Abstract
The asymmetric phase-transfer catalysis (PTC) is a flourishing field of contemporary synthetic organic chemistry, and this prominent methodology has been tremendously successful in enantioselective halogenations. Both electrophilic and nucleophilic reaction manifolds were enabled through the exploitation of highly ordered ion pairing and/or hydrogen-bonding interactions around a carefully designed chiral phase-transfer catalyst with an insoluble halogenating reagent as well as a suitable substrate. Fluorination has been the most fruitful, and encouraging results have also been documented with heavier halogens. This review surveys examples of various enantioselective halogenations via the asymmetric PTC from its beginning to prosperity over the past decade.
| Original language | English |
|---|---|
| Pages (from-to) | 896-911 |
| Number of pages | 16 |
| Journal | Bulletin of the Korean Chemical Society |
| Volume | 43 |
| Issue number | 7 |
| DOIs | |
| State | Published - Jul 2022 |
Bibliographical note
Publisher Copyright:© 2022 Korean Chemical Society, Seoul & Wiley-VCH GmbH.
Keywords
- enantioselectivity
- halogenation
- hydrogen bonding
- ion pairing
- phase-transfer catalysis