Ruthenium-catalyzed ring closing olefin metathesis of non-natural α-amino acids

DOI: 10.1016/S0040-4039(96)02390-8

Source and publish data:

Tetrahedron Letters p. 677 - 680 (1997)

Update date:2022-08-05

Topics: Catalyzed Olefin Metathesis Ruthenium

Authors:

Rutjes, Floris P. J. T.

Schoemaker, Hans E.

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Article abstract of DOI:10.1016/S0040-4039(96)02390-8

The use of various enantiopure amino acid-derived diolefins as substrates for the ring closing olefin metathesis reaction (RCM) has been investigated. This reaction has been shown to be an efficient transformation for providing highly functionalized 6- and 7-membered ring amino acids.

Full text of DOI:10.1016/S0040-4039(96)02390-8

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