A general method for the synthesis of C-glycosyl amino acids is described here. The stereoisomerically pure tyrosine analigues alpha-L-4 and beta-L-6 are prepared in reasonable overall yields from all l derivatives 10 and 11. The key step is a benzannulation procedure which is employed in the creation of the aromatic ring that bears the amino acid function.

A Novel General Route for the Synthesis of C-Glycosyl Tyrosine Analogues.

SERRA STEFANO;
2002

Abstract

A general method for the synthesis of C-glycosyl amino acids is described here. The stereoisomerically pure tyrosine analigues alpha-L-4 and beta-L-6 are prepared in reasonable overall yields from all l derivatives 10 and 11. The key step is a benzannulation procedure which is employed in the creation of the aromatic ring that bears the amino acid function.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/199498
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