Substructure Search

C1=CC2CCC1C2

C=C(C)CC(C)(O)C1C2C=CC(C2)C1(C)C
Reaction #54465
oil
Yield 106.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(c2ccc(O)c(C)c2)C2CC3CC2CC3c2ccc(C3CC4CC3CC4C(c3ccc(O)c(C)c3)c3ccc(O)c(C)c3)cc2)ccc1O
Reaction #68720
4,4′-((5-(4-(5-(bis(4-hydroxy-3-methylphenyl)methyl)bicyclo[2.2.1]heptan-2-yl)phenyl) bicyclo[2.2.1]heptan-2-yl)methylene)bis(2-methylphenol)
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C2CC3CC2CC3C(c2ccc(O)c(C)c2)c2ccc(O)c(C)c2)ccc1O
Reaction #68721
4,4′-((5-(4-hydroxy-3-methylphenyl)bicyclo[2.2.1]heptan-2-yl)methylene)-bis(2-methylphenol)
Yield 54.0%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
Yield 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
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
crystals
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
Yield 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
O=C1c2ccccc2C(=O)C2C1C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74974
1,2,3,4,11,11-hexachloro-1,4,4a,9a-tetrahydro-1,4-methanoanthracene-9,10-dione
DOI: 10.6084/m9.figshare.5104873.v1
N#CC1CCC2C(C1)C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74975
crude adduct
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)CC(C)(O)C1C2C=CC(C2)C1(C)C
Reaction #94408
oil
Yield 106.5%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #95322
exo-2,3-dicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1(C(=O)O)CC2C=CC1C2
Reaction #96218
2,2-dicarboxy-5-norbornene
Yield 89.6%DOI: 10.6084/m9.figshare.5104873.v1
OC1(CCCCCC2CC3CC2C2C4C=CC(C4)C32)CCCC1
Reaction #173335
DOI: 10.1039/C8SC04228D
COC1C2C=CC1C1N=NC21
Reaction #203319
DOI: 10.1039/C8SC04228D
CC(=O)C1=CC23C=CC=CC2CC1C3
Reaction #212687
DOI: 10.1039/C8SC04228D
Page 1Next