A four-step total synthesis of radermachol

M. Buccini, Matthew Piggott

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

Radermachol has been synthesized in four steps and an overall yield of 22% via key ytterbium triflate catalyzed furannulation and intramolecular nucleophilic acylation reactions. © 2014 American Chemical Society.
Original languageEnglish
Pages (from-to)2490-2493
JournalOrganic Letters
Volume16
Issue number9
DOIs
Publication statusPublished - 2014

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Ytterbium
acylation
Acylation
ytterbium
synthesis
radermachol

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Buccini, M. ; Piggott, Matthew. / A four-step total synthesis of radermachol. In: Organic Letters. 2014 ; Vol. 16, No. 9. pp. 2490-2493.
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A four-step total synthesis of radermachol. / Buccini, M.; Piggott, Matthew.

In: Organic Letters, Vol. 16, No. 9, 2014, p. 2490-2493.

Research output: Contribution to journalArticle

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T1 - A four-step total synthesis of radermachol

AU - Buccini, M.

AU - Piggott, Matthew

PY - 2014

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JO - Organic Letters

JF - Organic Letters

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