A four-step total synthesis of radermachol

M. Buccini; Matthew Piggott

doi:10.1021/ol500862w

A four-step total synthesis of radermachol

M. Buccini, Matthew Piggott

Research output: Contribution to journal › Article › peer-review

29 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 language	English
Pages (from-to)	2490-2493
Journal	Organic Letters
Volume	16
Issue number	9
DOIs	https://doi.org/10.1021/ol500862w
Publication status	Published - 2014

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title = "A four-step total synthesis of radermachol",

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. {\textcopyright} 2014 American Chemical Society.",

author = "M. Buccini and Matthew Piggott",

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doi = "10.1021/ol500862w",

language = "English",

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journal = "Organic Letters",

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AU - Buccini, M.

AU - Piggott, Matthew

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U2 - 10.1021/ol500862w

DO - 10.1021/ol500862w

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JO - Organic Letters

JF - Organic Letters

SN - 1523-7052

IS - 9

ER -

A four-step total synthesis of radermachol

Abstract

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