Utilization of a 1,2-Dioxine for the Synthesis of the Four Possible Stereoisomers of Oak Lactone-Reference-Cited by-同舟云学术

Utilization of a 1,2-Dioxine for the Synthesis of the Four Possible Stereoisomers of Oak Lactone

Published:2006-01-04 Issue:3 Volume:8 Page:463-466
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Brown Rachel C.¹,Taylor Dennis K.¹,Elsey Gordon M.¹

Affiliation:

1. The Australian Wine Research Institute, Glen Osmond, South Australia 5064, School of Chemistry, Physics and Earth Sciences, Flinders University, Adelaide, South Australia 5001, Department of Chemistry, University of Adelaide, South Australia 5005, and Cooperative Research Centre for Viticulture, PO Box 154, Glen Osmond, South Australia 5064, Australia

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol052754u

Reference24 articles.

1. Precursors to oak lactone. Part 2: Synthesis, separation and cleavage of several β-d-glucopyranosides of 3-methyl-4-hydroxyoctanoic acid

2. Synthesis of both enantiomers of .gamma.-substituted .alpha.,.beta.-unsaturated .gamma.-lactones

3. New entry to chiral butenolide synthons. Application to expeditious syntheses of (+)-nephrosteranic acid, (+)-trans-whisky lactone, and (+)-trans-cognac lactone

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