Sonochemistry: A good, fast and clean method to promote the synthesis of 5-arylidene-2,4-thiazolidinediones

被引：16

作者：

Drawanz, Bruna B. ^{[1
]}

Ribeiro, Camila S. ^{[1
]}

Masteloto, Hellen G. ^{[1
]}

Neuenfeidt, Patricia D. ^{[1
,2
]}

Pereira, Claudio M. P. ^{[3
]}

Siqueira, Geonir. M. ^{[1
]}

Cunico, Wilson ^{[1
]}

机构：

[1] Univ Fed Pelotas UFPel, Lab Quim Aplicada Bioativos LaQuiABio, BR-96010900 Pelotas, RS, Brazil

[2] Univ Fed Santa Catarina, Lab Estrutura & Atividade LEAT, BR-88040970 Florianopolis, SC, Brazil

[3] Univ Fed Pelotas UFPel, Lab Heterociclos Bioat & Bioprospeccao, BR-96010900 Pelotas, RS, Brazil

来源：

ULTRASONICS SONOCHEMISTRY | 2014年 / 21卷 / 05期

关键词：

Thiazolidinediones; Sonochemistry; Aldol condensation; ULTRASOUND-ASSISTED SYNTHESIS; ARYLIDENE-THIAZOLIDINEDIONE; CONVENIENT SYNTHESIS; REDUCTASE; FACILE; 5-ARYLIDENETHIAZOLIDINE-2,4-DIONES;

D O I：

10.1016/j.ultsonch.2014.04.013

中图分类号：

O42 [声学];

学科分类号：

070206 ; 082403 ;

摘要：

The efficient synthesis of sixteen 5-arylidene-2,4-thiazolidinediones by aldol condensation reaction of 2,4-thiazolidinedione, mono- and di-substituted arenealdehydes and KOH using ultrasound irradiation is reported. The desired compounds were obtained in a few min (10-30 min) with moderate to good yields (25-81%). (C) 2014 Elsevier B.V. All rights reserved.

引用

页码：1615 / 1617

页数：3

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