Control of theDiels-Alder-Addition Regioselectivity by Remote Olefins. Syntheses and Cycloadditions of 2,3,5-Trimethylidenebicyclo[2.2.1]heptane and 2,3,5,6,7-Pentamethylidenebicyclo[2.2.2]octane-Reference-Cited by-同舟云学术

Control of theDiels-Alder-Addition Regioselectivity by Remote Olefins. Syntheses and Cycloadditions of 2,3,5-Trimethylidenebicyclo[2.2.1]heptane and 2,3,5,6,7-Pentamethylidenebicyclo[2.2.2]octane

Published:1986-09-10 Issue:6 Volume:69 Page:1310-1322
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:de
Short-container-title:Helv. Chim. Acta

Author:

Burnier G�rald,Schwager Luis,Vogel Pierre

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Reference66 articles.

1. Control of the diels-alder addition regioselectivity by remote substituents. Synthesis of anthracycline precursors.

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. Synthesis andDiels-AlderReactivity of 1-(Dimethoxy)methyl-2,3,5,6-tetramethylidene-7-oxabicyclo[2.2.1]heptane. Preliminary communication

4. 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

5. Interactions between homoconjugated diene and epoxide functions. Effect on diels-alder regioselectivity

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