Efficient one-pot synthesis of enantiomerically pure N-protected-α-substituted piperazines from readily available α-amino acidsElectronic supplementary information (ESI) available. See DOI: 10.1039/c7nj04039c

A new pathway towards enantiomerically pure 3-substituted piperazines, bearing a benzyl protecting group, has been developed in good overall yields (83-92%), starting from commercially available N -protected amino acids. The methodology represents an efficient and simple one-pot procedure, employing...

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Hauptverfasser:	Jida, Mouhamad, Ballet, Steven
Format:	Artikel
Sprache:	eng
Online-Zugang:	Volltext
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