Synthesis of the cytostatic cyclic tetrapeptide, chlamydocin

DOI: 10.1016/S0040-4039(00)87854-5

Source and publish data:

Tetrahedron Letters p. 5305 - 5308 (1983)

Update date:2022-07-31

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Authors:

Rich Rich

Gardner Gardner

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Article abstract of DOI:10.1016/S0040-4039(00)87854-5

Chlamydocin has been synthesized by a route utilizing allylic hydroxylation and epoxidation of the DL-2-amino-9-decenoic acid residue to form the 2-amino-8-oxo-9,10-epoxydecanoic acid residue.

Full text of DOI:10.1016/S0040-4039(00)87854-5

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