Affiliation:
1. Department of Biophysical Chemistry Graduate School of Pharmaceutical Science Tohoku University 6–3 Aoba Sendai 980-8578 Japan
Abstract
AbstractHerein, we describe a KO‐t‐Bu catalyzed thiolation of β‐(hetero)arylethyl ethers through MeOH elimination to form (hetero)arylalkenes followed by anti‐Markovnikov hydrothiolation to afford linear thioethers. The system works well with a variety of β‐(hetero)arylethyl ethers, including electron‐deficient, electron‐neutral, electron‐rich, and branched substrates and a range of aliphatic and aromatic thiols.
Funder
Uehara Memorial Foundation
Tokyo Biochemical Research Foundation
Japan Agency for Medical Research and Development
Cited by
10 articles.
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