An efficient conversion of chiral α-amino acids to enantiomerically pure 3-amino cyclic amines

Article abstract of DOI:10.1080/00397919808004949

Enantiomerically pure 3-amino cyclic amines such as 3-amino pyrrolidine, 3-amino piperidine, and 2,3,4,5,6,7-hexahydro-1H-azepine have been synthesized in high yields from the optically active natural α-amino acids such as L-aspartic acid, L-glutamic acid, L-2-aminoadipic acid, and their enantiomers.

Full text of DOI:10.1080/00397919808004949

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An Efficient Conversion of
Chiral α-Amino Acids to
Enantiomerically Pure 3-
Amino Cyclic Amines
Sung-Hwan Moon a & Sujin Lee a
a Central Research Laboratory, ChoongWae
Pharma Corporation , 146–141 Annyungri
Taeaneup, Hwasungkun, Kyungkido, 445 - 970,
Republic of Korea E-mail:
Published online: 16 Aug 2006.
To cite this article: Sung-Hwan Moon & Sujin Lee (1998) An Efficient Conversion
of Chiral α-Amino Acids to Enantiomerically Pure 3-Amino Cyclic Amines,
Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 28:21, 3919-3926, DOI: 10.1080/00397919808004949
To link to this article: http://dx.doi.org/10.1080/00397919808004949
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