Synthesis of tert-Alkyl Amino Hydroxy Carboxylic Esters via an Intermolecular Ene-Type Reaction of Oxazolones and Enol Ethers
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tert-Alkyl amino hydroxy carboxylic acids are abundantly present within the structure of many biologically active natural products. We describeherein the synthesis of these substrates using an oxazolone-mediated ene-type reaction with enol ethers followed by NaBH4 reduction of theintermediate oxazolone.

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