Diastereoselective Synthesis of β‐Nitro‐ and β‐Aminoalcohols
1981; Wiley; Volume: 20; Issue: 4 Linguagem: Inglês
10.1002/anie.198103971
ISSN1521-3773
AutoresDieter Seebàch, Albert K. Beck, Friedrich Lehr, Thomas Weller, Ernest W. Colvin,
Tópico(s)Chemical Synthesis and Analysis
ResumoAlmost pure diastereoisomers of β-amino alcohols, important as synthons, can be prepared via the O-silylated nitroalcohols (1). Compounds (1) are accessible by protonation of the corresponding lithium salts or by addition of silylated aci-nitro derivatives R2CH = NO2Si tBuMe2 to aldehydes R1CHO.
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