{"title":"Photo- and Electrochemical Organic Transformations Involving Radical Pathway: A Retrospection of Our Green-Chemistry-Inspired Synthetic Endeavours","authors":"Goutam Brahmachari","doi":"10.1055/s-0043-1775382","DOIUrl":null,"url":null,"abstract":"<p>This account summarises our recent efforts (2020 to mid-2024) in designing and developing a handful of promising organic transformations for accessing several diversely functionalized biologically relevant organic scaffolds by following the green-chemistry principles with a particular focus on the application of low-energy visible light and electrochemistry. Mechanistic studies of each of these reactions established the involvement of a radical pathway.</p> <p>1 Introduction</p> <p>2 Green-Inspired Organic Transformations</p> <p>2.1 Visible-Light-Driven Organic Synthesis</p> <p>2.1.1 Synthesis of Functionalized Dihydrofuro[3,2-<i>c</i>]chromenones</p> <p>2.1.2 Synthesis of Functionalized 2-(Aryl/alkylamino)-3-(aryl/alkylselanyl)naphthalene-1,4-diones and 2-(Arylamino)-3-(arylthio)naphthalene-1,4-diones</p> <p>2.1.3 Synthesis of Functionalized 6-(Arylthio/arylseleno)benzo[<i>a</i>]phenazin-5-ols</p> <p>2.1.4 Synthesis of Functionalized 3-(Alkyl/benzylthio)-4-hydroxy-2<i>H</i>-chromen-2-ones</p> <p>2.1.5 Synthesis of Functionalized 2-Hydroxy-3-oxo-2,3-dihydrobenzofuran-2-carboxamides and 2-Hydroxy-3-oxo-2,3-dihydrobenzofuran-2-carboxylates</p> <p>2.1.6 Synthesis of Functionalized 2-Hydroxyphenylated α-Ketoamides</p> <p>2.2 Electrochemical Organic Synthesis</p> <p>2.2.1 Synthesis of 3-Selenylated/Sulfenylated Derivatives of 2-Amino-1,4-naphthoquinones</p> <p>2.2.2 Synthesis of Functionalized 6-(Arylthio/Arylseleno)benzo[<i>a</i>]phenazin-5-ols</p> <p>2.2.3 Synthesis of Functionalized Alkyl 2-Hydroxy-3-oxo-2,3-dihydrobenzofuran-2-carboxylates</p> <p>3 Conclusions</p> ","PeriodicalId":22319,"journal":{"name":"Synlett","volume":"47 1","pages":""},"PeriodicalIF":1.7000,"publicationDate":"2024-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Synlett","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1055/s-0043-1775382","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0
Abstract
This account summarises our recent efforts (2020 to mid-2024) in designing and developing a handful of promising organic transformations for accessing several diversely functionalized biologically relevant organic scaffolds by following the green-chemistry principles with a particular focus on the application of low-energy visible light and electrochemistry. Mechanistic studies of each of these reactions established the involvement of a radical pathway.
1 Introduction
2 Green-Inspired Organic Transformations
2.1 Visible-Light-Driven Organic Synthesis
2.1.1 Synthesis of Functionalized Dihydrofuro[3,2-c]chromenones
2.1.2 Synthesis of Functionalized 2-(Aryl/alkylamino)-3-(aryl/alkylselanyl)naphthalene-1,4-diones and 2-(Arylamino)-3-(arylthio)naphthalene-1,4-diones
2.1.3 Synthesis of Functionalized 6-(Arylthio/arylseleno)benzo[a]phenazin-5-ols
2.1.4 Synthesis of Functionalized 3-(Alkyl/benzylthio)-4-hydroxy-2H-chromen-2-ones
2.1.5 Synthesis of Functionalized 2-Hydroxy-3-oxo-2,3-dihydrobenzofuran-2-carboxamides and 2-Hydroxy-3-oxo-2,3-dihydrobenzofuran-2-carboxylates
2.1.6 Synthesis of Functionalized 2-Hydroxyphenylated α-Ketoamides
2.2 Electrochemical Organic Synthesis
2.2.1 Synthesis of 3-Selenylated/Sulfenylated Derivatives of 2-Amino-1,4-naphthoquinones
2.2.2 Synthesis of Functionalized 6-(Arylthio/Arylseleno)benzo[a]phenazin-5-ols
2.2.3 Synthesis of Functionalized Alkyl 2-Hydroxy-3-oxo-2,3-dihydrobenzofuran-2-carboxylates
期刊介绍:
SYNLETT is an international journal reporting research results and current trends in chemical synthesis in short personalized reviews and preliminary communications. It covers all fields of scientific endeavor that involve organic synthesis, including catalysis, organometallic, medicinal, biological, and photochemistry, but also related disciplines and offers the possibility to publish scientific primary data.