Towards the total synthesis of tangutorine by intramolecular Diels–Alder reaction

Wilkinson, JA; Ardes-Guisot, N; Ducki, S; Leonard, J

Abstract

The syntheses of 3,5-disubstituted-2-sulfolenes, and their participation in Pictet-Spengler reactions to give precursors of tangutorine, are described.

Citation

Wilkinson, J., Ardes-Guisot, N., Ducki, S., & Leonard, J. (2005). Towards the total synthesis of tangutorine by intramolecular Diels–Alder reaction. Tetrahedron Letters, 46(46), 8053-8056. https://doi.org/10.1016/j.tetlet.2005.09.058

• Journal Article Type: Article
• Publication Date: Nov 14, 2005
• Deposit Date: Aug 8, 2007
• Journal: Tetrahedron Letters
• Print ISSN: 0040-4039
• Publisher: Elsevier
• Peer Reviewed: Peer Reviewed
• Volume: 46
• Issue: 46
• Pages: 8053-8056
• DOI: https://doi.org/10.1016/j.tetlet.2005.09.058
• Keywords: Tangutorine, intramolecular diels–alder, sulfolene, tetrahydrothiophene, xanthate radical transfer
• Publisher URL: http://dx.doi.org/10.1016/j.tetlet.2005.09.058