Synthesis of chiral sulfoximines derived from 3-aminoquinazolinones and their catalysis of enantioselective diethylzinc addition to aldehydes

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Royal Soc Chemistry

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info:eu-repo/semantics/closedAccess

Özet

A series of sulfoxides were sulfoximinated using oxidative addition of 3-aminoquinazolinones by lead tetraacetate in the presence of hexamethyldisilazane. They were applied for the first time in catalytic enantioselective addition to aromatic aldehydes with a product enantiopurity (ee) of 92% in the case of 2-methoxybenzaldehyde.

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Controlled Diastereoselective Aziridination, Transition-State Geometry, Asymmetric-Synthesis, C-1-Symmetric Aminosulfoximines, Buthionine Sulfoximine, Styrene Derivatives, Ligands, Alkenes, Benzothiazines, 3-Acetoxyaminoquinazolinones

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Organic & Biomolecular Chemistry

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9

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22

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Onay

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