Visible-Light-Induced Arylthiofluoroalkylations of Unactivated Heteroaromatics and Alkenes
- Authors
- Choi, Yeojin; Yu, Chunghyeon; Kim, Jun Soo; Cho, Eun Jin
- Issue Date
- Jul-2016
- Publisher
- AMER CHEMICAL SOC
- Citation
- ORGANIC LETTERS, v.18, no.13, pp 3246 - 3249
- Pages
- 4
- Journal Title
- ORGANIC LETTERS
- Volume
- 18
- Number
- 13
- Start Page
- 3246
- End Page
- 3249
- URI
- https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/6745
- DOI
- 10.1021/acs.orglett.6b01495
- ISSN
- 1523-7060
1523-7052
- Abstract
- Visible-light-induced arylthiofluoroalkylations of unactivated heteroaromatics and alkenes have been developed utilizing readily available arylthiofluoroalkyl sources. This method enables simultaneous installation of sulfur and fluoroalkyl moieties, two important functional groups, which demonstrates its potential use for late-stage modifications in the synthesis of functional molecules. This method can be easily utilized to fine-tune the properties of lead molecules in drug development by controlling the number of fluorine atoms in the reagents.
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Collections - College of Natural Sciences > Department of Chemistry > 1. Journal Articles
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