Application of the asymmetric chelate-enolate Claisen rearrangement to the synthesis of 5-epi-isofagomine

DOI: 10.1016/S0040-4039(97)10855-3

Source and publish data:

Tetrahedron Letters p. 817 - 818 (1998)

Update date:2022-09-26

Topics:

Authors:

Kazmaier, Uli

Schneider, Christiane

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Article abstract of DOI:10.1016/S0040-4039(97)10855-3

Chelate-enolate Claisen rearrangement of a N-protected chiral amino acid ester gave rise to a γ,δ-unsaturated amino acid, which could be converted to the potential glycosidase inhibitor 5-epi-isofagomine (9) in a straightforward and a highly stereoselecti

Full text of DOI:10.1016/S0040-4039(97)10855-3

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