A facile procedure for the one-pot synthesis of unsymmetrical 2,5-disubstituted 1,3,4-oxadiazoles

Dabiri M; Salehi P; Baghbanzadeh M

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A facile procedure for the one-pot synthesis of unsymmetrical 2,5-disubstituted 1,3,4-oxadiazoles

机译：单锅合成不对称2,5-二取代1,3,4-恶二唑的简便方法

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摘要

Unsymmetrically 2,5-disubstituted 1,3,4-oxadiazoles were efficiently synthesized from the cyclization-oxidation reaction of acyl hydrazones. Also, the synthesis of the title compounds was achieved by the condensation of acyl hydrazides and aromatic aldehydes in the presence of ceric ammonium nitrate in dichloromethane. (c) 2006 Published by Elsevier Ltd.

机译：从酰基的环化-氧化反应有效地合成了不对称的2,5-二取代的1,3,4-恶二唑。同样，标题化合物的合成是通过在硝酸铈铵中在二氯甲烷中酰肼与芳族醛缩合而实现的。（c）2006年由Elsevier Ltd.发布。

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《Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry 》 |2006年第39期| 共4页
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Dabiri M; Salehi P; Baghbanzadeh M;
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正文语种 eng
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heterocycles; 1; 3; 4-oxadiazole; ceric ammonium nitrate; cyclization-oxidation; CARBOXYLIC-ACID HYDRAZIDES; SUPPORTED BURGESS REAGENT; MICROWAVE IRRADIATION; REUSABLE CATALYST; N-ACYLHYDRAZONES; EFFICIENT; DERIVATIVES; CYCLIZATION; OXIDATION; WATER;

机译：杂环;1;3;4-二唑;

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1. A facile procedure for the one-pot synthesis of unsymmetrical 2,5-disubstituted 1,3,4-oxadiazoles [J] . Dabiri M, Salehi P, Baghbanzadeh M Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry . 2006 ,第39期

机译：单锅合成不对称2,5-二取代1,3,4-恶二唑的简便方法
2. Trichloroisocyanuric Acid–Mediated One-Pot Synthesis of Unsymmetrical 2,5-Disubstituted 1,3,4-Oxadiazoles at Ambient Temperature [J] . D. M. Pore, S. M. Mahadik, U. V. Desai Synthetic Communications . 2008 ,第16a18期

机译：三氯异氰尿酸在环境温度下通过一锅法合成不对称的2,5-二取代的1,3,4-恶二唑
3. An expeditious and one-pot synthesis of unsymmetrical 2,5-disubstituted-1,3,4-oxadiazoles under microwave irradiation and solvent-free conditions [J] . Nasser Montazeri, Kurosh Rad-Moghadam 中国化学快报（英文版） . 2008 ,第010期

机译：在微波辐射和无溶剂条件下快速，一锅法合成不对称2,5-二取代-1,3,4-恶二唑
4. An Efficient Approach to Synthesis of 2,5-Disubstituted-l, 3, 4-oxadiazole Containing Furan Using Microwave Irradiation [C] . Cui Zining, Zhou Xinyu, Li Ying, International Symposium on Pesticide and Environmental Safety . 2007

机译：使用微波辐射合成含有呋喃的2,5-二取代-1,3,4-恶二唑的有效方法
5. Part I: Extension of 1,3,4-oxadiazole chemistry: Studies toward the total synthesis of aspidospermidine. Part II: Progress toward the total synthesis of rebeccamycin [D] . Tao, Houchao 2007

机译：第一部分：1,3,4-恶二唑化学反应的扩展：研究了aspsperspermidine的总合成。第二部分：瑞贝卡霉素全合成的进展
6. Facile solid phase peptide synthesis with a Re-lysine conjugate generated via a one-pot procedure [O] . Kullapa Chanawanno, Joel Caporoso, Vinay Kondeti, -1

机译：通过一锅法生成带有Re-赖氨酸共轭物的简便固相肽合成
7. A facile one-pot synthesis of novel 2,5-disubstituted-1,3,4-oxadiazoles under conventional and microwave conditions and evaluation of their in vitro antimicrobial activities [O] . Nida N. Farshori, Abdul Rauf, Maqsood A. Siddiqui, 2017

机译：在常规和微波条件下容易地一锅法合成新的2,5-二取代-1,3,4-恶二唑，并评价其体外抗菌活性

A facile procedure for the one-pot synthesis of unsymmetrical 2,5-disubstituted 1,3,4-oxadiazoles

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