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Depiction
Precursor
(1S,2S,4R,5S,7R)-4-methoxy-7-methyl-2-phenylmethoxy-6,8-dioxabicyclo[3.2.1]octane
C[C@@H]1[C@H]2[C@H](C[C@H]([C@@H](O1)O2)OC)OCC3=CC=CC=C3
7 steps
Depiction
Dead-End Product
Succinyl-carboxylic acid
C(CCC(=O)C(=O)O)(=O)C(O)=O
Depiction
Precursor
(1S,2S,4R,5S,7R)-4-methoxy-7-methyl-2-phenylmethoxy-6,8-dioxabicyclo[3.2.1]octane
C[C@@H]1[C@H]2[C@H](C[C@H]([C@@H](O1)O2)OC)OCC3=CC=CC=C3
12 steps
Depiction
Dead-End Product
1,2,4-Butantriol Alkohol
C(CC(C(O)O)O)O
Depiction
Precursor
(1S,2S,4R,5S,7R)-4-methoxy-7-methyl-2-phenylmethoxy-6,8-dioxabicyclo[3.2.1]octane
C[C@@H]1[C@H]2[C@H](C[C@H]([C@@H](O1)O2)OC)OCC3=CC=CC=C3
8 steps
Depiction
Dead-End Product
Rhodizonic acid
c1(c(c(=O)c(c(c1=O)O)O)=O)=O
Depiction
Upstream Precursor
(1R,2S,4R,5R,7S)-7-(chloromethyl)-2-[(2-chlorophenyl)methoxy]-4-methoxy-6,8-dioxabicyclo[3.2.1]octane
CO[C@@H]1C[C@@H]([C@@H]2[C@H](O[C@H]1O2)CCl)OCC3=CC=CC=C3Cl
Abiotic
Depiction
Product
(1S,2S,4R,5S,7R)-4-methoxy-7-methyl-2-phenylmethoxy-6,8-dioxabicyclo[3.2.1]octane
C[C@@H]1[C@H]2[C@H](C[C@H]([C@@H](O1)O2)OC)OCC3=CC=CC=C3
Depiction
Upstream Precursor
(1R,2S,4R,5R,7S)-7-(chloromethyl)-2-[(2-chlorophenyl)methoxy]-4-methoxy-6,8-dioxabicyclo[3.2.1]octane
CO[C@@H]1C[C@@H]([C@@H]2[C@H](O[C@H]1O2)CCl)OCC3=CC=CC=C3Cl
Environmental
Depiction
Product
(1S,2S,4R,5S,7R)-4-methoxy-7-methyl-2-phenylmethoxy-6,8-dioxabicyclo[3.2.1]octane
C[C@@H]1[C@H]2[C@H](C[C@H]([C@@H](O1)O2)OC)OCC3=CC=CC=C3
Depiction
Upstream Precursor
COC1CC(C2C(OC1O2)CCl)OCC3=CC=CC=C3
Environmental
Depiction
Product
(1S,2S,4R,5S,7R)-4-methoxy-7-methyl-2-phenylmethoxy-6,8-dioxabicyclo[3.2.1]octane
C[C@@H]1[C@H]2[C@H](C[C@H]([C@@H](O1)O2)OC)OCC3=CC=CC=C3
Depiction
Upstream Precursor
COC1CC(C2C(OC1O2)C)OCC3=CC=CC=C3Cl
Environmental
Depiction
Product
(1S,2S,4R,5S,7R)-4-methoxy-7-methyl-2-phenylmethoxy-6,8-dioxabicyclo[3.2.1]octane
C[C@@H]1[C@H]2[C@H](C[C@H]([C@@H](O1)O2)OC)OCC3=CC=CC=C3
Depiction
Precursor
(1S,2S,4R,5S,7R)-4-methoxy-7-methyl-2-phenylmethoxy-6,8-dioxabicyclo[3.2.1]octane
C[C@@H]1[C@H]2[C@H](C[C@H]([C@@H](O1)O2)OC)OCC3=CC=CC=C3
Environmental
Depiction
Downstream Successor
4-Hydroxybenzyl Alcohol
OCC1=CC=C(C=C1)O
Depiction
Precursor
(1S,2S,4R,5S,7R)-4-methoxy-7-methyl-2-phenylmethoxy-6,8-dioxabicyclo[3.2.1]octane
C[C@@H]1[C@H]2[C@H](C[C@H]([C@@H](O1)O2)OC)OCC3=CC=CC=C3
Environmental
Depiction
Downstream Successor
4-Oxocyclohexa-2,5-diene-1-carbaldehyde
C1(C=CC(C=O)C=C1)=O
Depiction
Precursor
(1S,2S,4R,5S,7R)-4-methoxy-7-methyl-2-phenylmethoxy-6,8-dioxabicyclo[3.2.1]octane
C[C@@H]1[C@H]2[C@H](C[C@H]([C@@H](O1)O2)OC)OCC3=CC=CC=C3
Environmental
Depiction
Downstream Successor
3,4-Dihydroxybenzyl Alcohol
OCc1cc(c(cc1)O)O
No Original Precursors

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