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Synthesis of beta-selenylated ketones via iodine-mediated selenylation/1,2-carbon migration sequences of alkenyl alcohols
- Authors
- Kim, Yubin; Kim, Dae Young
- Issue Date
- 6-Jun-2019
- Publisher
- Elsevier BV
- Keywords
- Selenylation; Iodine-mediated reaction; Semipinacol rearrangement; Alkenyl alcohols
- Citation
- Tetrahedron Letters, v.60, no.23, pp 1538 - 1542
- Pages
- 5
- Journal Title
- Tetrahedron Letters
- Volume
- 60
- Number
- 23
- Start Page
- 1538
- End Page
- 1542
- ISSN
- 0040-4039
- Abstract
- An iodine-mediated selenylation/1,2-carbon migration sequences of alkenyl alcohols is described. This approach provides a mild and operationally simple access to the synthesis of beta-selenated cyclic ketone derivatives from the coupling reaction of alkenyl alcohols with diselenides. (C) 2019 Elsevier Ltd. All rights reserved.
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Related Researcher
- Kim, Dae Young
- College of Natural Sciences (Department of Chemistry)