This microreview covers recent advances in the use of ring‐closing metathesis for the synthesis of carbocycles from carbohydrates. Various strategies for the synthesis of α,ω‐dienes from carbohydrates are presented, which give rise to a large variety of dienes with different stereochemistries, protecting groups and substituents. Subsequent ring‐closing metathesis with a ruthenium carbene complex affords highly functionalized carbocycles with ring sizes ranging from five‐ to eight‐membered rings. The application of these methods for the synthesis of carbocyclic natural products from carbohydrates is also demonstrated.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)
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Robert Madsen (2006) studied this question.
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