A new method for generation of non-stabilized α-amino-substituted carbanions by the reaction of magnesium carbenoids with N-lithio arylamines: their reactivity and a new synthesis of α-amino acid derivatives
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference57 articles.
1. Reviews concerning the stabilized α-amino-substituted carbanions:
2. Metalation and electrophilic substitution of amine derivatives adjacent to nitrogen: .alpha.-metallo amine synthetic equivalents
3. Some recent papers concerning generation and chemistry of stabilized α-amino-substituted carbanions:
4. Lithiation of N-boc-2-methyltetrahydro-1,3-oxazine: a synthetic equivalent for 1-lithio-3-hydroxy-1-propylamine
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1. Use of (Cyclopentadienone)iron Tricarbonyl Complexes for C–N Bond Formation Reactions between Amines and Alcohols;The Journal of Organic Chemistry;2017-09-28
2. Recent Advances in Magnesium Carbenoid Chemistry;Synthesis;2017-09-12
3. Synthesis of small ring-containing conjugated dienes via the coupling reaction of cyclopropyl- and cyclobutylmagnesium carbenoids with α-sulfonylallyllithiums;Tetrahedron;2013-05
4. New Synthetic Methods by Using the Electrophilic Nature of Magnesium Carbenoids: Recent Progress and Elucidation of the Essence of the Reactivity by DFT Calculation;Journal of Synthetic Organic Chemistry, Japan;2013
5. Quantum chemical characterization of magnesium carbenoids;Journal of Organometallic Chemistry;2012-09
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