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Stereoselective synthesis of the tetrasubstituted cyclohexane core of a monocyclic mevinic acid analogue

โœ Scribed by Mikhail S. Ermolenko; Alain Olesker; Gabor Lukacs

Publisher
Elsevier Science
Year
1994
Tongue
French
Weight
288 KB
Volume
35
Category
Article
ISSN
0040-4039

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โœฆ Synopsis

Stereoselective synthesis of a 1,2,3,4-tetrasubstituted cyclohexane 23, intermediate towards Karanewsky's monocyclic Compactin analogue 3, has been performed starting from levoglucosan 4.

๐Ÿ“œ SIMILAR VOLUMES

A new strategy for the synthesis of mevi
A new strategy for the synthesis of mevinic acid analogues
โœ Pascal Boquel; Yves Chapleur ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 170 KB

The reaction of the allylic carbonate 2 with organocopper derivatives is the key step of a new strategy for the synthesis of mevinic acid analogues.