The α:β ratio in the acetylation of furan and the “extended selectivity treatment” for electrophilic substitutions at the beta position of the furan ring-Reference-Cited by-同舟云学术

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The α:β ratio in the acetylation of furan and the “extended selectivity treatment” for electrophilic substitutions at the beta position of the furan ring

Published:1971-01 Issue:41 Volume:12 Page:3833-3836
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Ciranni Giovanna,Clementi Sergio

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference13 articles.

1. Solvolysis of furylmethylcarbinol derivatives

2. D.S. Noyce and H.J. Pavez, unpublished results.

3. S. Clementi and G. Marino, J. Chem. Soc. (B), in the press.

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1. Production ofp-Methylstyrene andp-Divinylbenzene from Furanic Compounds;ChemSusChem;2016-12-20

2. Electrophilic Substitution of Thiophene and its Derivatives;Chemistry of Heterocyclic Compounds: A Series Of Monographs;2008-01-02

3. A new method for the synthesis of silicon-and germanium-containing 2-acetylfurans and 2-acetylthiophenes;Chemistry of Heterocyclic Compounds;2007-02

4. Synthesis of polyfunctionalized furans from 3-acetyl-1-aryl-2-pentene-1,4-diones;Tetrahedron;2003-02

5. Furan;Encyclopedia of Reagents for Organic Synthesis;2001-04-15

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