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Stereoselective double ring closing metathesis reactions in the synthesis of spirocyclic compounds

✍ Scribed by Debra J Wallace; Cameron J Cowden; Derek J Kennedy; Michael S Ashwood; Ian F Cottrell; Ulf-H Dolling

Book ID: 104210003
Publisher: Elsevier Science
Year: 2000
Tongue: French
Weight: 91 KB
Volume: 41
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)00095-2

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✦ Synopsis

The first diastereoselective double ring closing metathesis reaction to afford a spirocyclic compound is reported. Cyclisation of amino acid derived tetraenes 7 selectively afforded spirocyclic compounds 8.

📜 SIMILAR VOLUMES

ChemInform Abstract: Stereoselective Dou

ChemInform Abstract: Stereoselective Double Ring Closing Metathesis Reactions in the Synthesis of Spirocyclic Compounds.

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ChemInform Abstract: Stereoselective Dou

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A quadruple ring-closing metathesis reaction in the synthesis of bis-spirocyclic compounds: extending the scope of metathesis chemistry

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The first example of a quadruple ring-closing metathesis reaction is reported. The reaction of the C2 symmetric octaene 3 afforded bis-spirocyclic compounds in high yield.

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✍ Debra J. Wallace 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 16 KB 👁 1 views

The synthesis of angularly fused tricycl

The synthesis of angularly fused tricyclic compounds via tandem ring closing metathesis reactions

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Application of Ring-Closing Metathesis R

Application of Ring-Closing Metathesis Reactions in the Synthesis of Epothilones

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