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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

✍ Scribed by Yasuo Ohta; Matsumi Doe; Yoshiki Morimoto; Takamasa Kinoshita


Publisher
Journal of Heterocyclic Chemistry
Year
2000
Tongue
English
Weight
283 KB
Volume
37
Category
Article
ISSN
0022-152X

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✦ Synopsis


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)furan‐3‐carboxylic acids 7.


📜 SIMILAR VOLUMES


ChemInform Abstract: The Birch Reduction
✍ Yasuo Ohta; Matsumi Doe; Yoshiki Morimoto; Takamasa Kinoshita 📂 Article 📅 2001 🏛 John Wiley and Sons ⚖ 29 KB 👁 2 views

## 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

The birch reduction of heterocyclic comp
✍ Yasuo Ohta; Man Onoshima; Masumi Tamura; Rika Tanaka; Yoshiki Morimoto; Takamasa 📂 Article 📅 1998 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 314 KB

## 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.