The role of substituents in retro Diels–Alder extrusion of CO2 from 2(H)-pyrone cycloadducts-Reference-Cited by-同舟云学术

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The role of substituents in retro Diels–Alder extrusion of CO2 from 2(H)-pyrone cycloadducts

Published:2016-10 Issue:40 Volume:72 Page:6021-6024
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Abdullahi Mohamed Haji,Thompson Lee M.,Bearpark Michael J.,Vinader Victoria,Afarinkia Kamyar

Funder

Engineering and Physical Sciences Research Council

Yorkshire Cancer Research

Yorkshire Enterprise Fellowships

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference41 articles.

1. Diels-Alder cycloadditions of 2-pyrones and 2-pyridones

2. Recent advances in diels-alder cycloadditions of 2-pyrones

3. Natural and synthetic 2H-pyran-2-ones and their versatility in organic synthesis

4. A convenient synthesis of isotopically labelled anthraquinones, chrysophanol, islandicin, and emodin. Incorporation of [methyl-2H3]chrysophanol into tajixanthone in Aspergillus variecolor

5. First Inverse Electron-Demand Diels–Alder Methodology of 3-Chloroindoles and Methyl Coumalate to Carbazoles

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