Facile synthesis of highly substituted 2-pyrone derivatives via a tandem Knoevenagel condensation/lactonization reaction of β-formyl-esters and 1,3-cyclohexadiones-Reference-Cited by-同舟云学术

Facile synthesis of highly substituted 2-pyrone derivatives via a tandem Knoevenagel condensation/lactonization reaction of β-formyl-esters and 1,3-cyclohexadiones

Published:2014-04 Issue:18 Volume:55 Page:2908-2911
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Moghaddam Firouz Matloubi,Mirjafary Zohreh,Javan Marjan Jebeli,Motamen Sara,Saeidian Hamid

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference38 articles.

1. 2-Pyrone natural products and mimetics: isolation, characterisation and biological activity

2. An efficient synthesis of 4-alkenyl/alkynyl-6-methyl-2-pyrones via Pd-catalysed coupling on 4-bromo-6-methyl-2-pyrone

3. Diels–Alder cycloaddition of 5-aryl-2-pyrones

4. One-Pot Stereoselective Synthesis of Tricyclic Bislactones from 2-Pyrones and 2-Methoxyfuran

5. 4-Alkoxy-6-alkyl-2-pyrones as Precursors for 4-Alkoxy-6-alkyl-2-aminobenzoic Acid Derivatives

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