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

Access to Document

10.3987/com-03-s(p)71

Cite this

@article{588e8144f3684e70bfe722d4ad694784,

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.}",

year = "2004",

month = jan,

day = "1",

doi = "10.3987/com-03-s(p)71",

language = "English",

volume = "62",

pages = "713--734",

journal = "Heterocycles",

issn = "0385-5414",

publisher = "Japan Institute of Heterocyclic Chemistry",

}

TY - JOUR

T1 - Stereoselective total synthesis of the nonenolide (+)-microcarpalide

AU - Banwell, Martin G.

AU - Loong, David T.J.

PY - 2004/1/1

Y1 - 2004/1/1

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 - http://www.scopus.com/inward/record.url?scp=0347090287&partnerID=8YFLogxK

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

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

M3 - Article

SN - 0385-5414

VL - 62

SP - 713

EP - 734

JO - Heterocycles

JF - Heterocycles

ER -

Stereoselective total synthesis of the nonenolide (+)-microcarpalide

Abstract

Access to Document

Other files and links

Fingerprint

Cite this