Stereoselective hetero-Diels–Alder reaction of 3-(polyfluoroacyl)chromones with enol ethers. Novel synthesis of 2-RF-containing nicotinic acid derivatives-Reference-Cited by-同舟云学术

Stereoselective hetero-Diels–Alder reaction of 3-(polyfluoroacyl)chromones with enol ethers. Novel synthesis of 2-RF-containing nicotinic acid derivatives

Published:2008-10 Issue:44 Volume:64 Page:10172-10180
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Sosnovskikh Vyacheslav Ya.,Khalymbadzha Igor A.,Irgashev Roman A.,Slepukhin Pavel A.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference48 articles.

1. Heterodiene syntheses with .alpha.,.beta.-unsaturated carbonyl compounds

2. Hetero-diels-alder reactions of α-methoxymethylene substituted 1.3-dicarbonyl compounds with enol and enediol ethers

3. Diastereospecific synthesis of 2.6-dideoxy- and 2.4.6-trideoxy-sugars via hetero-diels-alder-reaction

4. Hetero-diels-alder reaction of enaminecarbaldehydes an entry to branched aminosugars

5. Reactivity of 2-methylene-1,3-dicarbonyl compounds. Inverse electron-demand Diels–Alder reactions with alkyl vinyl ethers

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