Towards the total synthesis of ambruticin: Preparation of the fully functionalised right-hand portion using the intramolecular silyl-modified Sakurai (ISMS) annulation

Marko, Istvan;Bayston, DJ.
(1996) Synthesis : journal of synthetic organic chemistry — n° 2, p. 297-& (1996)

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  • Marko, IstvanUCLouvain
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  • Bayston, DJ.
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Abstract
The concise synthesis of the fully functionalised right-hand dihydropyran subunit of the antifungal antibiotic ambruticin (1), using the ISMS annulation as the key-step, is described.
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Marko, I., & Bayston, DJ. (1996). Towards the total synthesis of ambruticin: Preparation of the fully functionalised right-hand portion using the intramolecular silyl-modified Sakurai (ISMS) annulation. Synthesis : journal of synthetic organic chemistry, 2, 297-&. https://doi.org/10.1055/s-1996-4185 (Original work published 1996)