Diels-Alder reactions of 6-alkyl-3,5-dichloro-2H-1,4-oxazin-2-ones with alkynes: Synthesis of 3,5-disubstituted 2,6-dichloropyridines

DOI: 10.1055/s-1991-26570

Source and publish data:

Synthesis p. 765 - 768 (1991)

Update date:2022-08-02

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Authors:

Meerpoel

Deroover

Van Aken

Lux Lux

Hoornaert

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Article abstract of DOI:10.1055/s-1991-26570

The Diels-Alder reactiion of 6-alkyl-3,5-dichloro-2H-1,4-oxazin-2-ones 1 with different types of acetylenic compounds 2 is shown to be a versatile method for the generation of variously substituted 2,6-dichloropyridines. In most cases a high degree of reg

Full text of DOI:10.1055/s-1991-26570

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Article Doi

Diels-Alder reactions of 6-alkyl-3,5-dichloro-2H-1,4-oxazin-2-ones with alkynes: Synthesis of 3,5-disubstituted 2,6-dichloropyridines

DOI: 10.1055/s-1991-26570

Source and publish data:

Authors:

Article abstract of DOI:10.1055/s-1991-26570

Full text of DOI:10.1055/s-1991-26570

Products guided by the article

R&D Labs maybe for 137521-01-8

Relevant to this article

On the Reaction of (Vinylimino)phosphoranes and Related Compounds. 20. Syntheses and Properties of Methanocyclodecapyridine Ring Systems

3-Hydroxyflavones vs. 3-hydroxyquinolinones: Structure-activity relationships and stability studies on RuII(arene) anticancer complexes with biologically active ligands

Enantioselective cyclopropanation of enals by oxidative N-heterocyclic carbene catalysis

Photochemical Cycloaddition of Phenanthrene-Fused Lactones to (E)-Anethole. Structural Effects and Dual Collapse Processes of an Exciplex Leading to Cycloadducts

Atom efficient preparation of zinc selenates for the synthesis of selenol esters under “On Water” conditions

Synthesis of the C1-C9 fragment of the potent antitumor agent dictyostatin

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