New Strategy for the Construction of Epoxy-Bridged Tetrahydropyran Frameworks from Trioxane Precursors: Application to a Concise Synthesis of a Riesling Acetal-Reference-Cited by-同舟云学术

New Strategy for the Construction of Epoxy-Bridged Tetrahydropyran Frameworks from Trioxane Precursors: Application to a Concise Synthesis of a Riesling Acetal

Published:2008-10-10 Issue:21 Volume:73 Page:8678-8681
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Riveira Martín J.¹,La-Venia Agustina¹,Mischne Mirta P.¹

Affiliation:

1. Instituto de Química Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas - Universidad Nacional de Rosario-CONICET, Suipacha 531, S2002LRK Rosario, Argentina

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo8017928

Reference27 articles.

1. Recent synthetic studies on the zaragozic acids (squalestatins)

2. Introduction of Bicyclic Ketal Chemistry: Synthesis and Transformation Reaction of 6,8-Dioxabicyclo[3.2.1]octane Skeletal System

3. Identification and synthesis of new bicyclic acetals from caddisflies (Trichoptera)

4. Enantioselective Synthesis of the Apple Aroma Constituent 1,3,3-Trimethyl-2,7-dioxabicyclo[2.2.1]heptane via Asymmetric Dihydroxylation

5. 3,4-Dihydroxy-7,8-dihydro-.beta.-ionone .beta.-D-glucopyranoside: natural precursor of 2,2,6,8-tetramethyl-7,11-dioxatricyclo[6.2.1.01,6]undec-4-ene (Riesling acetal) and 1,1,6-trimethyl-1,2-dihydronaphthalene in red currant (Ribes rubrum L.) leaves

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