A concise total synthesis of (±)-anthecularin

Yi Li; Christopher C. Nawrat; Gerald Pattenden; Johan M. Winne

doi:10.1039/b819454h

A concise total synthesis of (±)-anthecularin

Yi Li^*, Christopher C. Nawrat, Gerald Pattenden, Johan M. Winne

^*Corresponding author for this work

University of Nottingham

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

27 Citations (Scopus)

Abstract

A total synthesis of the novel sesquiterpene anthecularin 1, isolated from Greek Anthemis auriculata, based on an intramolecular [5+2] (1,3-dipolar) cycloaddition involving the oxidopyrylium ion 12 derived from the furanmethanol 9, is described.

Original language	English
Pages (from-to)	639-640
Number of pages	2
Journal	Organic and Biomolecular Chemistry
Volume	7
Issue number	4
DOIs	https://doi.org/10.1039/b819454h
Publication status	Published - 2009
Externally published	Yes

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10.1039/b819454h

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title = "A concise total synthesis of (±)-anthecularin",

abstract = "A total synthesis of the novel sesquiterpene anthecularin 1, isolated from Greek Anthemis auriculata, based on an intramolecular [5+2] (1,3-dipolar) cycloaddition involving the oxidopyrylium ion 12 derived from the furanmethanol 9, is described.",

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AU - Li, Yi

AU - Nawrat, Christopher C.

AU - Pattenden, Gerald

AU - Winne, Johan M.

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AB - A total synthesis of the novel sesquiterpene anthecularin 1, isolated from Greek Anthemis auriculata, based on an intramolecular [5+2] (1,3-dipolar) cycloaddition involving the oxidopyrylium ion 12 derived from the furanmethanol 9, is described.

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U2 - 10.1039/b819454h

DO - 10.1039/b819454h

M3 - Article

C2 - 19194574

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SN - 1477-0520

VL - 7

SP - 639

EP - 640

JO - Organic and Biomolecular Chemistry

JF - Organic and Biomolecular Chemistry

IS - 4

ER -

A concise total synthesis of (±)-anthecularin

Abstract

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