<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8</volume><submitter>Yang Y</submitter><funding>National Natural Science Foundation of China</funding><pubmed_abstract>Quinoxaline derivatives demonstrate many distinguished chemical, biological, and physical properties and have a wide application in dyes, electroluminescent material, organic semiconductors, biological agents, etc. However, the synthesis of quinoxaline still suffers from several drawbacks, for instance, longer reaction time, unsatisfactory yields, and use of metal catalysts. Here, utilizing microdroplet-assisted reaction, we demonstrate the successive synthesis of several important quinoxaline derivatives. For case studies of 1H-indeno [1, 2-b] quinoxaline and 3,5-dimethyl-2-phenylquinoxaline, the present microdroplet approach can complete in milliseconds and the conversion rate reached 90% without adding any catalyst, which is considerably quicker and higher than conversional bulk-phase r</pubmed_abstract><journal>Frontiers in chemistry</journal><pagination>789</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7533680</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A High-Throughput Screening Method for Determining the Optimized Synthesis Conditions of Quinoxaline Derivatives Using Microdroplet Reaction.</pubmed_title><pmcid>PMC7533680</pmcid><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Mu X</pubmed_authors><pubmed_authors>Chen Z</pubmed_authors><pubmed_authors>Yang P</pubmed_authors><pubmed_authors>Tang B</pubmed_authors><pubmed_authors>Niu L</pubmed_authors><pubmed_authors>Li R</pubmed_authors><pubmed_authors>Niu W</pubmed_authors></additional><is_claimable>false</is_claimable><name>A High-Throughput Screening Method for Determining the Optimized Synthesis Conditions of Quinoxaline Derivatives Using Microdroplet Reaction.</name><description>Quinoxaline derivatives demonstrate many distinguished chemical, biological, and physical properties and have a wide application in dyes, electroluminescent material, organic semiconductors, biological agents, etc. However, the synthesis of quinoxaline still suffers from several drawbacks, for instance, longer reaction time, unsatisfactory yields, and use of metal catalysts. Here, utilizing microdroplet-assisted reaction, we demonstrate the successive synthesis of several important quinoxaline derivatives. For case studies of 1H-indeno [1, 2-b] quinoxaline and 3,5-dimethyl-2-phenylquinoxaline, the present microdroplet approach can complete in milliseconds and the conversion rate reached 90% without adding any catalyst, which is considerably quicker and higher than conversional bulk-phase r</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020</publication><modification>2025-04-18T13:20:29.223Z</modification><creation>2020-11-22T09:49:15Z</creation></dates><accession>S-EPMC7533680</accession><cross_references><pubmed>33195024</pubmed><doi>10.3389/fchem.2020.00789</doi></cross_references></HashMap>