Stereospecific total synthesis of (5.6)-dihete isomers

Claude Kugel, Jean Paul Lellouche, Jean Pierre Beaucourt, Gilles Niel, Jean Pierre Girard, Jean Claude Rossi

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

The first highly practical stereocontrolled synthesis of the four diastereoisomeric (5,6)-DiHETEs is described using the acetonides of D-and L-glyceraldehyde as a source of chirality. Their spectral and physico-chemical properties are also described.

Original languageEnglish
Pages (from-to)4947-4950
Number of pages4
JournalTetrahedron Letters
Volume30
Issue number37
DOIs
StatePublished - 1989
Externally publishedYes

Fingerprint

Dive into the research topics of 'Stereospecific total synthesis of (5.6)-dihete isomers'. Together they form a unique fingerprint.

Cite this