AN INVESTIGATION OF THE MITSUNOBU REACTION IN THE PREPARATION OF PEPTIDE OXAZOLINES, THIAZOLINES, AND AZIRIDINES

DOI: 10.1016/S0040-4039(00)60949-8

Source and publish data:

Tetrahedron Letters p. 6267 - 6270 (1992)

Update date:2022-07-30

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Authors:

Wipf, Peter

Miller, Chris P.

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Article abstract of DOI:10.1016/S0040-4039(00)60949-8

The diisopropyl azodicarboxylate-triphenylphosphine mediated cyclization of serine and allo-threonine derivatives provides peptide oxazolines, whereas cyclization of threonine containing substrates leads to N-acyl aziridines.In the thiopeptide series, onl

Full text of DOI:10.1016/S0040-4039(00)60949-8

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