Organic & Biomolecular Chemistry 2010-06-21

A new synthesis of amino acid-based enantiomerically pure substituted 2,3,4,4a,5,6-hexahydro-1H-pyrazino[1,2-a]quinoxalines.

Krishnananda Samanta, Gautam Panda

Index: Org. Biomol. Chem. 8(12) , 2823-8, (2010)

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Abstract

A new series of enantiomerically pure 2,3,4,4a,5,6-hexahydro-1H-pyrazino[1,2-a]quinoxalines were synthesized for the first time in twelve steps from 1-fluoro-2-nitrobenzene and S-amino acids with 13-20% overall yields. First use of intramolecular Mitsunobu cyclization for 1,2,3,4-tetrahydroquinoxalines followed by PPh(3)/I(2)/imidazole mediated 6-exo-tet cyclization were the key steps.

Related Compounds

  • 1-Fluoro-2-nitrobe...

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