Aluminium-mediated Reductive Dimerization of Aromatic Dialdehydes-Reference-Cited by-同舟云学术

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Aluminium-mediated Reductive Dimerization of Aromatic Dialdehydes

Published:1999-03 Issue:3 Volume:23 Page:210-211
ISSN:1747-5198
Container-title:Journal of Chemical Research
language:en
Short-container-title:Journal of Chemical Research

Author:

Sahade Daniel A.¹,Kawaji Takatoshi¹,Sawada Tsuyoshi²,Mataka Shuntaro²,Thiemann Thies²,Tsukinoki Takehito³,Tashiro Masashi³

Affiliation:

1. Department of Molecular Science and Technology, Graduate School of Engineering Sciences, Kyushu University, 6-1 Kasuga Koh-en, Kasuga-shi, Fukuoka 816-8580, Japan

2. Institute of Advanced Material Study, Kyushu University, 6-1 Kasuga Koh-en, Kasuga-shi, Fukuoka 816-8580, Japan

3. Central Institute for Science, Tohwa University, 1-1-1, Chikushigaoka, Minami-ku, Fukuoka 815-0036, Japan

Abstract

Pinacol coupling reaction of several aromatic dialdehydes 1a-d using inexpensive aluminum powder as a reductive reagent in aqueous NaOH-methanol media afforded dimeric compounds 2a-d as main products, in which only one carbonyl group of 1 was reduced.

Publisher

SAGE Publications

Subject

General Chemistry

Link

http://journals.sagepub.com/doi/pdf/10.1177/174751989902300320

Reference11 articles.

1. Some organic reactions promoted by samarium diiodide

2. A novel method for the preparation of perfluoroalkylmethyl substituted electrophilic cyclopropane derivatives

3. [2.2]Metacyclophanes having hydroxy groups on the bridge

4. An investigation of polymerization via reductive coupling of carbonyls

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