An Efficient Stereocontrolled Strategy for the Synthesis of Hydroxyethylene Dipeptide Isosteres

DOI: 10.1021/jo00094a006

Source and publish data:

Journal of Organic Chemistry p. 4040 - 4041 (1994)

Update date:2022-08-11

Topics:

Authors:

Stuk, Timothy L.

Haight, Anthony R.

Scarpetti, David

Allen, Michael S.

Menzia, Jerome A.

et al. et al.

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Article abstract of DOI:10.1021/jo00094a006

A novel and practical synthesis of hydroxyethylene dipeptide isostere 9 from L-phenylalanine via the formation and stereospecific reduction of an enaminone is described.

Full text of DOI:10.1021/jo00094a006

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