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From galactose to highly functionalized seven- and eight-membered carbocyclic rings by ring-closing metathesis
1Laboratoire de Synthèse Organique associé au CNRS, Ecole Polytechnique, Palaiseau, France. hanna@poly.polytechnique.fr
Organic Letters
|September 16, 2000
Abstract:
[reaction: see text]A short synthesis of highly functionalized seven- and eight-membered carbocyclic rings from galactose derivatives has been achieved. The key steps are a zinc-mediated reductive ring opening of 6-iodogalactopyranoses and a subsequent ring-closing olefin metathesis using Grubbs' ruthenium catalyst.