)ccc2c1c(/C=C/c1cccc(F)c1)nn2C(c1ccccc1)(c1ccccc1)c1ccccc1

Reaction #62331

収率 112.0%DOI: 10.6084/m9.figshare.5104873.v1

$C/C(=C\c1cc(F)c(Oc2ccc(S(=O)(=O)NCCOCCOCCOCCn3cc(CO)nn3)cc2)c(F)c1)C(=O)N=C(N)N$

Reaction #73973

収率 30.0%DOI: 10.6084/m9.figshare.5104873.v1

CC(=O)C=Cc1cc(F)ccc1Cl

Reaction #77474

4-(2-chloro-5-fluorophenyl)-3-buten-2-one

DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)/C=C/c1ccc(OCc2ccccc2)c(F)c1

Reaction #91120

収率 22.0%DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)CCc1ccc(O)c(F)c1

Reaction #91121

収率 105.1%DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)/C(C)=C/c1ccc(OC)c(F)c1

Reaction #91156

収率 99.5%DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)C(C)Cc1ccc(OC)c(F)c1

Reaction #91157

収率 100.7%DOI: 10.6084/m9.figshare.5104873.v1

CC(=Cc1c(F)c(F)cc(F)c1F)[N+](=O)[O-]

Reaction #156512

designed compound

収率 91.1%DOI: 10.6084/m9.figshare.5104873.v1

CC(=O)Oc1ccc(C=Cc2cc(F)cc(OCc3ccccc3)c2)cc1

Reaction #166066

desired product

収率 88.0%DOI: 10.6084/m9.figshare.5104873.v1

CC(=O)Oc1ccc(C=Cc2cc(O)cc(F)c2)cc1

Reaction #166067

4′-acetoxy-3-fluoro-5-hydroxystilbene

収率 61.2%DOI: 10.6084/m9.figshare.5104873.v1

CCCc1cccc(F)c1F

Reaction #173207

DOI: 10.1039/C8SC04228D

C=Cc1cc(F)ccc1C#N

Reaction #177855

DOI: 10.1039/C8SC04228D

C=Cc1cc(F)ccc1Br

Reaction #183284

DOI: 10.1039/C8SC04228D

CS(=O)c1ccc(C2=C(c3cccc(F)c3)C(=O)C(C)(C)O2)cc1F

Reaction #187147

DOI: 10.1039/C8SC04228D

O=C(O)CCCCc1ccc(Br)c(F)c1

Reaction #190821

DOI: 10.1039/C8SC04228D

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