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Method for diastereoselective preparation of piperidines functionalised in positions 2 and 4 for use as synthesis intermediates
Method for diastereoselective preparation of piperidines functionalised in positions 2 and 4 for use as synthesis intermediates
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机译:用于在位置2和4上官能化的哌啶的非对映选择性制备方法,用作合成中间体
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摘要
The invention concerns a method for preparing, with diastereoselective induction, a piperidine monosubstituted in position 4 and functionalised in position 2, comprising steps which consist in: (i) reacting the corresponding N-protected piperidine, monosubstituted in position 4 and non-functionalised in position 2, with a strong base so as to form the negatively charged corresponding carbanion in position 2; then (ii) reacting said carbanion with an electrophilic reagent, with a volume less than 80 ANGSTROM 3 or more than 100 ANGSTROM 3.
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