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通过三组分反应进行面部区域选择性合成新型生物活性螺吡咯烷/吡咯嗪-氧化吲哚衍生物作为潜在抗菌剂

Facial Regioselective Synthesis of Novel Bioactive Spiropyrrolidine/Pyrrolizine-Oxindole Derivatives via a Three Components Reaction as Potential Antimicrobial Agents.

作者信息

Hassaneen Huwaida M E, Eid Elshimaa M, Eid Hamid A, Farghaly Thoraya A, Mabkhot Yahia Nasser

机构信息

Chemistry Department, Faculty of Science, Cairo University, Giza 12613, Egypt.

Department of Chemistry, Faculty of Applied Science, Umm Al-Qura University, Makkah Almukkarramah 21514, Saudi Arabia.

出版信息

Molecules. 2017 Feb 26;22(3):357. doi: 10.3390/molecules22030357.

Abstract

This article presents the synthesis of new derivatives of spirooxindole-spiropiperidinone- pyrrolidines - and spirooxindole-spiropiperidinone-pyrrolizines - through a 1,3-dipolar cycloaddition reaction of azomethineylides generated from isatin, sarcosine, and l-proline, through a decarboxylative route with dipolarophile -. All of the newly synthesized compounds were evaluated for their antimicrobial activities and their minimum inhibitory concentration (MIC) against most of the test organisms. The tested compounds displayed excellent activity against all of the tested microorganisms.

摘要

本文介绍了通过异吲哚酮、肌氨酸和L-脯氨酸生成的甲亚胺叶立德经脱羧途径与亲偶极体发生1,3-偶极环加成反应,合成螺环氧化吲哚-螺环哌啶酮-吡咯烷类和螺环氧化吲哚-螺环哌啶酮-吡咯嗪类新衍生物的方法。对所有新合成的化合物进行了抗菌活性及其对大多数受试生物的最低抑菌浓度(MIC)评估。受试化合物对所有受试微生物均表现出优异的活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdba/6155345/53e85457f1ea/molecules-22-00357-sch001.jpg

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