10-Camphorsulfonic acid ((+/-)-CSA) catalyzed facile one-pot synthesis of a new class of 2,5-disubstituted 1,3,4-oxadiazoles

Mule Siva Nagi Reddy; Battula Sailaja Kumari; Velupula Ganapathi; Guda Dinneswara Reddy; Bollikolla Hari Babu

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10-Camphorsulfonic acid ((+/-)-CSA) catalyzed facile one-pot synthesis of a new class of 2,5-disubstituted 1,3,4-oxadiazoles

机译：10-樟脑磺酸（（+/-）-CSA）催化一锅合成新型的2,5-二取代1,3,4-恶二唑

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摘要

A convenient and efficient one-pot synthesis of 2,5-disubstituted-1,3,4-oxadizoles is described. Various carboxylic acid hydrazides reacted efficiently with different carboxylic acid chlorides and 10-camphorsulfonic acid. This methodology was successfully applied to the synthesis of a series of 2H-chromene substituted 1,3,4-oxadiazole derivatives in good to high yields.

机译：描述了一种方便且有效的一锅合成2,5-二取代-1,3,4-恶二唑。各种羧酸酰肼可与不同的羧酸氯化物和10-樟脑磺酸有效地反应。该方法成功地应用于高产率到高产率的一系列2H-亚甲基取代的1,3,4-恶二唑衍生物的合成。

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《RSC Advances》 |2014年第102期|共7页
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Mule Siva Nagi Reddy; Battula Sailaja Kumari; Velupula Ganapathi; Guda Dinneswara Reddy; Bollikolla Hari Babu;
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中图分类化学;
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1. 10-Camphorsulfonic acid ((+/-)-CSA) catalyzed facile one-pot synthesis of a new class of 2,5-disubstituted 1,3,4-oxadiazoles [J] . Mule Siva Nagi Reddy, Battula Sailaja Kumari, Velupula Ganapathi, RSC Advances . 2014,第102期

机译：10-樟脑磺酸（（+/-）-CSA）催化一锅合成新型的2,5-二取代1,3,4-恶二唑
2. 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
3. An efficient one-pot catalyzed synthesis of 2,5-disubstituted-1,3,4-oxadiazoles and evaluation of their antimicrobial activities [J] . Behalo Mohamed S. RSC Advances . 2016,第105期

机译：有效的单罐催化合成2,5-二取代-1,3,4-二唑和其抗微生物活性的评价
4. The Synthesis, Crystal Structure and Self-Organization of Molecules Containing 2,5-Bis(o-amino-phenyi)-1,3,4-Oxadiazoles Unit and N-Tos-L-Amino Acid Residues [C] . Hongwu Zhao International symposium for Chinese organic chemists . 2000

机译：含有2,5-双（O-氨基 - 酚）-1,3,4-二氧化唑单元和N-TOS-L-氨基酸残基的合成，晶体结构和自组织
5. Part I: 1,3,4-oxadiazoles in tandem Diels-Alder, 1,3-dipolar cycloaddition reactions: A rapid synthesis of vinca alkaloid motifs. Part II: Exceptionally potent inhibitors of fatty acid amide hydrolase [D] . Wilkie, Gordon David 2002

机译：第一部分：串联Diels-Alder中的1,3,4-恶二唑，1,3-偶极环加成反应：长春花生物碱基序的快速合成。第二部分：脂肪酸酰胺水解酶的超强抑制剂
6. An Efficient One-Pot Catalyzed Synthesis of 24-Disubstituted 5-Nitroimidazoles Displaying Antiparasitic and Antibacterial Activities [O] . Fanny Mathias, Youssef Kabri, Liliane Okdah, 2017

机译：有效的一锅催化合成的24-二取代的5-硝基咪唑显示出抗寄生虫和抗菌活性
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

10-Camphorsulfonic acid ((+/-)-CSA) catalyzed facile one-pot synthesis of a new class of 2,5-disubstituted 1,3,4-oxadiazoles

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