Remote control of Diels-Alder additions. Enantioselective synthesis of (2R)-1,2,3,4-tetrahydro-2-hydroxy-5,8-dimethoxynaphthalen-2-yl methyl ketone (Wong's anthracycline intermediate) from furfural-Reference-Cited by-同舟云学术

Remote control of Diels-Alder additions. Enantioselective synthesis of (2R)-1,2,3,4-tetrahydro-2-hydroxy-5,8-dimethoxynaphthalen-2-yl methyl ketone (Wong's anthracycline intermediate) from furfural

Published:1997-10 Issue:20 Volume:8 Page:3497-3501
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Theurillat-Moritz Viviane,Guidi Antonio,Vogel Pierre

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference35 articles.

1. Diels-alder stereo- and regioselectivity controlled by remote substituents and solvent. Cycloadditions of 1-(dimethoxymethyl)-2,3-bis(methylene)-7-oxabicyclo[2.2.1]Heptane

2. Diels-AlderRegioselectivity Controlled by Remote Substituents. The Cycloadditions of 1-(Dimethoxymethyl)-2,3-dimethylidene- and -2,3,5,6-tetramethylidene-7-oxabicyclo[2.2.1]heptanes

3. New chiral auxiliaries and new optically pure ketene equivalents derived from tartaric acids. Improved synthesis of (−)-7-oxabicyclo[2.2.1]hept-5-en-2-one.

4. Asymmetric Synthesis and DNA Intercalation of (−)-6-[[(Aminoalkyl)oxy]methyl]-4-demethoxy-6,7- dideoxydaunomycinones1,

5. Enantiomerically pure Diels-Alder adducts of maleic anhydride to furfural acetals through thermodynamic control. Single crystal and molecular structure of (1S,4R,4′S,5′S)-1-(4′,5′-dimethyldioxolan-2′-yl)-5,6-dimethylidene-7-oxabicyclo[2.2.1]hept-2-ene

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