子结构搜索

CC=CCCl

Brc1ccc(-c2ccc(-c3ccc(Br)cc3)o2)cc1

2,5-Bis(p-bromophenyl) furan

DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)c1cc(CC)c2c(F)c(N3CCN(C)CC3)c(F)c(F)n2c1=O

DOI: 10.6084/m9.figshare.5104873.v1

O=C(C=Cc1cnc2ccccc2c1)NCCCSc1ccncc1

desired compound

收率 83.8%DOI: 10.6084/m9.figshare.5104873.v1

Cc1cc(=O)oc2c(C=CCCl)c(O)ccc12

Reaction #53759

desired compound

DOI: 10.6084/m9.figshare.5104873.v1

NC1(CP(O)O)C=CC(Cl)=CC1

Reaction #54257

1-amino-p-chlorophenylmethanephosphonous acid

DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)c1ccc(OCC=C(C)C)cc1

Reaction #69653

ethyl 4-(3-methyl-but-2-enyloxy)-benzoate

收率 95.2%DOI: 10.6084/m9.figshare.5104873.v1

O=C1C=CC(=O)C2C1C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl

Reaction #74961

1,2,3,4,9,9-hexachloro-1,4,4a,8a-tetrahydro-1,4-methanonaphthalene-5,8-dione

收率 64.0%DOI: 10.6084/m9.figshare.5104873.v1

CC(C)(C)C1=CC(=O)C2C(C1=O)C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl

Reaction #74963

6-tert-butyl-1,2,3,4,9,9-hexachloro-1,4,4a,8a-tetrahydro-1,4methanonaphthalene-5,8-dione

DOI: 10.6084/m9.figshare.5104873.v1

O=S(=O)(c1ccccc1)c1cc(O)c2c(c1O)C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl

Reaction #74964

1,2,3,4,9,9-hexachloro-1,4-dihydro-6-(phenylsulfonyl)-1,4-methanonaphthalene-5,8-diol

DOI: 10.6084/m9.figshare.5104873.v1

Oc1cc(Cl)c(O)c2c1C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl

Reaction #74966

1,2,3,4,6,9,9-heptachloro-1,4-dihydro-1,4-methanonaphthalene-5,8-diol

DOI: 10.6084/m9.figshare.5104873.v1

CC(C)(C)c1cc(O)c2c(c1O)C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl

Reaction #74968

DOI: 10.6084/m9.figshare.5104873.v1

O=C1CCC(=O)C2C1C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl

Reaction #74969

1,2,3,4,9,9-hexachloro-1,4,4a,6,7,8a-hexahydro-1,4-methanonaphthalene-5,8-dione

DOI: 10.6084/m9.figshare.5104873.v1

O=C1CC(S(=O)(=O)c2ccccc2)C(=O)C2C1C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl

Reaction #74970

1,2,3,4,9,9-hexachloro-1,4,4a,6,7,8a-hexahydro-6-phenylsulfonyl-1,4-methanonaphthalene-5,8-dione

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

CCCCSC1CC(=O)C2C(C1=O)C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl

Reaction #74971

6-butylthio-1,2,3,4,9,9-hexachloro-1,4,4a,6,7,8a-hexahydro-1,4-methanonaphthalene-5,8-dione

DOI: 10.6084/m9.figshare.5104873.v1

O=C1C2OC2C(=O)C2C1C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl

Reaction #74972

1,2,3,4,9,9-hexachloro-6,7-epoxy-1,4,4a,6,7,8a-hexahydro-1,4-methanonaphthalene-5,8-dione

DOI: 10.6084/m9.figshare.5104873.v1

CC1=CC(=O)C2C(C1=O)C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl

Reaction #74973

1,2,3,4,9,9-hexachloro-1,4,4a,8a-tetrahydro-6-methyl-1,4-methanonaphthalene-5,8-dione

DOI: 10.6084/m9.figshare.5104873.v1

N#CC1CCC2C(C1)C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl

Reaction #74975

DOI: 10.6084/m9.figshare.5104873.v1

$C(=C\c1nc2ccccc2n1-c1cccnc1)/c1ccccc1$

Reaction #79145

收率 34.0%DOI: 10.6084/m9.figshare.5104873.v1

CC(C)/C=C/c1nc2ccccc2n1-c1ccccn1.Cl

Reaction #79178

titled compound

DOI: 10.6084/m9.figshare.5104873.v1

FC(F)(F)c1ccc2c(c1)nc(/C=C/c1ccccc1)n2-c1ccccn1

Reaction #79196

titled compound

DOI: 10.6084/m9.figshare.5104873.v1

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