The synthesis and chemistry of functionalized furochromones.4.1 Addition of nitronate anions to 30bromochromone and 6-bromofurochromone. An expedient route to furo(3′,2′:6,7)-benzopyrano(2,3-d)-isoxazolones and chromono(2,3-d)isoxazolones.-Reference-Cited by-同舟云学术

The synthesis and chemistry of functionalized furochromones.4.1 Addition of nitronate anions to 30bromochromone and 6-bromofurochromone. An expedient route to furo(3′,2′:6,7)-benzopyrano(2,3-d)-isoxazolones and chromono(2,3-d)isoxazolones.

Published:1992-02 Issue:8 Volume:33 Page:993-996
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Gammill Ronald B.,Nash Sharon A.,Bell Larry T.,Watt William

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference17 articles.

1. Khellin analogs. 1. General topological requirements for lipid-altering activity in furochromones

2. Antiatherosclerotic agents. A structurally novel bivalent inhibitor of AcylCoA:cholesterol O-acyltransferase with systemic activity

3. The synthesis and chemistry of functionalized furochromones. 2. The synthesis, Sommelet-Hauser rearrangement, and conversion of 4,9-dimethoxy-7-[(methylthio)methyl]-5H-furo(3,2-g)benzopyran-5-one to ammiol

4. The addition of amines to 3-bromochromone and 6-bromofurochromone. An unexpected ring contraction of the pyrone ring.

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