Expeditious novel routes to enantiopure 3-amino tetrahydrofuran hydrochloride

R Ramanujam, S Ganjihal, N Kalyanam…

Index: Ramanujam, Rajendran; Ganjihal, Savita; Kalyanam, Nagabushanam; Majeed, Muhammed Tetrahedron Asymmetry, 2013 , vol. 24, # 11 p. 663 - 668

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Citation Number: 4

Abstract

The synthesis of chemically and enantiomerically pure (S)-3-amino tetrahydrofuran hydrochloride starting from the natural amino acids, l-aspartic acid or l-methionine is described. The process involves no chromatography and can be easily carried out on a large scale. The enantiopurity of the final product was established by NMR and chiral HPLC methods.