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The birch reduction of heterocyclic compounds. III. Birch reduction-elimination reaction of 2- and 3-furancarboxylic acid derivatives

✍ Scribed by Yasuo Ohta; Man Onoshima; Masumi Tamura; Rika Tanaka; Yoshiki Morimoto; Takamasa Kinoshita; Kazuo Yoshihara

Publisher
Journal of Heterocyclic Chemistry
Year
1998
Tongue
English
Weight
314 KB
Volume
35
Category
Article
ISSN
0022-152X

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✦ Synopsis

Abstract

The Birch reduction of 2‐(1‐alkoxyalkyl)furan‐3‐carboxylic acids 1a‐f gave 2‐alkyl‐3‐furancarboxylic acids 2a‐f with loss of the alkoxyl group in excellent isolated yields.

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The birch reduction of heterocyclic comp
The birch reduction of heterocyclic compounds V Birch reduction of 2- and 5-acylfuran-3-carboxylic acids and reductive elimination of 2-(arylmethoxymethyl)furan-3-carboxylic acids
✍ Yasuo Ohta; Matsumi Doe; Yoshiki Morimoto; Takamasa Kinoshita 📂 Article 📅 2000 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 283 KB

## Abstract The Birch reduction of 2‐ and 5‐acylfuran‐3‐carboxylic acid **1** and **4** gave 2‐acyl‐2,3‐dihydrofuran‐3‐carboxylic acid **2** and 5‐acyltetrahydrofuran‐3‐carboxylic acid **5**, respectively. Further examination of the reductive elimination was also studied on 2‐(arylmethoxymethyl)fur

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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v