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Direct Synthesis of Polysubstituted Aldehydes via Visible-Light Catalysis.
Wu, Fengjin; Wang, Leifeng; Chen, Jiean; Nicewicz, David A; Huang, Yong.
Affiliation
  • Wu F; Key Laboratory of Chemical Genomics, School of Chemical Biology and Biotechnology, Peking University, Shenzhen Graduate School, Shenzhen, 518055, China.
  • Wang L; Key Laboratory of Chemical Genomics, School of Chemical Biology and Biotechnology, Peking University, Shenzhen Graduate School, Shenzhen, 518055, China.
  • Chen J; Shenzhen SynLED Technology Limited, 2-104, BIO-Incubator, Gaoxin C, 1st Ave., Shenzhen Hi-Tech Industrial Park, Nanshan, Shenzhen, 518057, China.
  • Nicewicz DA; Key Laboratory of Chemical Genomics, School of Chemical Biology and Biotechnology, Peking University, Shenzhen Graduate School, Shenzhen, 518055, China.
  • Huang Y; Key Laboratory of Chemical Genomics, School of Chemical Biology and Biotechnology, Peking University, Shenzhen Graduate School, Shenzhen, 518055, China.
Angew Chem Int Ed Engl ; 57(8): 2174-2178, 2018 02 19.
Article in En | MEDLINE | ID: mdl-29316099
ABSTRACT
Aldehydes are among the most versatile functional groups for synthetic chemistry. However, access to polysubstituted alkyl aldehydes is very limited and requires lengthy synthetic routes that involve multiple-step functional-group conversion. This paper reports a one-step synthesis of polysubstituted aldehydes from readily available olefin substrates using visible-light photoredox catalysis. Despite a number of competing reaction pathways, commercial styrenes react with vinyl ethers selectively in the presence of an acridinium salt photooxidant and a disulfide hydrogen-atom-transfer catalyst under blue LED irradiation. Alkyl aldehydes with different substitution patterns are prepared in good yields. This strategy can be applied to structurally sophisticated substrates.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Angew Chem Int Ed Engl Year: 2018 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Angew Chem Int Ed Engl Year: 2018 Document type: Article Affiliation country: China