Busqueda de Subestructura

88722

CN(C)C1C(O)=C(C(N)=O)C(=O)C2(O)C(O)=C3C(=O)c4c(O)ccc(Br)c4CC3CC12.O=S(=O)(O)O
Reaction #6539
pure product
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](O)[C@H](O)[C@@H](O)[C@@H](O)C=O
Reaction #10222
L-Rhamnose
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
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
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
Cc1ccc(C)c(O)c1C
Reaction #94078
2,3,6-trimethylphenol
Rendimiento 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=CCC(C)C(C)C1=O
Reaction #94079
2,5,6-trimethyl-2-cyclohexen-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CC1=CCC(C)C(C)C1=O
Reaction #94080
2,5,6-trimethyl-2-cyclohexen-1-one
Rendimiento 47.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1=CCC(C)C(C)C1=O
Reaction #94081
2,5,6-trimethyl-2-cyclohexen-1-one
Rendimiento 56.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C)c(O)c1C
Reaction #94082
2,3,6-trimethylphenol
Rendimiento 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CON(C)CC(=O)Nc1cc(N(C)C)c2c(c1O)C(=O)C1=C(O)C3(O)C(=O)C(C(N)=O)=C(O)C(N(C)C)C3CC1C2
Reaction #205141
DOI: 10.1039/C8SC04228D
Cc1nc(C(F)(F)F)ccc1C(=O)C1=C(O)C2CC2C(C)(S(C)=O)C1=O
Reaction #222274
DOI: 10.1039/C8SC04228D
CN(C)c1cc(NC(=O)C2CCCN2)c(O)c2c1CC1CC3C(N(C)C)C(O)=C(C(N)=O)C(=O)C3(O)C(O)=C1C2=O
Reaction #236399
DOI: 10.1039/C8SC04228D
CN(C)c1cc2nc(SCC(=O)OCc3ccccc3)oc2c2c1CC1CC3C(N(C)C)C(O)=C(C(N)=O)C(=O)C3(O)C(O)=C1C2=O
Reaction #287104
DOI: 10.1039/C8SC04228D
Reaction #310787
89
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C)c(N)c1C
Reaction #310788
2,3,6-trimethylaniline
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](N)c3ccccc3)C(=O)N2[C@H]1C(=O)O
Reaction #323604
Ampicillin
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C1C(O)=C(C(N)=O)C(=O)C2C(=O)C3=C(O)c4c(O)cccc4C(C)(O)C3CC21
Reaction #343706
12a-deoxytetracycline
Rendimiento 21.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(C(=O)c3ccccc31)C(=O)C1CC(Cl)=CCC1C2=O
Reaction #348339
9-chloro-6a,7,10,10atetrahydro-5,6,11,12-naphthacenetetraone
Rendimiento 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)[C@@H]1C(O)=C(C(N)=O)C(=O)[C@@]2(O)C(O)=C3C(=O)c4c(O)cccc4[C@@](C)(O)[C@H]3[C@H](O)[C@@H]12.[Mg]
Reaction #416098
magnesium oxytetracycline
DOI: 10.6084/m9.figshare.5104873.v1
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