Hello guys! I'm trying to understand the applications of chemical reactions using RDKit and the SMARTS concepts. I am testing, as an example, oxidation of aromatic rings:
rxn = AllChem.ReactionFromSmarts( '[#6:1]-[#8:2]-[c:3]1ccccc1>>[#8:2]-[c:3]1-cc-cc-c1') If I understand correctly, the above reaction is limited to always using benzene as a reagent. When I use naphthalene or anthracene as a reagent, the product is always simple phenol. How do I make the reaction more general? Thanks for any help! Best regards Fernando
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