Stereoselective total synthesis of the nonenolide (+)-microcarpalide

Martin G. Banwell; David T.J. Loong

doi:10.3987/com-03-s(p)71

Stereoselective total synthesis of the nonenolide (+)-microcarpalide

Martin G. Banwell^*, David T.J. Loong

^*Corresponding author for this work

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

25 Citations (Scopus)

Abstract

The enantiomer [(+)-1] of the nonenolide natural product microcarpalide [(-)-1] has been prepared from (S)-malic acid (3) and 3-decyn-1-ol (11) via a sixteen step sequence involving, inter alia, two metathesis processes.

Original language	English
Pages (from-to)	713-734
Number of pages	22
Journal	Heterocycles
Volume	62
DOIs	https://doi.org/10.3987/com-03-s(p)71
Publication status	Published - 1 Jan 2004

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title = "Stereoselective total synthesis of the nonenolide (+)-microcarpalide",

abstract = "The enantiomer [(+)-1] of the nonenolide natural product microcarpalide [(-)-1] has been prepared from (S)-malic acid (3) and 3-decyn-1-ol (11) via a sixteen step sequence involving, inter alia, two metathesis processes.",

author = "Banwell, \{Martin G.\} and Loong, \{David T.J.\}",

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AU - Loong, David T.J.

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N2 - The enantiomer [(+)-1] of the nonenolide natural product microcarpalide [(-)-1] has been prepared from (S)-malic acid (3) and 3-decyn-1-ol (11) via a sixteen step sequence involving, inter alia, two metathesis processes.

AB - The enantiomer [(+)-1] of the nonenolide natural product microcarpalide [(-)-1] has been prepared from (S)-malic acid (3) and 3-decyn-1-ol (11) via a sixteen step sequence involving, inter alia, two metathesis processes.

UR - https://www.scopus.com/pages/publications/0347090287

U2 - 10.3987/com-03-s(p)71

DO - 10.3987/com-03-s(p)71

M3 - Article

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VL - 62

SP - 713

EP - 734

JO - Heterocycles

JF - Heterocycles

ER -

Stereoselective total synthesis of the nonenolide (+)-microcarpalide

Abstract

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